原始生殖细胞的机械之旅

IF 5 2区 生物学 Q2 CELL BIOLOGY
Malhar Chitnis, Xu Gao, Jennifer Marlena, Andrew Holle
{"title":"原始生殖细胞的机械之旅","authors":"Malhar Chitnis, Xu Gao, Jennifer Marlena, Andrew Holle","doi":"10.1152/ajpcell.00404.2024","DOIUrl":null,"url":null,"abstract":"<p><p>Primordial germ cells (PGCs) are the earliest progenitors of germline cells of the gonads in animals. The tissues that arise from primordial germ cells give rise to the male as well as female gametes and are thus responsible for transmitting genetic information to subsequent generations. Their development from single cells to fully formed tissues has thus been of great importance. In most higher animals, PGCs are initially specified at a site away from the gonads. They then migrate across multiple tissue contexts to reach a mesodermal mass of cells called the genital ridge, where they associate with somatic cells to form the sex-specific reproductive organs. This migratory behavior has been studied extensively to identify the various tissues PGCs interact with and how this might affect their development. A crucial point overlooked by classical studies has been the physical environment experienced by PGCs as they migrate and the mechanical challenges they might encounter. It has long been understood that migrating cells can sense and adapt to physical forces around them via a variety of mechanisms. Studies have also shown that these mechanical signals can guide stem cell fate. In this review, we summarize the mechanical microenvironment of migrating PGCs in different organisms. We describe how cells can adapt to this environment and how this adaptation can influence cell fate. We propose that mechanical signals play a crucial role in normal development of the germline and shed light on this unexplored area of developmental biology.</p>","PeriodicalId":7585,"journal":{"name":"American journal of physiology. Cell physiology","volume":" ","pages":""},"PeriodicalIF":5.0000,"publicationDate":"2024-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The mechanical journey of primordial germ cells.\",\"authors\":\"Malhar Chitnis, Xu Gao, Jennifer Marlena, Andrew Holle\",\"doi\":\"10.1152/ajpcell.00404.2024\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Primordial germ cells (PGCs) are the earliest progenitors of germline cells of the gonads in animals. The tissues that arise from primordial germ cells give rise to the male as well as female gametes and are thus responsible for transmitting genetic information to subsequent generations. Their development from single cells to fully formed tissues has thus been of great importance. In most higher animals, PGCs are initially specified at a site away from the gonads. They then migrate across multiple tissue contexts to reach a mesodermal mass of cells called the genital ridge, where they associate with somatic cells to form the sex-specific reproductive organs. This migratory behavior has been studied extensively to identify the various tissues PGCs interact with and how this might affect their development. A crucial point overlooked by classical studies has been the physical environment experienced by PGCs as they migrate and the mechanical challenges they might encounter. It has long been understood that migrating cells can sense and adapt to physical forces around them via a variety of mechanisms. Studies have also shown that these mechanical signals can guide stem cell fate. In this review, we summarize the mechanical microenvironment of migrating PGCs in different organisms. We describe how cells can adapt to this environment and how this adaptation can influence cell fate. We propose that mechanical signals play a crucial role in normal development of the germline and shed light on this unexplored area of developmental biology.</p>\",\"PeriodicalId\":7585,\"journal\":{\"name\":\"American journal of physiology. Cell physiology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":5.0000,\"publicationDate\":\"2024-10-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"American journal of physiology. Cell physiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1152/ajpcell.00404.2024\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"American journal of physiology. Cell physiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1152/ajpcell.00404.2024","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

原始生殖细胞(PGC)是动物性腺生殖细胞的最早祖细胞。原始生殖细胞产生的组织可产生雄性配子和雌性配子,因此负责向后代传递遗传信息。因此,原始生殖细胞从单细胞发展为完全形成的组织具有重要意义。在大多数高等动物中,PGC 最初是在远离性腺的部位形成的。然后,它们穿过多个组织环境迁移到称为生殖脊的中胚层细胞群,在那里与体细胞结合形成性别特异的生殖器官。人们对这种迁移行为进行了广泛的研究,以确定 PGCs 与哪些组织发生相互作用,以及这种相互作用会如何影响它们的发育。经典研究忽略的一个关键点是 PGCs 迁徙时所经历的物理环境以及它们可能遇到的机械挑战。人们早就知道,迁移细胞可以通过各种机制感知并适应周围的物理力。研究还表明,这些机械信号可引导干细胞的命运。在这篇综述中,我们总结了不同生物体内迁移PGC的机械微环境。我们描述了细胞如何适应这种环境,以及这种适应如何影响细胞命运。我们提出,机械信号在生殖细胞的正常发育中起着至关重要的作用,并阐明了发育生物学中这一尚未探索的领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The mechanical journey of primordial germ cells.

Primordial germ cells (PGCs) are the earliest progenitors of germline cells of the gonads in animals. The tissues that arise from primordial germ cells give rise to the male as well as female gametes and are thus responsible for transmitting genetic information to subsequent generations. Their development from single cells to fully formed tissues has thus been of great importance. In most higher animals, PGCs are initially specified at a site away from the gonads. They then migrate across multiple tissue contexts to reach a mesodermal mass of cells called the genital ridge, where they associate with somatic cells to form the sex-specific reproductive organs. This migratory behavior has been studied extensively to identify the various tissues PGCs interact with and how this might affect their development. A crucial point overlooked by classical studies has been the physical environment experienced by PGCs as they migrate and the mechanical challenges they might encounter. It has long been understood that migrating cells can sense and adapt to physical forces around them via a variety of mechanisms. Studies have also shown that these mechanical signals can guide stem cell fate. In this review, we summarize the mechanical microenvironment of migrating PGCs in different organisms. We describe how cells can adapt to this environment and how this adaptation can influence cell fate. We propose that mechanical signals play a crucial role in normal development of the germline and shed light on this unexplored area of developmental biology.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
9.10
自引率
1.80%
发文量
252
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Cell Physiology is dedicated to innovative approaches to the study of cell and molecular physiology. Contributions that use cellular and molecular approaches to shed light on mechanisms of physiological control at higher levels of organization also appear regularly. Manuscripts dealing with the structure and function of cell membranes, contractile systems, cellular organelles, and membrane channels, transporters, and pumps are encouraged. Studies dealing with integrated regulation of cellular function, including mechanisms of signal transduction, development, gene expression, cell-to-cell interactions, and the cell physiology of pathophysiological states, are also eagerly sought. Interdisciplinary studies that apply the approaches of biochemistry, biophysics, molecular biology, morphology, and immunology to the determination of new principles in cell physiology are especially welcome.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信