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{"title":"The stemness of neural crest cells and their derivatives","authors":"Takahiro Kunisada, Ken-Ichi Tezulka, Hitomi Aoki, Tsutomu Motohashi","doi":"10.1002/bdrc.21079","DOIUrl":null,"url":null,"abstract":"<p>Neural crest cells (NCCs) are unique to vertebrates and emerge from the border of the neural plate and subsequently migrate extensively throughout the embryo after which they differentiate into many types of cells. This multipotency is the main reason why NCCs are regarded as a versatile tool for stem cell biology and have been gathering attention for their potential use in stem cell based therapy. Multiple sets of networks comprised of signaling molecules and transcription factors regulate every developmental phase of NCCs, including maintenance of their multipotency. Pluripotent stem cell lines, such as embryonic stem cells and induced pluripotent stem (iPS) cells, facilitate the induction of NCCs in combination with sophisticated culture systems used for neural stem cells, although at present, clinical experiments for NCC-based cell therapy need to be improved. Unexpectedly, the multipotency of NCCs is maintained after they reach the target tissues as tissue neural crest stem cells (NCSCs) that may contribute to the establishment of NCC-derived multipotential stem cells. In addition, under specific culture conditions, fate-restricted unipotent descendants of NCCs, such as melanoblasts, show multipotency to differentiate into melanocytes, neurons, and glia cells. These properties contribute to the additional versatility of NCCs for therapeutic application and to better understand NCC development. Birth Defects Research (Part C) 102:251–262, 2014. © 2014 Wiley Periodicals, Inc.</p>","PeriodicalId":55352,"journal":{"name":"Birth Defects Research Part C-Embryo Today-Reviews","volume":"102 3","pages":"251-262"},"PeriodicalIF":0.0000,"publicationDate":"2014-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/bdrc.21079","citationCount":"22","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Birth Defects Research Part C-Embryo Today-Reviews","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/bdrc.21079","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 22
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Abstract
Neural crest cells (NCCs) are unique to vertebrates and emerge from the border of the neural plate and subsequently migrate extensively throughout the embryo after which they differentiate into many types of cells. This multipotency is the main reason why NCCs are regarded as a versatile tool for stem cell biology and have been gathering attention for their potential use in stem cell based therapy. Multiple sets of networks comprised of signaling molecules and transcription factors regulate every developmental phase of NCCs, including maintenance of their multipotency. Pluripotent stem cell lines, such as embryonic stem cells and induced pluripotent stem (iPS) cells, facilitate the induction of NCCs in combination with sophisticated culture systems used for neural stem cells, although at present, clinical experiments for NCC-based cell therapy need to be improved. Unexpectedly, the multipotency of NCCs is maintained after they reach the target tissues as tissue neural crest stem cells (NCSCs) that may contribute to the establishment of NCC-derived multipotential stem cells. In addition, under specific culture conditions, fate-restricted unipotent descendants of NCCs, such as melanoblasts, show multipotency to differentiate into melanocytes, neurons, and glia cells. These properties contribute to the additional versatility of NCCs for therapeutic application and to better understand NCC development. Birth Defects Research (Part C) 102:251–262, 2014. © 2014 Wiley Periodicals, Inc.
神经嵴细胞及其衍生物的干性
神经嵴细胞(Neural crest cells, NCCs)是脊椎动物特有的细胞,起源于神经板的边缘,随后在胚胎中广泛迁移,并分化成多种类型的细胞。这种多能性是NCCs被视为干细胞生物学的多功能工具的主要原因,并因其在干细胞治疗中的潜在用途而受到关注。由信号分子和转录因子组成的多组网络调节着NCCs的每个发育阶段,包括维持其多能性。多能干细胞系,如胚胎干细胞和诱导多能干细胞(iPS)细胞,与用于神经干细胞的复杂培养系统相结合,有助于诱导ncc,尽管目前,基于ncc的细胞治疗的临床实验需要改进。出乎意料的是,ncc作为组织神经嵴干细胞(tissue neural crest stem cells, NCSCs)到达靶组织后仍能保持多能性,这可能有助于ncc衍生的多能性干细胞的建立。此外,在特定的培养条件下,ncc的命运受限的单能后代,如黑素母细胞,表现出多能分化为黑素细胞、神经元和胶质细胞。这些特性有助于NCC在治疗应用中的多功能性,并有助于更好地了解NCC的发展。出生缺陷研究(C辑)(2):251 - 262,2014。©2014 Wiley期刊公司
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