Generation of human oogonia from induced pluripotent stem cells in vitro

Human in vitro gametogenesis may transform reproductive medicine. Human pluripotent stem cells (hPSCs) have been induced into primordial germ cell-like cells (hPGCLCs); however, further differentiation to a mature germ cell has not been achieved. Here, we show that hPGCLCs differentiate progressivel...

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Vydáno v:Science (American Association for the Advancement of Science) Ročník 362; číslo 6412; s. 356
Hlavní autoři: Yamashiro, Chika, Sasaki, Kotaro, Yabuta, Yukihiro, Kojima, Yoji, Nakamura, Tomonori, Okamoto, Ikuhiro, Yokobayashi, Shihori, Murase, Yusuke, Ishikura, Yukiko, Shirane, Kenjiro, Sasaki, Hiroyuki, Yamamoto, Takuya, Saitou, Mitinori
Médium: Journal Article
Jazyk:angličtina
Vydáno: United States 19.10.2018
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ISSN:1095-9203, 1095-9203
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Abstract Human in vitro gametogenesis may transform reproductive medicine. Human pluripotent stem cells (hPSCs) have been induced into primordial germ cell-like cells (hPGCLCs); however, further differentiation to a mature germ cell has not been achieved. Here, we show that hPGCLCs differentiate progressively into oogonia-like cells during a long-term in vitro culture (approximately 4 months) in xenogeneic reconstituted ovaries with mouse embryonic ovarian somatic cells. The hPGCLC-derived oogonia display hallmarks of epigenetic reprogramming-genome-wide DNA demethylation, imprint erasure, and extinguishment of aberrant DNA methylation in hPSCs-and acquire an immediate precursory state for meiotic recombination. Furthermore, the inactive X chromosome shows a progressive demethylation and reactivation, albeit partially. These findings establish the germline competence of hPSCs and provide a critical step toward human in vitro gametogenesis.
AbstractList Human in vitro gametogenesis may transform reproductive medicine. Human pluripotent stem cells (hPSCs) have been induced into primordial germ cell-like cells (hPGCLCs); however, further differentiation to a mature germ cell has not been achieved. Here, we show that hPGCLCs differentiate progressively into oogonia-like cells during a long-term in vitro culture (approximately 4 months) in xenogeneic reconstituted ovaries with mouse embryonic ovarian somatic cells. The hPGCLC-derived oogonia display hallmarks of epigenetic reprogramming-genome-wide DNA demethylation, imprint erasure, and extinguishment of aberrant DNA methylation in hPSCs-and acquire an immediate precursory state for meiotic recombination. Furthermore, the inactive X chromosome shows a progressive demethylation and reactivation, albeit partially. These findings establish the germline competence of hPSCs and provide a critical step toward human in vitro gametogenesis.Human in vitro gametogenesis may transform reproductive medicine. Human pluripotent stem cells (hPSCs) have been induced into primordial germ cell-like cells (hPGCLCs); however, further differentiation to a mature germ cell has not been achieved. Here, we show that hPGCLCs differentiate progressively into oogonia-like cells during a long-term in vitro culture (approximately 4 months) in xenogeneic reconstituted ovaries with mouse embryonic ovarian somatic cells. The hPGCLC-derived oogonia display hallmarks of epigenetic reprogramming-genome-wide DNA demethylation, imprint erasure, and extinguishment of aberrant DNA methylation in hPSCs-and acquire an immediate precursory state for meiotic recombination. Furthermore, the inactive X chromosome shows a progressive demethylation and reactivation, albeit partially. These findings establish the germline competence of hPSCs and provide a critical step toward human in vitro gametogenesis.
Human in vitro gametogenesis may transform reproductive medicine. Human pluripotent stem cells (hPSCs) have been induced into primordial germ cell-like cells (hPGCLCs); however, further differentiation to a mature germ cell has not been achieved. Here, we show that hPGCLCs differentiate progressively into oogonia-like cells during a long-term in vitro culture (approximately 4 months) in xenogeneic reconstituted ovaries with mouse embryonic ovarian somatic cells. The hPGCLC-derived oogonia display hallmarks of epigenetic reprogramming-genome-wide DNA demethylation, imprint erasure, and extinguishment of aberrant DNA methylation in hPSCs-and acquire an immediate precursory state for meiotic recombination. Furthermore, the inactive X chromosome shows a progressive demethylation and reactivation, albeit partially. These findings establish the germline competence of hPSCs and provide a critical step toward human in vitro gametogenesis.
Author Shirane, Kenjiro
Yamamoto, Takuya
Yokobayashi, Shihori
Okamoto, Ikuhiro
Saitou, Mitinori
Murase, Yusuke
Kojima, Yoji
Ishikura, Yukiko
Sasaki, Kotaro
Yabuta, Yukihiro
Sasaki, Hiroyuki
Nakamura, Tomonori
Yamashiro, Chika
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References 30337398 - Science. 2018 Oct 19;362(6412):291-292
References_xml – reference: 30337398 - Science. 2018 Oct 19;362(6412):291-292
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Snippet Human in vitro gametogenesis may transform reproductive medicine. Human pluripotent stem cells (hPSCs) have been induced into primordial germ cell-like cells...
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StartPage 356
SubjectTerms Cellular Reprogramming Techniques - methods
DNA Methylation
Epigenesis, Genetic
Female
Humans
Induced Pluripotent Stem Cells - cytology
Oogenesis
Oogonia - cytology
Ovary - growth & development
Title Generation of human oogonia from induced pluripotent stem cells in vitro
URI https://www.ncbi.nlm.nih.gov/pubmed/30237246
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