{"title":"生物钟失调与干细胞老化:炎症的相互作用?","authors":"Dan Li, Yuting Tan","doi":"10.15761/jts.1000438","DOIUrl":null,"url":null,"abstract":"Aging occurs in response to many triggers, including cellular senescence, telomere attrition, DNA damage, organelle stress, oncogene activation and stem cell dysfunction [1]. Among these, the aged stem cell per sec can exhibit various aging hallmarks, such as increased DNA damage, dysregulated mitochondrial function, and less efficient protein recycling. Aged stem cell is a prime factor that undermines organismal homeostasis, which can facilitate numerous pathologies including cancer, neuropathy, sarcopenia and immunopathy [2].","PeriodicalId":74000,"journal":{"name":"Journal of translational science","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dysregulated circadian clock and aged stem cell: An inflammatory crosstalk?\",\"authors\":\"Dan Li, Yuting Tan\",\"doi\":\"10.15761/jts.1000438\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Aging occurs in response to many triggers, including cellular senescence, telomere attrition, DNA damage, organelle stress, oncogene activation and stem cell dysfunction [1]. Among these, the aged stem cell per sec can exhibit various aging hallmarks, such as increased DNA damage, dysregulated mitochondrial function, and less efficient protein recycling. Aged stem cell is a prime factor that undermines organismal homeostasis, which can facilitate numerous pathologies including cancer, neuropathy, sarcopenia and immunopathy [2].\",\"PeriodicalId\":74000,\"journal\":{\"name\":\"Journal of translational science\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of translational science\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.15761/jts.1000438\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of translational science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15761/jts.1000438","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Dysregulated circadian clock and aged stem cell: An inflammatory crosstalk?
Aging occurs in response to many triggers, including cellular senescence, telomere attrition, DNA damage, organelle stress, oncogene activation and stem cell dysfunction [1]. Among these, the aged stem cell per sec can exhibit various aging hallmarks, such as increased DNA damage, dysregulated mitochondrial function, and less efficient protein recycling. Aged stem cell is a prime factor that undermines organismal homeostasis, which can facilitate numerous pathologies including cancer, neuropathy, sarcopenia and immunopathy [2].