{"title":"脑积水模型中Ccdc85c基因敲除大鼠神经发生、胶质瘤发生和室管膜形成被破坏","authors":"Md. Mehedi Hasan, Shizuka Konishi, Miyuu Tanaka, Takeshi Izawa, Jyoji Yamate, Mitsuru Kuwamura","doi":"10.1016/j.cdev.2023.203858","DOIUrl":null,"url":null,"abstract":"<div><p>Coil-coiled domain containing 85c (<em>Ccdc85c</em><span>) is a causative gene for congenital hydrocephalus and subcortical heterotopia with frequent brain hemorrhage. We established </span><em>Ccdc85c</em><span><span><span> knockout (KO) rats and investigated the roles of CCDC85C and intermediate filament<span> protein expression, including </span></span>nestin<span>, vimentin, GFAP, and </span></span>cytokeratin<span> AE1/AE3 during the lateral ventricle<span> development in KO rats to evaluate the role of this gene. We found altered and ectopic expression<span><span> of nestin and vimentin positive cells in the wall of the dorso-lateral ventricle in the KO rats during development from the age of postnatal day (P) 6, whereas both protein expression became faint in the wild-type rats. In the KO rats, there was a loss of cytokeratin expression on the surface of the dorso-lateral ventricle with ectopic expression and maldevelopment of ependymal cells<span>. Our data also revealed disturbed GFAP expression at postnatal ages. These findings indicate that lack of CCDC85C disrupts the proper expression of intermediate filament proteins (nestin, vimentin, GFAP, and cytokeratin), and CCDC85C is necessary for normal neurogenesis, </span></span>gliogenesis, and ependymogenesis.</span></span></span></span></p></div>","PeriodicalId":36123,"journal":{"name":"Cells and Development","volume":"175 ","pages":"Article 203858"},"PeriodicalIF":3.9000,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Disrupted neurogenesis, gliogenesis, and ependymogenesis in the Ccdc85c knockout rat for hydrocephalus model\",\"authors\":\"Md. Mehedi Hasan, Shizuka Konishi, Miyuu Tanaka, Takeshi Izawa, Jyoji Yamate, Mitsuru Kuwamura\",\"doi\":\"10.1016/j.cdev.2023.203858\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Coil-coiled domain containing 85c (<em>Ccdc85c</em><span>) is a causative gene for congenital hydrocephalus and subcortical heterotopia with frequent brain hemorrhage. We established </span><em>Ccdc85c</em><span><span><span> knockout (KO) rats and investigated the roles of CCDC85C and intermediate filament<span> protein expression, including </span></span>nestin<span>, vimentin, GFAP, and </span></span>cytokeratin<span> AE1/AE3 during the lateral ventricle<span> development in KO rats to evaluate the role of this gene. We found altered and ectopic expression<span><span> of nestin and vimentin positive cells in the wall of the dorso-lateral ventricle in the KO rats during development from the age of postnatal day (P) 6, whereas both protein expression became faint in the wild-type rats. In the KO rats, there was a loss of cytokeratin expression on the surface of the dorso-lateral ventricle with ectopic expression and maldevelopment of ependymal cells<span>. Our data also revealed disturbed GFAP expression at postnatal ages. These findings indicate that lack of CCDC85C disrupts the proper expression of intermediate filament proteins (nestin, vimentin, GFAP, and cytokeratin), and CCDC85C is necessary for normal neurogenesis, </span></span>gliogenesis, and ependymogenesis.</span></span></span></span></p></div>\",\"PeriodicalId\":36123,\"journal\":{\"name\":\"Cells and Development\",\"volume\":\"175 \",\"pages\":\"Article 203858\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2023-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cells and Development\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2667290123000347\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Biochemistry, Genetics and Molecular Biology\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cells and Development","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667290123000347","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
Disrupted neurogenesis, gliogenesis, and ependymogenesis in the Ccdc85c knockout rat for hydrocephalus model
Coil-coiled domain containing 85c (Ccdc85c) is a causative gene for congenital hydrocephalus and subcortical heterotopia with frequent brain hemorrhage. We established Ccdc85c knockout (KO) rats and investigated the roles of CCDC85C and intermediate filament protein expression, including nestin, vimentin, GFAP, and cytokeratin AE1/AE3 during the lateral ventricle development in KO rats to evaluate the role of this gene. We found altered and ectopic expression of nestin and vimentin positive cells in the wall of the dorso-lateral ventricle in the KO rats during development from the age of postnatal day (P) 6, whereas both protein expression became faint in the wild-type rats. In the KO rats, there was a loss of cytokeratin expression on the surface of the dorso-lateral ventricle with ectopic expression and maldevelopment of ependymal cells. Our data also revealed disturbed GFAP expression at postnatal ages. These findings indicate that lack of CCDC85C disrupts the proper expression of intermediate filament proteins (nestin, vimentin, GFAP, and cytokeratin), and CCDC85C is necessary for normal neurogenesis, gliogenesis, and ependymogenesis.