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the other hand, several marked differences can be observed between the pre- and post-implantation epiblasts, such as their difference in morphology, in which the epiblast after implantation changes its morphology into a cup-like shape called the "egg cylinder" as well as chromosomal alteration in which one of the X-chromosomes under random inactivation in the early stage of the egg cylinder, known as
443:, and, despite advances, were never approved for clinical stage research in the United States until recently. Currently, autologous iPSC-derived dopaminergic progenitor cells are used in trials for treating Parkinson's disease. Setbacks such as low replication rates and early senescence have also been encountered when making iPSCs, hindering their use as ESCs replacements. 685:. Examples of oligopotent stem cells are the lymphoid or myeloid stem cells. A lymphoid cell specifically, can give rise to various blood cells such as B and T cells, however, not to a different blood cell type like a red blood cell. Examples of progenitor cells are vascular stem cells that have the capacity to become both 364:. These transcription factors play a key role in determining the state of these cells and also highlights the fact that these somatic cells do preserve the same genetic information as early embryonic cells. The ability to induce cells into a pluripotent state was initially pioneered in 2006 using mouse 498:
The baseline stem cells commonly used in science that are referred as embryonic stem cells (ESCs) are derived from a pre-implantation epiblast; such epiblast is able to generate the entire fetus, and one epiblast cell is able to contribute to all cell lineages if injected into another blastocyst. On
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factors are also thought to be involved in the actual reprogramming of somatic cells in order to induce pluripotency. It has been theorized that certain epigenetic factors might actually work to clear the original somatic epigenetic marks in order to acquire the new epigenetic marks that are part of
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the Nobel Prize in Physiology or Medicine. This was then followed in 2007 by the successful induction of human iPSCs derived from human dermal fibroblasts using methods similar to those used for the induction of mouse cells. These induced cells exhibit similar traits to those of embryonic stem cells
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before and after implantation have produced proposals for classifying pluripotency into two states: "naive" and "primed", representing pre- and post-implantation epiblast, respectively. Naive-to-primed continuum is controlled by reduction of Sox2/Oct4 dimerization on SoxOct DNA elements controlling
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Research related to multipotent cells suggests that multipotent cells may be capable of conversion into unrelated cell types. In another case, human umbilical cord blood stem cells were converted into human neurons. There is also research on converting multipotent cells into pluripotent cells.
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Due to their great similarity to ESCs, the medical and research communities are interested iPSCs. iPSCs could potentially have the same therapeutic implications and applications as ESCs but without the controversial use of embryos in the process, a topic of great bioethical debate. The induced
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A fully differentiated cell can return to a state of totipotency. The conversion to totipotency is complex and not fully understood. In 2011, research revealed that cells may differentiate not into a fully totipotent cell, but instead into a "complex cellular variation" of totipotency.
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Some of the possible medical and therapeutic uses for iPSCs derived from patients include their use in cell and tissue transplants without the risk of rejection that is commonly encountered. iPSCs can potentially replace animal models unsuitable as well as
522:, which were first derived in laboratory in 2007. Both ESCs and EpiSCs are derived from epiblasts but at difference phases of development. Pluripotency is still intact in the post-implantation epiblast, as demonstrated by the conserved expression of 1079:
Asch R, Simerly C, Ord T, Ord VA, Schatten G (July 1995). "The stages at which human fertilization arrests: microtubule and chromosome configurations in inseminated oocytes which failed to complete fertilization and development in humans".
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naive pluripotency. Primed pluripotent stem cells from different species could be reset to naive state using a cocktail containing Klf4 and Sox2 or "super-Sox" − a chimeric transcription factor with enhanced capacity to dimerize with Oct4.
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MacCarthy, Caitlin M.; Wu, Guangming; Malik, Vikas; Menuchin-Lasowski, Yotam; Velychko, Taras; Keshet, Gal; Fan, Rui; Bedzhov, Ivan; Church, George M.; Jauch, Ralf; Cojocaru, Vlad; Schöler, Hans R.; Velychko, Sergiy (December 2023).
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Hematopoietic stem cells are an example of multipotency. When they differentiate into myeloid or lymphoid progenitor cells, they lose potency and become oligopotent cells with the ability to give rise to all cells of its
707:, a unipotent cell is the concept that one stem cell has the capacity to differentiate into only one cell type. It is currently unclear if true unipotent stem cells exist. Hepatoblasts, which differentiate into 41:
into other cell types. The more cell types a cell can differentiate into, the greater its potency. Potency is also described as the gene activation potential within a cell, which like a continuum, begins with
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have the gene activation potential to differentiate into discrete cell types. For example, a hematopoietic stem cell – and this cell type can differentiate itself into several types of blood cell like
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MSCs may prove to be a valuable source for stem cells from molars at 8–10 years of age, before adult dental calcification. MSCs can differentiate into osteoblasts, chondrocytes, and adipocytes.
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Takahashi K, Tanabe K, Ohnuki M, Narita M, Ichisaka T, Tomoda K, Yamanaka S (November 2007). "Induction of pluripotent stem cells from adult human fibroblasts by defined factors".
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signaling, and other inductive factors via the surrounding yolk sac and the trophoblast tissue, such that they become instructively specific according to the spatial organization.
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Brons IG, Smithers LE, Trotter MW, Rugg-Gunn P, Sun B, Chuva de Sousa Lopes SM, et al. (July 2007). "Derivation of pluripotent epiblast stem cells from mammalian embryos".
454:); researchers identified three neural-lineage-specific transcription factors that could directly convert mouse fibroblasts (connective tissue cells) into fully functional 2340:
Tallone T, Realini C, Böhmler A, Kornfeld C, Vassalli G, Moccetti T, et al. (April 2011). "Adult human adipose tissue contains several types of multipotent cells".
191:. Approximately four days after fertilization and after several cycles of cell division, these totipotent cells begin to specialize. The inner cell mass, the source of 2524:
Betts, J Gordon; Desaix, Peter; Johnson, Eddie; Johnson, Jody E; Korol, Oksana; Kruse, Dean; Poe, Brandon; Wise, James; Womble, Mark D; Young, Kelly A (June 8, 2023).
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achieving a pluripotent state. Chromatin is also reorganized in iPSCs and becomes like that found in ESCs in that it is less condensed and therefore more accessible.
155:. In the first hours after fertilization, this zygote divides into identical totipotent cells, which can later develop into any of the three germ layers of a human ( 2551: 995:
Sugimoto K, Gordon SP, Meyerowitz EM (April 2011). "Regeneration in plants and animals: dedifferentiation, transdifferentiation, or just differentiation?".
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tissue culture, especially by Kareem et al 2015, Kim et al 2018, and Rosspopoff et al 2017. This pluripotency is regulated by various regulators, including
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Guan K, Nayernia K, Maier LS, Wagner S, Dressel R, Lee JH, et al. (April 2006). "Pluripotency of spermatogonial stem cells from adult mouse testis".
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Takahashi K, Yamanaka S (August 2006). "Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors".
565: 518:, which distinguishes them from other known pluripotent stem cells. Cell lines derived from such post-implantation epiblasts are referred to as 2783: 1950:
Lawson KA, Meneses JJ, Pedersen RA (November 1991). "Clonal analysis of epiblast fate during germ layer formation in the mouse embryo".
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Ciosk R, DePalma M, Priess JR (February 2006). "Translational regulators maintain totipotency in the Caenorhabditis elegans germline".
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are examples of totipotent cells. In the spectrum of cell potency, totipotency represents the cell with the greatest
397:(ESCs) but do not require the use of embryos. Some of the similarities between ESCs and iPSCs include pluripotency, 261: 257: 828:
Schöler HR (2007). "The Potential of Stem Cells: An Inventory". In Knoepffler M, Schipanski D, Sorgner SL (eds.).
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Zhao Y, Mazzone T (December 2010). "Human cord blood stem cells and the journey to a cure for type 1 diabetes".
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The human development model can be used to describe how totipotent cells arise. Human development begins when a
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Another major difference is that post-implantation epiblast stem cells are unable to contribute to blastocyst
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Park IH, Lerou PH, Zhao R, Huo H, Daley GQ (2008). "Generation of human-induced pluripotent stem cells".
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Multipotent cells are found in many, but not all human cell types. Multipotent cells have been found in
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may play a role in maintaining totipotency at different stages of development in some species. Work with
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Induced pluripotent stem cells, commonly abbreviated as iPS cells or iPSCs, are a type of pluripotent
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Uccelli A, Moretta L, Pistoia V (September 2008). "Mesenchymal stem cells in health and disease".
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Beltrami AP, Barlucchi L, Torella D, Baker M, Limana F, Chimenti S, et al. (September 2003).
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Blog on treatment therapy using pluripotent stem cells and pluripotent stem cell derived exosomes
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Cell totipotency was discovered by Habertland and the term was coined by Thomas Hund Morgan.
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Osorno R, Tsakiridis A, Wong F, Cambray N, Economou C, Wilkie R, et al. (July 2012).
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Hackett JA, Sengupta R, Zylicz JJ, Murakami K, Lee C, Down TA, Surani MA (January 2013).
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For substances having the capacity to produce several distinct biological responses, see
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Ikeuchi M, Favero DS, Sakamoto Y, Iwase A, Coleman D, Rymen B, Sugimoto K (April 2019).
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In biology, oligopotency is the ability of progenitor cells to differentiate into a few
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fertilizes an egg and the resulting fertilized egg creates a single totipotent cell, a
2401: 2384: 2095:"The developmental dismantling of pluripotency is reversed by ectopic Oct4 expression" 1919: 1902: 860:. Advances in Biochemical Engineering/Biotechnology. Vol. 114. pp. 185–199. 2763: 2531: 2476: 2441: 2406: 2357: 2322: 2279: 2236: 2169: 2124: 2067: 2016: 1967: 1924: 1883: 1815: 1766: 1731: 1651: 1602: 1542: 1476: 1431: 1348: 1303: 1246: 1189: 1140: 1097: 1053: 1012: 977: 920: 897: 877: 833: 807: 682: 241: 2418: 2369: 2181: 2028: 1979: 1936: 1778: 1692:
Vierbuchen T, Ostermeier A, Pang ZP, Kokubu Y, Südhof TC, Wernig M (February 2010).
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Schweitzer JS, Song B, Herrington TM, Park TY, Lee N, Ko S, et al. (May 2020).
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Naive human pluripotent stem cell colony here seen growing on feeder cells (mouse).
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cell. In contrast, pluripotent cells can only differentiate into embryonic cells.
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Giorgetti A, Marchetto MC, Li M, Yu D, Fazzina R, Mu Y, et al. (July 2012).
1839:"Highly cooperative chimeric super-SOX induces naive pluripotency across species" 616: 462:
and the integrity of lineage commitment; and implies that with the proper tools,
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methylation (5mC) in primordial germ cells via the initial conversion of 5mC to
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Proceedings of the National Academy of Sciences of the United States of America
2011: 1994: 1851: 1838: 1810: 1793: 1528: 1462: 1385: 1048: 1031: 746: 725: 716: 698: 500: 256:(5hmC), a reaction driven by high levels of the ten-eleven dioxygenase enzymes 113: 34: 2385:"Adult cardiac stem cells are multipotent and support myocardial regeneration" 2353: 1879: 1008: 2823: 2517: 1622:"Personalized iPSC-Derived Dopamine Progenitor Cells for Parkinson's Disease" 535: 385: 314:'ability for many ') refers to a stem cell that has the potential to 285: 2221: 1289: 1232: 1207:
Hajkova P, Jeffries SJ, Lee C, Miller N, Jackson SP, Surani MA (July 2010).
1136: 2480: 2445: 2410: 2361: 2326: 2283: 2240: 2197:"Cord blood-derived neuronal cells by ectopic expression of Sox2 and c-Myc" 2173: 2128: 2071: 2020: 1887: 1819: 1770: 1735: 1694:"Direct conversion of fibroblasts to functional neurons by defined factors" 1655: 1606: 1546: 1480: 1435: 1307: 1250: 1193: 1144: 1057: 1016: 981: 901: 811: 792: 776:"Stem Cells Applications in Regenerative Medicine and Disease Therapeutics" 704: 353: 148: 55: 51: 47: 1971: 1963: 1928: 1762: 1637: 1101: 972: 955: 941:"What is the difference between totipotent, pluripotent, and multipotent?" 708: 686: 663: 655: 636: 628: 620: 440: 417: 416:
modifications are also common which is also consistent with the state of
413: 393: 319: 188: 69: 43: 2275: 2063: 1717: 1588: 1417: 1184: 1167: 856:, Wolf D (2009). "Totipotency, pluripotency and nuclear reprogramming". 2110: 1471: 873: 719:(epithelial cells of the bile duct), are bipotent. A close synonym for 678: 651: 640: 585: 581: 577: 573: 569: 408: 365: 237: 229: 180: 89: 77: 59: 1831: 1829: 1537: 2618: 1866:
Heard E (June 2004). "Recent advances in X-chromosome inactivation".
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artificially derived from a non-pluripotent cell, typically an adult
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differentiate into cells that will eventually become either the
2680: 2670: 1342: 455: 290: 236:-wide reprogramming leading to totipotency involves erasure of 233: 176: 175:). After reaching a 16-cell stage, the totipotent cells of the 152: 133: 125: 85: 1691: 2675: 2587: 2382: 2339: 2041: 1402:"Induced pluripotency: history, mechanisms, and applications" 1263: 712: 589: 539: 531: 477: 296: 213: 121: 46:
to designate a cell with the most differentiation potential,
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to divide and produce all of the differentiated cells in an
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Binder MD, Hirokawa N, Nobutaka, Windhorst U, eds. (2009).
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stem cells (cell colonies that are not yet differentiated).
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and can be reversed midway through induced expression of
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Ability of a cell to differentiate into other cell types
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cells are totipotent and may form all kinds of tissue.
112:'ability for all ') is the ability of a single 2504:"Cytokines & Cells Online Pathfinder Encyclopedia" 2194: 450:
can directly induce other defined somatic cell fates (
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Ohgushi H, Arima N, Taketani T (December 2011). "".
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enzymatic pathway. This pathway entails erasure of
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Nihon Rinsho. Japanese Journal of Clinical Medicine
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Biology-Online.org 793:10.1155/2016/6940283 555:Ranunculus asiaticus 452:transdifferentiation 437:embryonic stem cells 338:Induced pluripotency 246:base excision repair 228:In mouse primordial 218:RNA-binding proteins 193:embryonic stem cells 101:Totipotency (Latin: 2693:Embryonic stem cell 2502:Ibelgaufts, Horst. 2276:10.1038/nature04697 2268:2006Natur.440.1199G 2262:(7088): 1199–1203. 2213:2012PNAS..10912556G 2207:(31): 12556–12561. 2064:10.1038/nature05950 2056:2007Natur.448..191B 1718:10.1038/nature08797 1710:2010Natur.463.1035V 1704:(7284): 1035–1041. 1589:10.1038/cr.2012.175 1418:10.1101/gad.1963910 1282:2013Sci...339..448H 1225:2010Sci...329...78H 1185:10.4161/cc.7.7.5644 1129:2006Sci...311..851C 866:2009esc..book..185M 173:syncytiotrophoblast 2111:10.1242/dev.078071 1082:Human Reproduction 954:Western P (2009). 874:10.1007/10_2008_45 755:Induced stem cells 613: 562: 483: 301: 244:involving the DNA 94: 2817: 2816: 2764:Stem cell therapy 2643:Cancer stem cells 2537:978-1-947172-04-3 2440:(12): 2121–2127. 2105:(13): 2288–2298. 2050:(7150): 191–195. 1632:(20): 1926–1932. 1412:(20): 2239–2263. 1276:(6118): 448–452. 1123:(5762): 851–853. 915:Lodish H (2016). 883:978-3-540-88805-5 839:978-0-7546-5755-2 774:Mahla RS (2016). 534:in EpiSCs, until 433:controversial use 313: 242:DNA demethylation 111: 16:(Redirected from 2847: 2805: 2804: 2752:Related articles 2729:Neural stem cell 2638:Adult stem cells 2612: 2605: 2598: 2589: 2588: 2571: 2570: 2568: 2567: 2558:. 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Index

Totipotent
cell
differentiate
totipotency
pluripotency
multipotency
oligopotency
unipotency

Pluripotent
stem cells
blastocyst
placenta
morula
totipotent
cell
organism
Spores
zygotes
differentiation
embryonic
extraembryonic tissue
sperm
zygote
endoderm
mesoderm
ectoderm
cytotrophoblast
syncytiotrophoblast
morula

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