{"title":"文昌鱼消化道的单细胞分析揭示了脊索动物中内分泌细胞的保存","authors":"Yichen Dai, Rongrong Pan, Qi Pan, Xiaotong Wu, Zexin Cai, Yongheng Fu, Chenggang Shi, Yuyu Sheng, Jingjing Li, Zhe Lin, Gaoming Liu, Pingfen Zhu, Meng Li, Guang Li, Xuming Zhou","doi":"10.1126/sciadv.adq0702","DOIUrl":null,"url":null,"abstract":"<div >Despite their pivotal role, the evolutionary origins of vertebrate digestive systems remain enigmatic. We explored the cellular characteristics of the amphioxus (<i>Branchiostoma floridae</i>) digestive tract, a model for the presumed primitive chordate digestive system, using bulk tissue companioned with single-cell RNA sequencing. Our findings reveal segmentation and a rich diversity of cell clusters, and we highlight the presence of epithelial-like, ciliated cells in the amphioxus midgut and describe three types of endocrine-like cells that secrete insulin-like, glucagon-like, and somatostatin-like peptides. Furthermore, <i>Pdx</i>, <i>Ilp1</i>, <i>Ilp2</i>, and <i>Ilpr</i> knockout amphioxus lines revealed that, in amphioxus, <i>Pdx</i> does not influence <i>Ilp</i> expression. We also unravel similarity between amphioxus Ilp1 and vertebrate insulin-like growth factor 1 (Igf1) in terms of predicted structure, effects on body growth and amino acid metabolism, and interactions with Igf-binding proteins. These findings indicate that the evolutionary alterations involving the regulatory influence of Pdx over <i>insulin</i> gene expression could have been instrumental in the development of the vertebrate digestive system.</div>","PeriodicalId":21609,"journal":{"name":"Science Advances","volume":"10 51","pages":""},"PeriodicalIF":11.7000,"publicationDate":"2024-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.science.org/doi/reader/10.1126/sciadv.adq0702","citationCount":"0","resultStr":"{\"title\":\"Single-cell profiling of the amphioxus digestive tract reveals conservation of endocrine cells in chordates\",\"authors\":\"Yichen Dai, Rongrong Pan, Qi Pan, Xiaotong Wu, Zexin Cai, Yongheng Fu, Chenggang Shi, Yuyu Sheng, Jingjing Li, Zhe Lin, Gaoming Liu, Pingfen Zhu, Meng Li, Guang Li, Xuming Zhou\",\"doi\":\"10.1126/sciadv.adq0702\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div >Despite their pivotal role, the evolutionary origins of vertebrate digestive systems remain enigmatic. We explored the cellular characteristics of the amphioxus (<i>Branchiostoma floridae</i>) digestive tract, a model for the presumed primitive chordate digestive system, using bulk tissue companioned with single-cell RNA sequencing. Our findings reveal segmentation and a rich diversity of cell clusters, and we highlight the presence of epithelial-like, ciliated cells in the amphioxus midgut and describe three types of endocrine-like cells that secrete insulin-like, glucagon-like, and somatostatin-like peptides. Furthermore, <i>Pdx</i>, <i>Ilp1</i>, <i>Ilp2</i>, and <i>Ilpr</i> knockout amphioxus lines revealed that, in amphioxus, <i>Pdx</i> does not influence <i>Ilp</i> expression. We also unravel similarity between amphioxus Ilp1 and vertebrate insulin-like growth factor 1 (Igf1) in terms of predicted structure, effects on body growth and amino acid metabolism, and interactions with Igf-binding proteins. These findings indicate that the evolutionary alterations involving the regulatory influence of Pdx over <i>insulin</i> gene expression could have been instrumental in the development of the vertebrate digestive system.</div>\",\"PeriodicalId\":21609,\"journal\":{\"name\":\"Science Advances\",\"volume\":\"10 51\",\"pages\":\"\"},\"PeriodicalIF\":11.7000,\"publicationDate\":\"2024-12-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.science.org/doi/reader/10.1126/sciadv.adq0702\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Science Advances\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://www.science.org/doi/10.1126/sciadv.adq0702\",\"RegionNum\":1,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science Advances","FirstCategoryId":"103","ListUrlMain":"https://www.science.org/doi/10.1126/sciadv.adq0702","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
Single-cell profiling of the amphioxus digestive tract reveals conservation of endocrine cells in chordates
Despite their pivotal role, the evolutionary origins of vertebrate digestive systems remain enigmatic. We explored the cellular characteristics of the amphioxus (Branchiostoma floridae) digestive tract, a model for the presumed primitive chordate digestive system, using bulk tissue companioned with single-cell RNA sequencing. Our findings reveal segmentation and a rich diversity of cell clusters, and we highlight the presence of epithelial-like, ciliated cells in the amphioxus midgut and describe three types of endocrine-like cells that secrete insulin-like, glucagon-like, and somatostatin-like peptides. Furthermore, Pdx, Ilp1, Ilp2, and Ilpr knockout amphioxus lines revealed that, in amphioxus, Pdx does not influence Ilp expression. We also unravel similarity between amphioxus Ilp1 and vertebrate insulin-like growth factor 1 (Igf1) in terms of predicted structure, effects on body growth and amino acid metabolism, and interactions with Igf-binding proteins. These findings indicate that the evolutionary alterations involving the regulatory influence of Pdx over insulin gene expression could have been instrumental in the development of the vertebrate digestive system.
期刊介绍:
Science Advances, an open-access journal by AAAS, publishes impactful research in diverse scientific areas. It aims for fair, fast, and expert peer review, providing freely accessible research to readers. Led by distinguished scientists, the journal supports AAAS's mission by extending Science magazine's capacity to identify and promote significant advances. Evolving digital publishing technologies play a crucial role in advancing AAAS's global mission for science communication and benefitting humankind.