Nicola S.L. Foister, Ceri E. Oldreive, John B. Mackie, Gayle H. Doherty
{"title":"胚胎小脑颗粒细胞对同型半胱氨酸诱导的坏死具有抵抗性","authors":"Nicola S.L. Foister, Ceri E. Oldreive, John B. Mackie, Gayle H. Doherty","doi":"10.1016/j.devbrainres.2005.07.011","DOIUrl":null,"url":null,"abstract":"<div><p>Hyperhomocysteinemia is a risk factor for a range of neurodegenerative conditions, yet its effects in the developing nervous system have been poorly elucidated. We studied the in vitro response of cerebellar granule neurons (CGCs) to homocysteine<span>. We have shown that embryonic CGCs<span> are resistant to homocysteine-induced neurotoxicity, whilst postnatal CGCs are not. This is the first demonstration of a neuronal population undergoing a developmental switch in their response to homocysteine. Greater understanding of this change may have important implications for both neurodegenerative conditions and neurodevelopmental disorders.</span></span></p></div>","PeriodicalId":100369,"journal":{"name":"Developmental Brain Research","volume":"160 1","pages":"Pages 85-89"},"PeriodicalIF":0.0000,"publicationDate":"2005-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.devbrainres.2005.07.011","citationCount":"13","resultStr":"{\"title\":\"Embryonic cerebellar granule cells are resistant to necrosis induced by homocysteine\",\"authors\":\"Nicola S.L. Foister, Ceri E. Oldreive, John B. Mackie, Gayle H. Doherty\",\"doi\":\"10.1016/j.devbrainres.2005.07.011\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Hyperhomocysteinemia is a risk factor for a range of neurodegenerative conditions, yet its effects in the developing nervous system have been poorly elucidated. We studied the in vitro response of cerebellar granule neurons (CGCs) to homocysteine<span>. We have shown that embryonic CGCs<span> are resistant to homocysteine-induced neurotoxicity, whilst postnatal CGCs are not. This is the first demonstration of a neuronal population undergoing a developmental switch in their response to homocysteine. Greater understanding of this change may have important implications for both neurodegenerative conditions and neurodevelopmental disorders.</span></span></p></div>\",\"PeriodicalId\":100369,\"journal\":{\"name\":\"Developmental Brain Research\",\"volume\":\"160 1\",\"pages\":\"Pages 85-89\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2005-11-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.devbrainres.2005.07.011\",\"citationCount\":\"13\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Developmental Brain Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0165380605002130\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Developmental Brain Research","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0165380605002130","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Embryonic cerebellar granule cells are resistant to necrosis induced by homocysteine
Hyperhomocysteinemia is a risk factor for a range of neurodegenerative conditions, yet its effects in the developing nervous system have been poorly elucidated. We studied the in vitro response of cerebellar granule neurons (CGCs) to homocysteine. We have shown that embryonic CGCs are resistant to homocysteine-induced neurotoxicity, whilst postnatal CGCs are not. This is the first demonstration of a neuronal population undergoing a developmental switch in their response to homocysteine. Greater understanding of this change may have important implications for both neurodegenerative conditions and neurodevelopmental disorders.