Flora Llense, Teresa Ferraro, Xinyi Yang, Hanla Song, Michel Labouesse
{"title":"具有肌Deg/Enac通道的肌内蛋白和肠内蛋白促进肌肉协调和胚胎伸长。","authors":"Flora Llense, Teresa Ferraro, Xinyi Yang, Hanla Song, Michel Labouesse","doi":"10.1242/dev.204242","DOIUrl":null,"url":null,"abstract":"<p><p>Body axis elongation represents a fundamental morphogenetic process in development, which involves cell shape changes powered by mechanical forces. How mechanically interconnected tissues coordinate in organismal development remains largely unexplored. During C. elegans elongation, cyclic forces generated by muscle contractions induce remodeling of adherens junctions and the actin cytoskeleton in the epidermis, facilitating gradual embryo lengthening. While previous studies have identified key players in epidermal cells, understanding how muscle cells coordinate their activity for proper embryo elongation remains unsolved. Using a Calcium sensor to monitor muscle activity during elongation, we identified two cells in each muscle quadrant with a leader cell function that orchestrate muscle activity within their respective quadrants. Strikingly, ablation of these cells halted muscle contractions and delayed elongation. A targeted RNAi screen focusing on communication channels identified two innexins and two Deg channels regulating muscle activity, which proved required for normal embryonic elongation. Interestingly, one innexin exhibits specific expression in intestinal cells. Our findings provide novel insights into how embryonic body wall muscles coordinate their activity and how interconnected tissues ensure proper morphogenesis.</p>","PeriodicalId":11375,"journal":{"name":"Development","volume":" ","pages":""},"PeriodicalIF":3.7000,"publicationDate":"2025-03-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Muscle and intestine innexins with muscle Deg/Enac channels promote muscle coordination and embryo elongation.\",\"authors\":\"Flora Llense, Teresa Ferraro, Xinyi Yang, Hanla Song, Michel Labouesse\",\"doi\":\"10.1242/dev.204242\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Body axis elongation represents a fundamental morphogenetic process in development, which involves cell shape changes powered by mechanical forces. How mechanically interconnected tissues coordinate in organismal development remains largely unexplored. During C. elegans elongation, cyclic forces generated by muscle contractions induce remodeling of adherens junctions and the actin cytoskeleton in the epidermis, facilitating gradual embryo lengthening. While previous studies have identified key players in epidermal cells, understanding how muscle cells coordinate their activity for proper embryo elongation remains unsolved. Using a Calcium sensor to monitor muscle activity during elongation, we identified two cells in each muscle quadrant with a leader cell function that orchestrate muscle activity within their respective quadrants. Strikingly, ablation of these cells halted muscle contractions and delayed elongation. A targeted RNAi screen focusing on communication channels identified two innexins and two Deg channels regulating muscle activity, which proved required for normal embryonic elongation. Interestingly, one innexin exhibits specific expression in intestinal cells. Our findings provide novel insights into how embryonic body wall muscles coordinate their activity and how interconnected tissues ensure proper morphogenesis.</p>\",\"PeriodicalId\":11375,\"journal\":{\"name\":\"Development\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2025-03-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Development\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1242/dev.204242\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"DEVELOPMENTAL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Development","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1242/dev.204242","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"DEVELOPMENTAL BIOLOGY","Score":null,"Total":0}
Muscle and intestine innexins with muscle Deg/Enac channels promote muscle coordination and embryo elongation.
Body axis elongation represents a fundamental morphogenetic process in development, which involves cell shape changes powered by mechanical forces. How mechanically interconnected tissues coordinate in organismal development remains largely unexplored. During C. elegans elongation, cyclic forces generated by muscle contractions induce remodeling of adherens junctions and the actin cytoskeleton in the epidermis, facilitating gradual embryo lengthening. While previous studies have identified key players in epidermal cells, understanding how muscle cells coordinate their activity for proper embryo elongation remains unsolved. Using a Calcium sensor to monitor muscle activity during elongation, we identified two cells in each muscle quadrant with a leader cell function that orchestrate muscle activity within their respective quadrants. Strikingly, ablation of these cells halted muscle contractions and delayed elongation. A targeted RNAi screen focusing on communication channels identified two innexins and two Deg channels regulating muscle activity, which proved required for normal embryonic elongation. Interestingly, one innexin exhibits specific expression in intestinal cells. Our findings provide novel insights into how embryonic body wall muscles coordinate their activity and how interconnected tissues ensure proper morphogenesis.
期刊介绍:
Development’s scope covers all aspects of plant and animal development, including stem cell biology and regeneration. The single most important criterion for acceptance in Development is scientific excellence. Research papers (articles and reports) should therefore pose and test a significant hypothesis or address a significant question, and should provide novel perspectives that advance our understanding of development. We also encourage submission of papers that use computational methods or mathematical models to obtain significant new insights into developmental biology topics. Manuscripts that are descriptive in nature will be considered only when they lay important groundwork for a field and/or provide novel resources for understanding developmental processes of broad interest to the community.
Development includes a Techniques and Resources section for the publication of new methods, datasets, and other types of resources. Papers describing new techniques should include a proof-of-principle demonstration that the technique is valuable to the developmental biology community; they need not include in-depth follow-up analysis. The technique must be described in sufficient detail to be easily replicated by other investigators. Development will also consider protocol-type papers of exceptional interest to the community. We welcome submission of Resource papers, for example those reporting new databases, systems-level datasets, or genetic resources of major value to the developmental biology community. For all papers, the data or resource described must be made available to the community with minimal restrictions upon publication.
To aid navigability, Development has dedicated sections of the journal to stem cells & regeneration and to human development. The criteria for acceptance into these sections is identical to those outlined above. Authors and editors are encouraged to nominate appropriate manuscripts for inclusion in one of these sections.