- Open Access
Pluripotency and its layers of complexity
Cell Regeneration volume 1, Article number: 7 (2012)
Pluripotency is depicted by a self-renewing state that can competently differentiate to form the three germ layers. Different stages of early murine development can be captured on a petri dish, delineating a spectrum of pluripotent states, ranging from embryonic stem cells, embryonic germ cells to epiblast stem cells. Anomalous cell populations displaying signs of pluripotency have also been uncovered, from the isolation of embryonic carcinoma cells to the derivation of induced pluripotent stem cells. Gaining insight into the molecular circuitry within these cell types enlightens us about the significance and contribution of each stage, hence deepening our understanding of vertebrate development. In this review, we aim to describe experimental milestones that led to the understanding of embryonic development and the conception of pluripotency. We also discuss attempts at exploring the realm of pluripotency with the identification of pluripotent stem cells within mouse teratocarcinomas and embryos, and the generation of pluripotent cells through nuclear reprogramming. In conclusion, we illustrate pluripotent cells derived from other organisms, including human derivatives, and describe current paradigms in the comprehension of human pluripotency.
Pluripotency is denoted by the capacity of a self-renewing cell to develop into the three germ layers. The conception of pluripotency emerged in the Classical Greek period where rudimentary methods were employed to examine the development of organs within chick embryos . These observations were left unexplored for two thousand years and awareness was rekindled in the Renaissance period where the invention of the microscope enhanced the resolution of developing embryos. This elicited the establishment of several landmark discoveries and escalated our understanding of vertebrate developmental processes.
The first testimony of pluripotency on a petri dish was portrayed using inbred strains of mice. Spontaneous incidences of teratocarinomas arose at low frequencies in 129 strain of mice . This led to the isolation of pluripotent stem cells that were able to regenerate tumours consisting of the three germ layers . Subsets of pluripotent cell populations came in quick succession, where various cell types within the mouse embryo were isolated and snapshots of distinct developmental stages were captured [4–9]. Other than naturally occurring instances in normal development, artificial states that are reflective of pluripotency have been accomplished. Cells from developing Rana pipiens embryos were demonstrated to undergo nuclear transplantation and revert to a primitive state capable of developing into an entire organism . This highlighted the capacity of a non-pluripotent cell to reset its epigenetic marks and convert to a pluripotent derivative. Termed as nuclear reprogramming, these findings were extended in mice and further exemplified in alternative methods [11–14].
The easy manipulation and cultivation of mouse pluripotent stem cells have provided a convenient platform to study the independent developmental stages. Furthermore, comparison of these pluripotent states and their necessary environmental milieu for sustenance provides indications of developmental cues (reviewed by ). Pluripotent stem cells from various non-rodent and primate species have been achieved either directly from embryos or through nuclear reprogramming, but none are truly reflective of mouse embryonic stem cells that display germline competence (reviewed by Nichols and Smith, 2009c) . Recent studies suggest that conventional human pluripotent cells resemble mouse epiblast stem cells more closely than mouse embryonic stem cells , indicating the possibility of a primitive subset of human pluripotent stem cells which have not been clearly delineated.
This review aims to address these concerns by first describing the milestones established through the study of vertebrate development and pluripotency. This will be followed by the illustration of extrinsic signals and molecular pathways associated to pluripotency. By way of introducing pluripotent stem cells achieved from alternative organisms, we compare the differences between human and mouse pluripotent stem cells and describe recent inferences on a distinct state of human pluripotency.
History of vertebrate development
The development of vertebrates involves the orchestration of a series of steps in a tightly regulated process that determines cell lineage specification into endodermal, ectodermal and mesodermal derivatives. Imprinted into the operational dogma of modern developmental biology, conception of these notions has been accompanied by a history of key observations and controversies.
Originating from examinations of the chick embryo, Aristotle witnessed the development of a palpitating heart, head and eyes, laying ink on a clean palette of embryology . With the proposition of epigenesis, he described development as a sequential process involving the formation of organs to construct a complete organism. Almost two thousand years after these initial recordings, the field was reawakened and the mechanisms behind these phenomena were questioned. To examine the root of development, Girolamo Fibrici performed dissections on cadavers of pregnant mammals, providing comparisons between anatomical structures of uteri . This work was advanced by his student William Harvey who hypothesised the presence of female germ cells within uteri that hold the capacity to constitute a new organism (). Furthermore, identification of budding and subdivision during primary stages of embryonic development of the chick led him to be a strong advocate of epigenesis. These findings revived Aristotle’s theory and provoked collision against preformation views. Preformationism was held as the dominant perception of development, and describes the existence of a miniature organism that expands without increasing complexity within the germ cell. Although epigenesis perceptions were resurrected, it was not received warmly. Transformation of the field of development biology was invoked by subsequent experiments led by Caspar Frederich Wolff and Karl Ernst von Baer. Using plants as a surrogate organism for study, Wolff explained the ability of differentiated plant root to regenerate a new organism. This study was traversed to chick embryos where Wolff studied the formation of embryonic kidneys . Building on the scaffold of information uncovered by his predecessors, von Baer discovered the presence of primitive germ cells and ultimately eclipsed any influence of preformationism .
Beginnings of the notion of pluripotency
Delineating vertebrate developmental processes proposes the presence of pluripotent cells which participate in the contribution of the cellular entirety of an adult organism. The first inkling of pluripotency was established by Hans Driesch who demonstrated that isolation of individual cells within 2-cell embryos culminated in the generation of two small complete larvae . In parallel, Hans Spemann validated the ability of detached cells within 2-cell newt embryos to develop into intact organisms . As Spemann was poised with micro-surgical skills, he extended his findings in embryology through the constriction of developing embryos using baby hair. By restricting the position of the nucleus to one side of the cytoplasm, development of the embryo into its 16-cell state would result in the escape of one cell past the noose, into the opposite end. This led to the formation of twin larvae, suggesting the pluripotent capacity of cells within the developing embryo. These findings illuminated a new era of embryological study and unravelled avenues for the study of pluripotency.
Embryonic carcinoma cells
To reinforce the notion of pluripotency, pluripotent cells have been successfully established on the Petri dish. Teratocarcinomas are tumours discovered in humans and mice ([2, 23]. Inspection of these cellular masses reveals the presence of a plethora of organised structures, including teeth, fingers and hair, suggesting the presence of pluripotent cells within the tumour. This was corroborated through the determination that intraperitoneal injection of a single cell could generate teratocarcinoma consisting of an array of differentiated tissues . Likewise, grafting of mouse embryos into adult mice also leads to the formation of teratomas, reinforcing the existence of all-encompassing cells ([24, 25]). Teratomas in both contexts have been successfully maintained in culture [26–29]. Designated as embryonic carcinoma (EC) cells, these cells exhibit pluripotent properties including the ability to form teratomas in immune-compromised mice and serve as the first platform to study embryonic development of mice in vitro.
Embryonic stem cells
Soon after, the inner cell mass of mouse blastocysts was demonstrated to be sustained on a petri dish, recapitulating an early developmental event in vitro [5, 6]. Labelled as embryonic stem (ES) cells, these cells were competent at contributing to the three germ layers in teratomas, when injected into immune-compromised or syngenic mice. Furthermore, re-introduction of these cells into the mouse blastocyst led to the formation of high percentage chimeras, indicating their ability to participate in normal murine development, a property not frequently shared with EC cells. To satisfy stringent pluripotent stipulations, ES cells were also studied for their ability to contribute to the germline and an intact embryo. The former was approached through the cross of chimeras to phenotypically distinct wildtype mice , whereas the latter was addressed through tetraploid complementation assays [31, 32].
Amenable to modifications, ES cells embody a useful tool for genetic alterations (reviewed in ). With the elucidation of the genetic composition of the mouse in 2002 , the genomic content of ES cells has been frequently disrupted in a precise fashion to study gene function. The capacity for germline transmission results in the establishment of intact mice harbouring any desired genetic mutation in the germline [35–38].
Epiblast stem cells
ES cells represent a subset of cells isolated from the epiblast in pre-implantation blastocysts and depict a primitive developmental stage of the developing embryo. To recapitulate late phases, two independent groups have segregated the columnar epithelial epiblast of the early post-implantation embryo and cultivated it on a petri dish [4, 9]. Termed as Epiblast stem cells (EpiSCs), they behave distinctly from ES cells and are rarely able to generate chimeras. However, both ES cells and EpiSCs are competent in multi-lineage differentiation, where injection of these cells into immune-compromised mice results in the development of teratomas comprised of tissue types characteristic of the three germ layers [4, 9].
Examination of the molecular circuitry within these cells revealed some similarities to ES cells, where the core transcriptional machinery consisting of Oct4, Sox2 and Nanog was expressed [39–41]. However, ES cells and EpiSCs exhibit disparities in transcript and epigenetic levels of markers associated to the inner cell mass and early germ layers , highlighting distinctions in their original developmental stages.
Embryonic germ cells
Pluripotent stem cells divergent from the mouse blastocyst were first derived from primordial germ cells (PGCs) [7, 8]. Emergent at 7 days post coitum (dpc), these cells are represented by a small population of alkaline-phosphatase positive cells . In a span of six days, these cells undergo extensive proliferation every 16 hours to comprise of 25,000 PGCs , and eventually reside in either the testis or ovary of the mouse.
Extraction of PGCs at 8.5-12.5 dpc from the posterior fragment of the embryo and cultivation in the presence of soluble factors such as leukemia inhibitory factor (LIF), steel factor (SF) and fibroblast growth factor (FGF), results in a population of cells that exhibits self-renewal and limitless proliferation ([7, 8, 44, 45]). Coined as embryonic germ (EG) cells, these cells resemble ES cells and are capable of generating chimeras and contributing to the mouse germline [7, 46, 47].
Artificial states of pluripotency
Historical perspectives on the study of vertebrate development illuminated the remarkable capacity of a fertilized oocyte to generate a complete organism. This led to the advent of nuclear reprogramming, denoted by the transition between unrelated cell types triggered by switches in gene patterns. Introduction of a somatic cell nucleus into an enucleated oocyte results in the re-establishment of epigenetic marks, allowing the hybrid cell to generate an organism (; [48, 49]). Termed as Somatic Cell Nuclear Transfer (SCNT), this technique has proved effective across species [11, 50], but is subject to technical competence and coordinated mitotic cycles (reviewed by ).
A similar phenomenon is observed upon the fusion of pluripotent stem cells and somatic cells. The environmental milieu arising from the pluripotent cell seizes control of the cellular transcriptional machinery and leads to the silencing of somatic markers in the fusion cells. The resultant heterokaryon is tetraploid but able to differentiate into all three germ layers [14, 52].
Recently, ectopic expression of four transcription factors was described to revert somatic cells to a pluripotent state . For the ease of nomenclature, these resultant cells were termed as induced pluripotent stem (iPS) cells. Mouse iPS cells are similar to mouse ES cells, and are capable of generating chimeras and contributing to the germline . Traversed across species, human iPS cells have since been obtained [54, 55]. The ability to generate patient specific iPS cells highlights its potential for cell therapy, drug screening and disease modelling (reviewed by ). Comprehensive studies of iPS cells and ES cells reveal minute differences in phosphoproteomic and transcriptomic components that were statistically disregarded . However, epigenomic analysis at high resolution expose subtle differences between iPS cells and ES cells [58, 59] and continuous in vitro culture could incur genomic aberrations [58, 60, 61]. These discrepancies could account for functional disparities such as epigenetic memory [62–64] and immunogenicity , surmising potential for improvement in the derivation of iPS cells which possess qualities that are identical to ES cells.
Chemicals and pathways associated with murine pluripotent stem cells
Pluripotent cells exist in a fleeting manner within the mouse embryo, placing emphasis on the remarkable extension of their life in culture. Supporting chemicals or matrix are necessary for the maintenance of pluripotency in culture, as exemplified in the reliance on fibroblasts and serum in primary studies describing ES cells, EC cells and EG cells, suggesting a non-cell autonomous mechanism in self-renewal. Extrication of components that support pluripotency, in concert with our current understanding of developmental pathways, can lead to the improvement of growth parameters of pluripotent cells, and augment our knowledge on embryonic development.
Stemming from the discovery that medium conditioned by Buffalo rat liver cells was sufficient to retain pluripotency , the active component necessary for this phenomenon was narrowed down to leukemia inhibitory factor (LIF) [67, 68]. The importance of LIF has been portrayed by its obligatory need in the culture medium , acting through gp130 and the recruitment of JAK kinase and STAT3 [70, 71]. The ability of LIF to maintain pluripotency in culture is mirrored in a physiological context, where LIF and gp130 are expressed in early embryos and during diapause .
Although LIF/gp130 and their related pathways are pivotal in the maintenance of pluripotency, the use of chemically defined basal media supplemented with N2, B27 and LIF is unable to impede differentiation of ES cells into neuronal derivatives . This propensity to differentiate can be restrained by the addition of bone morphogenetic protein (BMP), an anti-neural factor in vertebrate development . Functioning through Inhibitor of differentiation (Id), BMP together with LIF are sufficient to drive ES cells into self-renewal without differentiation .
Interaction between LIF and gp130 triggers a conflicting response, where both the JAK/STAT and ERK1/2 pathways are activated [75, 76]. As the latter stimulates differentiation, ERK or FGF inhibitors were demonstrated to circumvent this impediment and support the maintenance of ES cells . Activation of the Wnt pathway through the inhibition of GSK3β also assists in the sustenance of an undifferentiated state. The effects of ERK and GSK3β inhibition (2i) are compounded when used in combination, and results in a homogenous population of primitive cells designated as ground state pluripotency . Mirroring this in vivo, addition of 2i to early mouse embryos in culture causes an expansion of the Nanog-expressing epiblast at the expense of the hypoblast and trophoectoderm compartments . Growth media containing 2i and LIF has also made it possible to derive ES cells from mouse strains, such as CBA and NOD, and rats, which have been recalcitrant to previous methods [77, 80–82].
The culture conditions of EpiSCs are distinct from ES cells. FGF and Activin are necessary to preserve EpiSCs [4, 9], whereas the addition of 2i and LIF generally results in cell differentiation or death . In contrast, addition of an Activin inhibitor led to widespread differentiation, suggesting reliance on Nodal/Activin signalling .
The disparities reflected by dissimilar developmental potential and growth conditions of mouse ES cells and EpiSCs has led to the notion of naïve and primed pluripotency (Nichols and Smith, 2009c). Originating from the pre-implantation epiblast, ES cells display complete pluripotent potential and are capable of germline contribution. In contrast, EpiSCs derived from the post-implantation epiblast are incapable of neither somatic nor germline contribution, exhibiting limited pluripotent potential.
Classification of naïve and primed pluripotency has been strengthened by the analysis of X-chromosome inactivation (XCI). XCI is a process where one X chromosome in female diploid cells is inactivated, resulting in the reduction of most X-linked transcripts to comparable levels between males and females (; reviewed by ). Apart from EpiSCs, mouse pluripotent cells (ES, EC, EG, iPS cells) display two copies of active X chromosomes [86–88]. This is reminiscent of pre-implantation epiblasts which possess two active X chromosomes and hold the capacity to derive complete organisms, exemplifying naïve pluripotency [89, 90]. In contrast, EpiSCs exhibit XCI  or primed pluripotency and represent post-implantation epiblasts where XCI begins and the capacity to form whole organisms is lost.
Establishment of ES cells from other species
After successful isolation and culture of mouse ES cells, there have been several attempts at engineering an equivalent in various species, including rodents such as hamsters and rats [80, 81, 91], non-rodents such as rabbits, minks, chickens, pigs and cows [92–98], and primates such as rhesus monkeys and the common marmosets [99, 100].
Heightened interest in the generation of an array of pluripotent stem cells can be attributed to its potential to differentiate into an array of cell types, representative of the three germ layers. Application of this technology to humans illuminates the possibility of regenerative medicine. To address this, human ES cells were derived from cleavage stage human embryos that were acquired from in vitro fertilization donors .
With the successful establishment of human ES cells, much effort has been directed at understanding the pathways involved in maintaining the pluripotent cells in culture and modifications to growth conditions of human ES cells have since been implemented. Unlike mouse ES cells, LIF signalling is not sufficient to sustain undifferentiated human ES cells [102, 103]. In addition, BMP4 triggers trophectoderm differentiation in human ES cells [104, 105]. Instead, FGF and Nodal/Activin signalling pathways have been implicated in the self-renewal of human ES cells, reminiscent of EpiSCs [106–109]. Furthermore, comparison of gene expression patterns and XCI further supports the resemblance between human ES cells and EpiSCs .
Following the inception of transcription factor induced reprogramming, an array of human somatic cell types have been competently reprogrammed to derive human iPS cells [54, 55, 111, 112]. Human iPS cells represent an attractive source of patient-specific pluripotent cells and evade ethical concerns faced by the usage of human ES cells. Cultivated in a similar environment to human ES cells, human iPS cells display close resemblance when protein and epigenetic signatures are compared [57, 58], hence are also likened to EpiSCs.
Differences between human and mouse ES cells: naïve and primed pluripotency
The similarities between human pluripotent cells (human ES cells and iPS cells) and primed pluripotent mouse EpiSCs propose the possible existence of an unexplored naïve human pluripotent state reminiscent of mouse ES cells. Using human embryos, it has been recently demonstrated that introduction of inhibitors against FGF, ERK or GSK3 did not reduce the Nanog-expressing epiblast compartment, highlighting a stark contrast to conventional human pluripotent cells which readily differentiate in similar conditions [113, 114]. An additional study which traced the origin of human ES cells derived from human blastocysts noted that the establishment of human ES cell lines required the transition into a post-ICM intermediate displaying X-inactivation ().
Murine EpiSCs can be converted into ES cells with the ectopic expression of Klf2, Klf4, Nr5a2, or the addition of 2i and LIF ([83, 116], ). Likewise, human ES cells have been manipulated to phenotypically resemble mouse ES cells . Using iPS cell technology, similar cellular states have been achieved using chemical cocktails or various transgenic combinations [88, 118–120]. In some of these findings, both copies of X chromosomes are active, suggesting the possible attainment of naïve pluripotency. Strikingly, these novel pluripotent states rely on continuous transgenic expression, and only one study established human iPS cells that exhibited XCI reversion and transgene independence .
The study of pluripotency has amassed a wealth of information (Figure 1), from the discovery of nuclear reprogramming in the 1952, to the isolation of mouse ES cells and EpiSCs in 1981 and 2007 respectively. As the first vertebrate model organism used to study pluripotency, our understanding of the various stages during mouse embryonic development has thrived. Translating this knowledge to the developmental processes in other organisms may shed light on species-specific embryological properties, or offer refinements to the strategies employed for the study of development.
The identification of human pluripotent cells and their comparison to murine counterparts is one such example. Disparate chemical components within the growth media plays a critical role in the observed differences between primed human pluripotent cells and naïve mouse ES cells. The generation of mouse ES cells from the inner cell mass of the blastocyst involves the acquisition of new genetic profiles associated to self-renewal, epigenetic regulation and arrest of normal development , emphasising the influence of culture conditions on the establishment of cell lines. Furthermore, growth conditions can be manipulated to derive pluripotent cell lines from blastocysts which are distinct from mouse ES cells and EpiSCs , and EpiSC-like derivatives from fibroblasts using the conventional cocktail of reprogramming factors .
Although conventional human pluripotent stem cells resemble mouse EpiSCs closely, there exist differences between the two. EpiSCs express cell surface marker SSEA-1, whereas conventional human ES cells and iPS cells display SSEA3/4 (; reviewed by ). In addition, human ES cells, express pluripotency markers DPPA3, KLF4 and REX1, unlike EpiSCs [39, 110].
As the study of human pluripotency is in its infancy, parallel studies in mouse models can only serve as a guide and may not faithfully recapitulate the physiological events which occur during human development. However, recent pieces of evidence suggest the existence of a naïve state of pluripotency and may surmount difficulties met with FGF-dependent human ES cell and iPS cells. These include susceptibility to harsh dissociation, inability to survive in single cell suspension and genomic instability [125–130]. In conclusion, there remains much to be unearthed for the full elucidation of human embryonic development and further experiments are essential to uncover the proposed subset of naïve pluripotent stem cells.
This article highlights advancements in the study of pluripotency, evolving from primary embryological experiments, to the recapitulation of an array of pluripotent states in vitro. Murine ES cells were first reported in 1981  and represented an amenable and convenient platform to study developmental pathways and the sustenance of pluripotency. The identification of EG cells, EpiSCs and iPS cells led to the comprehension of various developmental stages. It was only in 1998 that success was met with human ES cells . Armed with 17 more years of research, mouse pluripotent states serve as a reference point when delineating human pluripotency. With the advent of iPS cells and sophisticated technical resources, knowledge garnered from the study of human ES cells and iPS cells will continue to amass exponentially, addressing our concerns on naïve pluripotency.
- ES cells:
embryonic stem cells
- EC cells:
embryonic carcinoma cells
Epiblast stem cells
- EG cells:
embryonic germ cells
- iPS cells:
induced pluripotent stem cells
leukemia inhibitory factor
fibroblast growth factor
Bone morphogenetic protein
Primordial germ cell.
Aristotle: Generation of Animals. Harvard University Press, Cambridge, MA; 1979.
Stevens LC, Little CC: Spontaneous Testicular Teratomas in an Inbred Strain of Mice. Proc Natl Acad Sci USA 1954,40(11):1080–1087. 10.1073/pnas.40.11.1080
Kleinsmith LJ, Pierce GB Jr: Multipotentiality of Single Embryonal Carcinoma Cells. Cancer Res 1964, 24: 1544–1551.
Brons IG, Smithers LE, Trotter MW, Rugg-Gunn P, Sun B, de Sousa Lopes SM C, Howlett SK, Clarkson A, Ahrlund-Richter L, Pedersen RA, et al.: Derivation of pluripotent epiblast stem cells from mammalian embryos. Nature 2007,448(7150):191–195. 10.1038/nature05950
Evans MJ, Kaufman MH: Establishment in culture of pluripotential cells from mouse embryos. Nature 1981,292(5819):154–156. 10.1038/292154a0
Martin GR: Isolation of a pluripotent cell line from early mouse embryos cultured in medium conditioned by teratocarcinoma stem cells. Proc Natl Acad Sci USA 1981,78(12):7634–7638. 10.1073/pnas.78.12.7634
Matsui Y, Zsebo K, Hogan BL: Derivation of pluripotential embryonic stem cells from murine primordial germ cells in culture. Cell 1992,70(5):841–847. 10.1016/0092-8674(92)90317-6
Resnick JL, Bixler LS, Cheng L, Donovan PJ: Long-term proliferation of mouse primordial germ cells in culture. Nature 1992,359(6395):550–551. 10.1038/359550a0
Tesar PJ, Chenoweth JG, Brook FA, Davies TJ, Evans EP, Mack DL, Gardner RL, McKay RD: New cell lines from mouse epiblast share defining features with human embryonic stem cells. Nature 2007,448(7150):196–199. 10.1038/nature05972
Briggs R, King TJ: Transplantation of Living Nuclei From Blastula Cells into Enucleated Frogs' Eggs. Proc Natl Acad Sci USA 1952,38(5):455–463. 10.1073/pnas.38.5.455
McGrath J, Solter D: Nuclear transplantation in the mouse embryo by microsurgery and cell fusion. Science (New York, NY 1983,220(4603):1300–1302. 10.1126/science.6857250
Tada M, Takahama Y, Abe K, Nakatsuji N, Tada T: Nuclear reprogramming of somatic cells by in vitro hybridization with ES cells. Curr Biol 2001,11(19):1553–1558. 10.1016/S0960-9822(01)00459-6
Takahashi K, Yamanaka S: Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors. Cell 2006,126(4):663–676. 10.1016/j.cell.2006.07.024
Ying QL, Nichols J, Evans EP, Smith AG: Changing potency by spontaneous fusion. Nature 2002,416(6880):545–548. 10.1038/nature729
Ng HH, Surani MA: The transcriptional and signalling networks of pluripotency. Nat Cell Biol 2011,13(5):490–496. 10.1038/ncb0511-490
Nichols J, Smith A: Naive and primed pluripotent states. Cell Stem Cell 2009,4(6):487–492. 10.1016/j.stem.2009.05.015
Fibrici G: De Formatione Ovi, et Pulli Tractatus Accuratissimus: Patavii [Padua]: ex Officina Aloysii Bencii Bibliopolae. 1621.
Harvey W: Exercitationes de generatione animalium: Hagae Comitis, apud A. Leers; 1680:1651.
Wolff CF: Theoria generationis: Typis et sumtu Io. Christ. Hendel; 1774.
von Baer KE: De ovi mammalium et hominis genesi: Sumptibus L. Vossii. 1827.
Driesch H: Analytische theorie der organischen entwicklung. Leipzig, W. Engelmann; 1894.
Spemann H: Die Entwicklung seitlicher und dorso-ventraler Keimhalften bei verzogerter Kernversogung. Z Wiss Zool 1928, 132: 105–134.
Giovanel BC, Stehlin JS, Williams LJ: Heterotransplantation of Human Malignant-Tumors in Nude Thymusless Mice .2. Malignant-Tumors Induced by Injection of Cell-Cultures Derived from Human Solid Tumors. J Natl Cancer I 1974,52(3):921–930.
Solter D, Skreb N, Damjanov I: Extrauterine growth of mouse egg-cylinders results in malignant teratoma. Nature 1970,227(5257):503–504. 10.1038/227503a0
Stevens LC: The development of transplantable teratocarcinomas from intratesticular grafts of pre- and postimplantation mouse embryos. Dev Biol 1970,21(3):364–382. 10.1016/0012-1606(70)90130-2
Evans MJ: The isolation and properties of a clonal tissue culture strain of pluripotent mouse teratoma cells. J Embryol Exp Morphol 1972,28(1):163–176.
Kahan BW, Ephrussi B: Developmental potentialities of clonal in vitro cultures of mouse testicular teratoma. J Natl Cancer I 1970,44(5):1015–1036.
Martin GR, Evans MJ: The morphology and growth of a pluripotent teratocarcinoma cell line and its derivatives in tissue culture. Cell 1974,2(3):163–172. 10.1016/0092-8674(74)90090-7
Rosenthal MD, Wishnow RM, Sato GH: In vitro growth and differetiation of clonal populations of multipotential mouse clls derived from a transplantable testicular teratocarcinoma. J Natl Cancer I 1970,44(5):1001–1014.
Bradley A, Evans M, Kaufman MH, Robertson E: Formation of germ-line chimaeras from embryo-derived teratocarcinoma cell lines. Nature 1984,309(5965):255–256. 10.1038/309255a0
Nagy A, Gocza E, Diaz EM, Prideaux VR, Ivanyi E, Markkula M, Rossant J: Embryonic stem cells alone are able to support fetal development in the mouse. Development 1990,110(3):815–821.
Nagy A, Rossant J, Nagy R, Abramow-Newerly W, Roder JC: Derivation of completely cell culture-derived mice from early-passage embryonic stem cells. Proc Natl Acad Sci U S A 1993,90(18):8424–8428. 10.1073/pnas.90.18.8424
Evans M: Discovering pluripotency: 30 years of mouse embryonic stem cells. Nature Rev Mol Cell Biol 2011,12(10):680–686. 10.1038/nrm3190
Waterston RH, Lindblad-Toh K, Birney E, Rogers J, Abril JF, Agarwal P, Agarwala R, Ainscough R, Alexandersson M, An P, et al.: Initial sequencing and comparative analysis of the mouse genome. Nature 2002,420(6915):520–562. 10.1038/nature01262
Kuehn MR, Bradley A, Robertson EJ, Evans MJ: A potential animal model for Lesch-Nyhan syndrome through introduction of HPRT mutations into mice. Nature 1987,326(6110):295–298. 10.1038/326295a0
Skarnes WC, Rosen B, West AP, Koutsourakis M, Bushell W, Iyer V, Mujica AO, Thomas M, Harrow J, Cox T, et al.: A conditional knockout resource for the genome-wide study of mouse gene function. Nature 2011,474(7351):337–342. 10.1038/nature10163
Smithies O, Gregg RG, Boggs SS, Koralewski MA, Kucherlapati RS: Insertion of DNA sequences into the human chromosomal beta-globin locus by homologous recombination. Nature 1985,317(6034):230–234. 10.1038/317230a0
Thomas KR, Capecchi MR: Site-directed mutagenesis by gene targeting in mouse embryo-derived stem cells. Cell 1987,51(3):503–512.
Boyer LA, Lee TI, Cole MF, Johnstone SE, Levine SS, Zucker JP, Guenther MG, Kumar RM, Murray HL, Jenner RG, et al.: Core transcriptional regulatory circuitry in human embryonic stem cells. Cell 2005,122(6):947–956. 10.1016/j.cell.2005.08.020
Loh YH, Wu Q, Chew JL, Vega VB, Zhang W, Chen X, Bourque G, George J, Leong B, Liu J, et al.: The Oct4 and Nanog transcription network regulates pluripotency in mouse embryonic stem cells. Nature Genet 2006,38(4):431–440. 10.1038/ng1760
Wang J, Rao S, Chu J, Shen X, Levasseur DN, Theunissen TW, Orkin SH: A protein interaction network for pluripotency of embryonic stem cells. Nature 2006,444(7117):364–368. 10.1038/nature05284
Ginsburg M, Snow MH, McLaren A: Primordial germ cells in the mouse embryo during gastrulation. Development 1990,110(2):521–528.
Tam PP, Snow MH: Proliferation and migration of primordial germ cells during compensatory growth in mouse embryos. Journal of embryology and experimental morphology 1981, 64: 133–147.
Godin I, Deed R, Cooke J, Zsebo K, Dexter M, Wylie CC: Effects of the steel gene product on mouse primordial germ cells in culture. Nature 1991,352(6338):807–809. 10.1038/352807a0
Matsui Y, Toksoz D, Nishikawa S, Williams D, Zsebo K, Hogan BL: Effect of Steel factor and leukaemia inhibitory factor on murine primordial germ cells in culture. Nature 1991,353(6346):750–752. 10.1038/353750a0
Labosky PA, Barlow DP, Hogan BL: Mouse embryonic germ (EG) cell lines: transmission through the germline and differences in the methylation imprint of insulin-like growth factor 2 receptor (Igf2r) gene compared with embryonic stem (ES) cell lines. Development 1994,120(11):3197–3204.
Stewart CL, Gadi I, Bhatt H: Stem cells from primordial germ cells can reenter the germ line. Developmental biology 1994,161(2):626–628. 10.1006/dbio.1994.1058
Gurdon JB: The developmental capacity of nuclei taken from intestinal epithelium cells of feeding tadpoles. Journal of embryology and experimental morphology 1962, 10: 622–640.
Gurdon JB, Elsdale TR, Fischberg M: Sexually mature individuals of Xenopus laevis from the transplantation of single somatic nuclei. Nature 1958,182(4627):64–65. 10.1038/182064a0
Wilmut I, Schnieke AE, McWhir J, Kind AJ, Campbell KH: Viable offspring derived from fetal and adult mammalian cells. Nature 1997,385(6619):810–813. 10.1038/385810a0
Egli D, Birkhoff G, Eggan K: Mediators of reprogramming: transcription factors and transitions through mitosis. Nature Rev Molecular Cell biol 2008,9(7):505–516. 10.1038/nrm2439
Cowan CA, Atienza J, Melton DA, Eggan K: Nuclear reprogramming of somatic cells after fusion with human embryonic stem cells. Science (New York, NY 2005,309(5739):1369–1373. 10.1126/science.1116447
Okita K, Ichisaka T, Yamanaka S: Generation of germline-competent induced pluripotent stem cells. Nature 2007,448(7151):313–317. 10.1038/nature05934
Takahashi K, Tanabe K, Ohnuki M, Narita M, Ichisaka T, Tomoda K, Yamanaka S: Induction of pluripotent stem cells from adult human fibroblasts by defined factors. Cell 2007,131(5):861–872. 10.1016/j.cell.2007.11.019
Yu J, Vodyanik MA, Smuga-Otto K, Antosiewicz-Bourget J, Frane JL, Tian S, Nie J, Jonsdottir GA, Ruotti V, Stewart R, et al.: Induced pluripotent stem cell lines derived from human somatic cells. Science (New York, NY 2007,318(5858):1917–1920. 10.1126/science.1151526
Wu SM, Hochedlinger K: Harnessing the potential of induced pluripotent stem cells for regenerative medicine. Nature cell biology 2011,13(5):497–505. 10.1038/ncb0511-497
Phanstiel DH, Brumbaugh J, Wenger CD, Tian S, Probasco MD, Bailey DJ, Swaney DL, Tervo MA, Bolin JM, Ruotti V, et al.: Proteomic and phosphoproteomic comparison of human ES and iPS cells. Nature Methods 2011,8(10):821–827. 10.1038/nmeth.1699
Lister R, Pelizzola M, Kida YS, Hawkins RD, Nery JR, Hon G, Antosiewicz-Bourget J, O'Malley R, Castanon R, Klugman S, et al.: Hotspots of aberrant epigenomic reprogramming in human induced pluripotent stem cells. Nature 2011,471(7336):68–73. 10.1038/nature09798
Stadtfeld M, Apostolou E, Akutsu H, Fukuda A, Follett P, Natesan S, Kono T, Shioda T, Hochedlinger K: Aberrant silencing of imprinted genes on chromosome 12qF1 in mouse induced pluripotent stem cells. Nature 2010,465(7295):175–181. 10.1038/nature09017
Gore A, Li Z, Fung HL, Young JE, Agarwal S, Antosiewicz-Bourget J, Canto I, Giorgetti A, Israel MA, Kiskinis E, et al.: Somatic coding mutations in human induced pluripotent stem cells. Nature 2011,471(7336):63–67. 10.1038/nature09805
Hussein SM, Batada NN, Vuoristo S, Ching RW, Autio R, Narva E, Ng S, Sourour M, Hamalainen R, Olsson C, et al.: Copy number variation and selection during reprogramming to pluripotency. Nature 2011,471(7336):58–62. 10.1038/nature09871
Kim K, Doi A, Wen B, Ng K, Zhao R, Cahan P, Kim J, Aryee MJ, Ji H, Ehrlich L, et al.: Epigenetic memory in induced pluripotent stem cells. Nature 2010,467(7313):285–290. 10.1038/nature09342
Ohi Y, Qin H, Hong C, Blouin L, Polo JM, Guo T, Qi Z, Downey SL, Manos PD, Rossi DJ, et al.: Incomplete DNA methylation underlies a transcriptional memory of somatic cells in human iPS cells. Nature Cell Biol 2011,13(5):541–549. 10.1038/ncb2239
Polo JM, Liu S, Figueroa ME, Kulalert W, Eminli S, Tan KY, Apostolou E, Stadtfeld M, Li Y, Shioda T, et al.: Cell type of origin influences the molecular and functional properties of mouse induced pluripotent stem cells. Nat Biotechnol 2010,28(8):848–855. 10.1038/nbt.1667
Zhao T, Zhang ZN, Rong Z, Xu Y: Immunogenicity of induced pluripotent stem cells. Nature 2011,474(7350):212–215.
Smith AG, Hooper ML: Buffalo rat liver cells produce a diffusible activity which inhibits the differentiation of murine embryonal carcinoma and embryonic stem cells. Developmental Biol 1987,121(1):1–9. 10.1016/0012-1606(87)90132-1
Smith AG, Heath JK, Donaldson DD, Wong GG, Moreau J, Stahl M, Rogers D: Inhibition of pluripotential embryonic stem cell differentiation by purified polypeptides. Nature 1988,336(6200):688–690. 10.1038/336688a0
Williams RL, Hilton DJ, Pease S, Willson TA, Stewart CL, Gearing DP, Wagner EF, Metcalf D, Nicola NA, Gough NM: Myeloid leukaemia inhibitory factor maintains the developmental potential of embryonic stem cells. Nature 1988,336(6200):684–687. 10.1038/336684a0
Stewart CL, Kaspar P, Brunet LJ, Bhatt H, Gadi I, Kontgen F, Abbondanzo SJ: Blastocyst implantation depends on maternal expression of leukaemia inhibitory factor. Nature 1992,359(6390):76–79. 10.1038/359076a0
Niwa H, Burdon T, Chambers I, Smith A: Self-renewal of pluripotent embryonic stem cells is mediated via activation of STAT3. Genes & development 1998,12(13):2048–2060. 10.1101/gad.12.13.2048
Yoshida K, Chambers I, Nichols J, Smith A, Saito M, Yasukawa K, Shoyab M, Taga T, Kishimoto T: Maintenance of the pluripotential phenotype of embryonic stem cells through direct activation of gp130 signalling pathways. Mechanisms of development 1994,45(2):163–171. 10.1016/0925-4773(94)90030-2
Nichols J, Chambers I, Taga T, Smith A: Physiological rationale for responsiveness of mouse embryonic stem cells to gp130 cytokines. Development 2001,128(12):2333–2339.
Ying QL, Nichols J, Chambers I, Smith A: BMP induction of Id proteins suppresses differentiation and sustains embryonic stem cell self-renewal in collaboration with STAT3. Cell 2003,115(3):281–292. 10.1016/S0092-8674(03)00847-X
Wilson PA, Hemmati-Brivanlou A: Induction of epidermis and inhibition of neural fate by Bmp-4. Nature 1995,376(6538):331–333. 10.1038/376331a0
Burdon T, Stracey C, Chambers I, Nichols J, Smith A: Suppression of SHP-2 and ERK signalling promotes self-renewal of mouse embryonic stem cells. Developmental biology 1999,210(1):30–43. 10.1006/dbio.1999.9265
Kunath T, Saba-El-Leil MK, Almousailleakh M, Wray J, Meloche S, Smith A: FGF stimulation of the Erk1/2 signalling cascade triggers transition of pluripotent embryonic stem cells from self-renewal to lineage commitment. Development 2007,134(16):2895–2902. 10.1242/dev.02880
Ying QL, Wray J, Nichols J, Batlle-Morera L, Doble B, Woodgett J, Cohen P, Smith A: The ground state of embryonic stem cell self-renewal. Nature 2008,453(7194):519–523. 10.1038/nature06968
Silva J, Barrandon O, Nichols J, Kawaguchi J, Theunissen TW, Smith A: Promotion of reprogramming to ground state pluripotency by signal inhibition. PLoS biology 2008,6(10):e253. 10.1371/journal.pbio.0060253
Nichols J, Silva J, Roode M, Smith A: Suppression of Erk signalling promotes ground state pluripotency in the mouse embryo. Development 2009,136(19):3215–3222. 10.1242/dev.038893
Buehr M, Meek S, Blair K, Yang J, Ure J, Silva J, McLay R, Hall J, Ying QL, Smith A: Capture of authentic embryonic stem cells from rat blastocysts. Cell 2008,135(7):1287–1298. 10.1016/j.cell.2008.12.007
Li P, Tong C, Mehrian-Shai R, Jia L, Wu N, Yan Y, Maxson RE, Schulze EN, Song H, Hsieh CL, et al.: Germline competent embryonic stem cells derived from rat blastocysts. Cell 2008,135(7):1299–1310. 10.1016/j.cell.2008.12.006
Nichols J, Jones K, Phillips JM, Newland SA, Roode M, Mansfield W, Smith A, Cooke A: Validated germline-competent embryonic stem cell lines from nonobese diabetic mice. Nature medicine 2009,15(7):814–818. 10.1038/nm.1996
Guo G, Yang J, Nichols J, Hall JS, Eyres I, Mansfield W, Smith A: Klf4 reverts developmentally programmed restriction of ground state pluripotency. Development 2009,136(7):1063–1069. 10.1242/dev.030957
Lyon MF: Gene action in the X-chromosome of the mouse (Mus musculus L.). Nature 1961, 190: 372–373. 10.1038/190372a0
Deuve JL, Avner P: The coupling of X-chromosome inactivation to pluripotency. Annual review of cell and developmental biology 2011, 27: 611–629. 10.1146/annurev-cellbio-092910-154020
Beard C, Li E, Jaenisch R: Loss of methylation activates Xist in somatic but not in embryonic cells. Genes & development 1995,9(19):2325–2334. 10.1101/gad.9.19.2325
Tai HH, Gordon J, McBurney MW: Xist is expressed in female embryonal carcinoma cells with two active X chromosomes. Somatic cell and molecular genetics 1994,20(3):171–182. 10.1007/BF02254758
Wang W, Yang J, Liu H, Lu D, Chen X, Zenonos Z, Campos LS, Rad R, Guo G, Zhang S, et al.: Rapid and efficient reprogramming of somatic cells to induced pluripotent stem cells by retinoic acid receptor gamma and liver receptor homolog 1. P Natl Acad Sci USA 2011,108(45):18283–18288. 10.1073/pnas.1100893108
Gardner RL: Mouse chimeras obtained by the injection of cells into the blastocyst. Nature 1968,220(5167):596–597. 10.1038/220596a0
Gardner RL, Rossant J: Investigation of the fate of 4–5 day post-coitum mouse inner cell mass cells by blastocyst injection. Journal of embryology and experimental morphology 1979, 52: 141–152.
Doetschman T, Williams P, Maeda N: Establishment of hamster blastocyst-derived embryonic stem (ES) cells. Developmental biology 1988,127(1):224–227. 10.1016/0012-1606(88)90204-7
Graves KH, Moreadith RW: Derivation and characterization of putative pluripotential embryonic stem cells from preimplantation rabbit embryos. Molecular reproduction and development 1993,36(4):424–433. 10.1002/mrd.1080360404
Notarianni E, Galli C, Laurie S, Moor RM, Evans MJ: Derivation of pluripotent, embryonic cell lines from the pig and sheep. Journal of reproduction and fertility 1991, 43: 255–260.
Notarianni E, Laurie S, Moor RM, Evans MJ: Maintenance and differentiation in culture of pluripotential embryonic cell lines from pig blastocysts. Journal of reproduction and fertility 1990, 41: 51–56.
Pain B, Clark ME, Shen M, Nakazawa H, Sakurai M, Samarut J, Etches RJ: Long-term in vitro culture and characterisation of avian embryonic stem cells with multiple morphogenetic potentialities. Development 1996,122(8):2339–2348.
Saito S, Strelchenko N, Niemann H: Bovine Embryonic Stem Cell-Like Cell-Lines Cultured over Several Passages. Roux Arch Dev Biol 1992,201(3):134–141. 10.1007/BF00188711
Stice SL, Strelchenko NS, Keefer CL, Matthews L: Pluripotent bovine embryonic cell lines direct embryonic development following nuclear transfer. Biology of reproduction 1996,54(1):100–110. 10.1095/biolreprod54.1.100
Sukoyan MA, Vatolin SY, Golubitsa AN, Zhelezova AI, Semenova LA, Serov OL: Embryonic stem cells derived from morulae, inner cell mass, and blastocysts of mink: comparisons of their pluripotencies. Molecular reproduction and development 1993,36(2):148–158. 10.1002/mrd.1080360205
Thomson JA, Kalishman J, Golos TG, Durning M, Harris CP, Becker RA, Hearn JP: Isolation of a primate embryonic stem cell line. Proceedings of the National Academy of Sciences of the United States of America 1995,92(17):7844–7848. 10.1073/pnas.92.17.7844
Thomson JA, Kalishman J, Golos TG, Durning M, Harris CP, Hearn JP: Pluripotent cell lines derived from common marmoset (Callithrix jacchus) blastocysts. Biology of reproduction 1996,55(2):254–259. 10.1095/biolreprod55.2.254
Thomson JA, Itskovitz-Eldor J, Shapiro SS, Waknitz MA, Swiergiel JJ, Marshall VS, Jones JM: Embryonic stem cell lines derived from human blastocysts. Science (New York, NY 1998,282(5391):1145–1147.
Daheron L, Opitz SL, Zaehres H, Lensch MW, Andrews PW, Itskovitz-Eldor J, Daley GQ: LIF/STAT3 signaling fails to maintain self-renewal of human embryonic stem cells. Stem cells (Dayton, Ohio) 2004,22(5):770–778. 10.1634/stemcells.22-5-770
Humphrey RK, Beattie GM, Lopez AD, Bucay N, King CC, Firpo MT, Rose-John S, Hayek A: Maintenance of pluripotency in human embryonic stem cells is STAT3 independent. Stem cells (Dayton, Ohio) 2004,22(4):522–530. 10.1634/stemcells.22-4-522
Gerami-Naini B, Dovzhenko OV, Durning M, Wegner FH, Thomson JA, Golos TG: Trophoblast differentiation in embryoid bodies derived from human embryonic stem cells. Endocrinology 2004,145(4):1517–1524.
Xu RH, Chen X, Li DS, Li R, Addicks GC, Glennon C, Zwaka TP, Thomson JA: BMP4 initiates human embryonic stem cell differentiation to trophoblast. Nat Biotechnol 2002,20(12):1261–1264. 10.1038/nbt761
Beattie GM, Lopez AD, Bucay N, Hinton A, Firpo MT, King CC, Hayek A: Activin A maintains pluripotency of human embryonic stem cells in the absence of feeder layers. Stem cells (Dayton, Ohio) 2005,23(4):489–495. 10.1634/stemcells.2004-0279
Vallier L, Alexander M, Pedersen RA: Activin/Nodal and FGF pathways cooperate to maintain pluripotency of human embryonic stem cells. J Cell Sci 2005,118(Pt 19):4495–4509.
Wang G, Zhang H, Zhao Y, Li J, Cai J, Wang P, Meng S, Feng J, Miao C, Ding M, et al.: Noggin and bFGF cooperate to maintain the pluripotency of human embryonic stem cells in the absence of feeder layers. Biochemical and biophysical research communications 2005,330(3):934–942. 10.1016/j.bbrc.2005.03.058
Xu C, Rosler E, Jiang J, Lebkowski JS, Gold JD, O'Sullivan C, Delavan-Boorsma K, Mok M, Bronstein A, Carpenter MK: Basic fibroblast growth factor supports undifferentiated human embryonic stem cell growth without conditioned medium. Stem cells (Dayton, Ohio) 2005,23(3):315–323. 10.1634/stemcells.2004-0211
Adewumi O, Aflatoonian B, Ahrlund-Richter L, Amit M, Andrews PW, Beighton G, Bello PA, Benvenisty N, Berry LS, Bevan S, et al.: Characterization of human embryonic stem cell lines by the International Stem Cell Initiative. Nat Biotechnol 2007,25(7):803–816. 10.1038/nbt1318
Kim JB, Greber B, Arauzo-Bravo MJ, Meyer J, Park KI, Zaehres H, Scholer HR: Direct reprogramming of human neural stem cells by OCT4. Nature 2009,461(7264):649–643. 10.1038/nature08436
Loh YH, Agarwal S, Park IH, Urbach A, Huo H, Heffner GC, Kim K, Miller JD, Ng K, Daley GQ: Generation of induced pluripotent stem cells from human blood. Blood 2009,113(22):5476–5479. 10.1182/blood-2009-02-204800
Kuijk EW, van Tol LT, Van de Velde H, Wubbolts R, Welling M, Geijsen N, Roelen BA: The roles of FGF and MAP kinase signaling in the segregation of the epiblast and hypoblast cell lineages in bovine and human embryos. Development 2012,139(5):871–882. 10.1242/dev.071688
Roode M, Blair K, Snell P, Elder K, Marchant S, Smith A, Nichols J: Human hypoblast formation is not dependent on FGF signalling. Developmental biology 2012,361(2):358–363. 10.1016/j.ydbio.2011.10.030
O'Leary T, Heindryckx B, Lierman S, van Bruggen D, Goeman JJ, Vandewoestyne M, Deforce D, de Sousa Lopes SM, De Sutter P: Tracking the progression of the human inner cell mass during embryonic stem cell derivation. Nat Biotechnol 2012,30(3):278–282. 10.1038/nbt.2135
Guo G, Smith A: A genome-wide screen in EpiSCs identifies Nr5a nuclear receptors as potent inducers of ground state pluripotency. Development 2010,137(19):3185–3192. 10.1242/dev.052753
Bao S, Tang F, Li X, Hayashi K, Gillich A, Lao K, Surani MA: Epigenetic reversion of post-implantation epiblast to pluripotent embryonic stem cells. Nature 2009,461(7268):1292–1295. 10.1038/nature08534
Hanna J, Cheng AW, Saha K, Kim J, Lengner CJ, Soldner F, Cassady JP, Muffat J, Carey BW, Jaenisch R: Human embryonic stem cells with biological and epigenetic characteristics similar to those of mouse ESCs. P NATL ACAD SCI USA 2010,107(20):9222–9227. 10.1073/pnas.1004584107
Buecker C, Chen HH, Polo JM, Daheron L, Bu L, Barakat TS, Okwieka P, Porter A, Gribnau J, Hochedlinger K, et al.: A murine ESC-like state facilitates transgenesis and homologous recombination in human pluripotent stem cells. Cell stem cell 2010,6(6):535–546. 10.1016/j.stem.2010.05.003
Li W, Wei W, Zhu S, Zhu J, Shi Y, Lin T, Hao E, Hayek A, Deng H, Ding S: Generation of rat and human induced pluripotent stem cells by combining genetic reprogramming and chemical inhibitors. Cell stem cell 2009,4(1):16–19. 10.1016/j.stem.2008.11.014
Tang F, Barbacioru C, Bao S, Lee C, Nordman E, Wang X, Lao K, Surani MA: Tracing the derivation of embryonic stem cells from the inner cell mass by single-cell RNA-Seq analysis. Cell stem cell 2010,6(5):468–478. 10.1016/j.stem.2010.03.015
Chou YF, Chen HH, Eijpe M, Yabuuchi A, Chenoweth JG, Tesar P, Lu J, McKay RD, Geijsen N: The growth factor environment defines distinct pluripotent ground states in novel blastocyst-derived stem cells. Cell 2008,135(3):449–461. 10.1016/j.cell.2008.08.035
Han DW, Tapia N, Hermann A, Hemmer K, Hoing S, Arauzo-Bravo MJ, Zaehres H, Wu G, Frank S, Moritz S, et al.: Direct reprogramming of fibroblasts into neural stem cells by defined factors. Cell stem cell 2012,10(4):465–472. 10.1016/j.stem.2012.02.021
Wright AJ, Andrews PW: Surface marker antigens in the characterization of human embryonic stem cells. Stem cell research 2009.
Amps K, Andrews PW, Anyfantis G, Armstrong L, Avery S, Baharvand H, Baker J, Baker D, Munoz MB, Beil S, et al.: Screening ethnically diverse human embryonic stem cells identifies a chromosome 20 minimal amplicon conferring growth advantage. Nat Biotechnol 2011,29(12):1132–1144. 10.1038/nbt.2051
Brimble SN, Zeng X, Weiler DA, Luo Y, Liu Y, Lyons IG, Freed WJ, Robins AJ, Rao MS, Schulz TC: Karyotypic stability, genotyping, differentiation, feeder-free maintenance, and gene expression sampling in three human embryonic stem cell lines derived prior to August 9, 2001. Stem cells and development 2004,13(6):585–597. 10.1089/scd.2004.13.585
Buzzard JJ, Gough NM, Crook JM, Colman A: Karyotype of human ES cells during extended culture. Nat Biotechnol 2004,22(4):381–382. author reply 382 10.1038/nbt0404-381
Lefort N, Feyeux M, Bas C, Feraud O, Bennaceur-Griscelli A, Tachdjian G, Peschanski M, Perrier AL: Human embryonic stem cells reveal recurrent genomic instability at 20q11.21. Nat Biotechnol 2008,26(12):1364–1366. 10.1038/nbt.1509
Mayshar Y, Ben-David U, Lavon N, Biancotti JC, Yakir B, Clark AT, Plath K, Lowry WE, Benvenisty N: Identification and classification of chromosomal aberrations in human induced pluripotent stem cells. Cell stem cell 2010,7(4):521–531. 10.1016/j.stem.2010.07.017
Spits C, Mateizel I, Geens M, Mertzanidou A, Staessen C, Vandeskelde Y, Van der Elst J, Liebaers I, Sermon K: Recurrent chromosomal abnormalities in human embryonic stem cells. Nat Biotechnol 2008,26(12):1361–1363. 10.1038/nbt.1510
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JO and PL wrote the manuscript. All authors read and approved the final manuscript.
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Ooi, J., Liu, P. Pluripotency and its layers of complexity. Cell Regen 1, 7 (2012). https://doi.org/10.1186/2045-9769-1-7
- Naïve pluripotency
- Primed pluripotency
- Embryonic stem cells
- Induced pluripotent stem cells
- Epiblast stem cells