{"title":"卵发生机制:秀丽隐杆线虫种系囊肿的教训","authors":"Kenji Kimura, Fumio Motegi","doi":"10.1016/j.semcdb.2025.103644","DOIUrl":null,"url":null,"abstract":"<div><div>Germ cells are organized into a syncytial architecture, wherein individual cells remain connected via intercellular bridges. Within this structural framework, known as germline cysts, a subset of germ cells enlarges and develops into oocytes, while others shrink and are eliminated through cell death. Recent studies with <em>Caenorhabditis elegans</em> have revealed that both apoptosis-mediated germ cell death and enlargement of surviving germ cells are regulated by mechanical forces. Germ cells exhibit stochastic fluctuations in volume driven by actomyosin contractility. This initial size heterogeneity is progressively amplified due to mechanical instability driven by differential hydrostatic pressure within the cyst, which biases smaller cells toward shrinkage and subsequent apoptotic death. This mechanical instability is further reinforced by the RAS/MAPK signaling cascade and the ECT-2/RhoA pathway, both of which enhance actomyosin contractility. Surviving germ cells continue to grow by acquiring the cytoplasmic materials through actomyosin contractility-mediated hydrodynamic flow within the cyst. Collectively, these findings highlight the critical role of mechanical forces in modulating cell fate decisions between survival and death, facilitating cell volume dynamics and maintaining germline homeostasis during oogenesis.</div></div>","PeriodicalId":21735,"journal":{"name":"Seminars in cell & developmental biology","volume":"175 ","pages":"Article 103644"},"PeriodicalIF":6.0000,"publicationDate":"2025-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Mechanics of oogenesis: Lessons from C. elegans germline cysts\",\"authors\":\"Kenji Kimura, Fumio Motegi\",\"doi\":\"10.1016/j.semcdb.2025.103644\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Germ cells are organized into a syncytial architecture, wherein individual cells remain connected via intercellular bridges. Within this structural framework, known as germline cysts, a subset of germ cells enlarges and develops into oocytes, while others shrink and are eliminated through cell death. Recent studies with <em>Caenorhabditis elegans</em> have revealed that both apoptosis-mediated germ cell death and enlargement of surviving germ cells are regulated by mechanical forces. Germ cells exhibit stochastic fluctuations in volume driven by actomyosin contractility. This initial size heterogeneity is progressively amplified due to mechanical instability driven by differential hydrostatic pressure within the cyst, which biases smaller cells toward shrinkage and subsequent apoptotic death. This mechanical instability is further reinforced by the RAS/MAPK signaling cascade and the ECT-2/RhoA pathway, both of which enhance actomyosin contractility. Surviving germ cells continue to grow by acquiring the cytoplasmic materials through actomyosin contractility-mediated hydrodynamic flow within the cyst. Collectively, these findings highlight the critical role of mechanical forces in modulating cell fate decisions between survival and death, facilitating cell volume dynamics and maintaining germline homeostasis during oogenesis.</div></div>\",\"PeriodicalId\":21735,\"journal\":{\"name\":\"Seminars in cell & developmental biology\",\"volume\":\"175 \",\"pages\":\"Article 103644\"},\"PeriodicalIF\":6.0000,\"publicationDate\":\"2025-08-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Seminars in cell & developmental biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1084952125000540\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Seminars in cell & developmental biology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1084952125000540","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
Mechanics of oogenesis: Lessons from C. elegans germline cysts
Germ cells are organized into a syncytial architecture, wherein individual cells remain connected via intercellular bridges. Within this structural framework, known as germline cysts, a subset of germ cells enlarges and develops into oocytes, while others shrink and are eliminated through cell death. Recent studies with Caenorhabditis elegans have revealed that both apoptosis-mediated germ cell death and enlargement of surviving germ cells are regulated by mechanical forces. Germ cells exhibit stochastic fluctuations in volume driven by actomyosin contractility. This initial size heterogeneity is progressively amplified due to mechanical instability driven by differential hydrostatic pressure within the cyst, which biases smaller cells toward shrinkage and subsequent apoptotic death. This mechanical instability is further reinforced by the RAS/MAPK signaling cascade and the ECT-2/RhoA pathway, both of which enhance actomyosin contractility. Surviving germ cells continue to grow by acquiring the cytoplasmic materials through actomyosin contractility-mediated hydrodynamic flow within the cyst. Collectively, these findings highlight the critical role of mechanical forces in modulating cell fate decisions between survival and death, facilitating cell volume dynamics and maintaining germline homeostasis during oogenesis.
期刊介绍:
Seminars in Cell and Developmental Biology is a review journal dedicated to keeping scientists informed of developments in the field of molecular cell and developmental biology, on a topic by topic basis. Each issue is thematic in approach, devoted to an important topic of interest to cell and developmental biologists, focusing on the latest advances and their specific implications.
The aim of each issue is to provide a coordinated, readable, and lively review of a selected area, published rapidly to ensure currency.