Germ Cell Differentiation in Culture

T. Noce
{"title":"Germ Cell Differentiation in Culture","authors":"T. Noce","doi":"10.1274/JMOR.20.69","DOIUrl":null,"url":null,"abstract":"The generation of animals cloned by means of the nuclear transfer technique indicates that somatic cell nuc le i can be rep rogrammed when t hey a re transplanted into the egg cytoplasm—in other words, the transplanted somatic nuclei can be induced to return to a pluripotent state similar to that of the nuclei of fert il ized eggs. Therefore, the potential for both reprogramming and pluripotency is retained in germ cells throughout their development. For example, embryonic germ (EG) cells that are generated from primordial germ cells (PGCs) show similar pluripotency to the undifferentiated embryonic stem (ES) cells that originate in the inner cell mass of blastocyst embryos in mice [1 ] . And some te ra tomas tha t genera te differentiated cells of various types—from all three pr imary germ layers—or ig inate in PGCs in the embryonic gonads [2]. Therefore, germ cells must have the ab i l i t y to be reprogrammed, as we l l as to differentiate to form gametes. So how do germ cells acquire these character ist ics, and how are they maintained during development? The discovery of the molecular and cellular mechanisms that are involved in these processes will provide important insights not only for basic research into reproductive biology but also for the development of new techniques for regenerative medical treatments. There is an urgent need to develop i n v i t r o s ys tems t ha t can mode l t he en t i r e developmental process—from pluripotent stem cells to func t i ona l spe rm and eggs—to f u r t he r ou r understanding of the mechanisms of germ-cel l differentiation.","PeriodicalId":90599,"journal":{"name":"Journal of mammalian ova research","volume":"32 1","pages":"69-73"},"PeriodicalIF":0.0000,"publicationDate":"2003-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of mammalian ova research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1274/JMOR.20.69","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract

The generation of animals cloned by means of the nuclear transfer technique indicates that somatic cell nuc le i can be rep rogrammed when t hey a re transplanted into the egg cytoplasm—in other words, the transplanted somatic nuclei can be induced to return to a pluripotent state similar to that of the nuclei of fert il ized eggs. Therefore, the potential for both reprogramming and pluripotency is retained in germ cells throughout their development. For example, embryonic germ (EG) cells that are generated from primordial germ cells (PGCs) show similar pluripotency to the undifferentiated embryonic stem (ES) cells that originate in the inner cell mass of blastocyst embryos in mice [1 ] . And some te ra tomas tha t genera te differentiated cells of various types—from all three pr imary germ layers—or ig inate in PGCs in the embryonic gonads [2]. Therefore, germ cells must have the ab i l i t y to be reprogrammed, as we l l as to differentiate to form gametes. So how do germ cells acquire these character ist ics, and how are they maintained during development? The discovery of the molecular and cellular mechanisms that are involved in these processes will provide important insights not only for basic research into reproductive biology but also for the development of new techniques for regenerative medical treatments. There is an urgent need to develop i n v i t r o s ys tems t ha t can mode l t he en t i r e developmental process—from pluripotent stem cells to func t i ona l spe rm and eggs—to f u r t he r ou r understanding of the mechanisms of germ-cel l differentiation.
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培养中的生殖细胞分化
通过核移植技术克隆的动物表明,当体细胞核被重新移植到卵细胞质中时,体细胞核可以被重新编程,换句话说,移植的体细胞核可以被诱导回到类似于受精卵核的多能状态。因此,生殖细胞在整个发育过程中都保留了重编程和多能性的潜力。例如,由原始生殖细胞(PGCs)产生的胚胎生殖细胞(EG)与起源于小鼠[1]囊胚内细胞群的未分化胚胎干(ES)细胞表现出类似的多能性。还有一些从所有三个初级胚层中产生不同类型分化细胞的肿瘤,或者在胚胎性腺中产生PGCs。因此,生殖细胞必须具有可重新编程的ab - i - 1,因为我们必须分化形成配子。那么,生殖细胞是如何获得这些特性的,又是如何在发育过程中维持这些特性的呢?这些过程中涉及的分子和细胞机制的发现不仅将为生殖生物学的基础研究提供重要见解,而且还将为再生医学治疗的新技术的发展提供重要见解。目前迫切需要开发一种能够模拟多种发育过程(从多能干细胞到功能干细胞,再到生殖细胞和卵子)的新技术,以帮助我们更好地理解生殖细胞分化的机制。
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