Yoshiaki Tamura, Naotaka Izumiyama-Shimomura, Yoshiyuki Kimbara, Ken-Ichi Nakamura, Naoshi Ishikawa, Junko Aida, Yuko Chiba, Yoko Matsuda, Seijiro Mori, Tomio Arai, Mutsunori Fujiwara, Steven S S Poon, Tatsuro Ishizaki, Atsushi Araki, Kaiyo Takubo, Hideki Ito
{"title":"Telomere attrition in beta and alpha cells with age.","authors":"Yoshiaki Tamura, Naotaka Izumiyama-Shimomura, Yoshiyuki Kimbara, Ken-Ichi Nakamura, Naoshi Ishikawa, Junko Aida, Yuko Chiba, Yoko Matsuda, Seijiro Mori, Tomio Arai, Mutsunori Fujiwara, Steven S S Poon, Tatsuro Ishizaki, Atsushi Araki, Kaiyo Takubo, Hideki Ito","doi":"10.1007/s11357-016-9923-0","DOIUrl":null,"url":null,"abstract":"<p><p>We have reported telomere attrition in β and α cells of the pancreas in elderly patients with type 2 diabetes, but it has not been explored how the telomere lengths of these islet cells change according to age in normal subjects. To examine the telomere lengths of β and α cells in individuals without diabetes across a wide range of ages, we conducted measurement of the telomere lengths of human pancreatic β and α cells obtained from 104 autopsied subjects without diabetes ranging in age from 0 to 100 years. As an index of telomere lengths, the normalized telomere-centromere ratio (NTCR) was determined for β (NTCRβ) and α (NTCRα) cells by quantitative fluorescence in situ hybridization (Q-FISH). We found NTCRβ and NTCRα showed almost the same levels and both decreased according to age (p < 0.001 for both). NTCRs decreased more rapidly with age and were more widely distributed (p = 0.036 for NTCRβ, p < 0.001 for NTCRα) in subjects under 18 years of age than in subjects over 18 years. There was a positive correlation between NTCRβ and NTCRα only among adult subjects (p < 0.001). In conclusion, the telomeres of β and α cells become shortened with normal aging process. </p>","PeriodicalId":7632,"journal":{"name":"AGE","volume":"38 3","pages":"61"},"PeriodicalIF":0.0000,"publicationDate":"2016-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s11357-016-9923-0","citationCount":"11","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"AGE","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s11357-016-9923-0","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2016/5/24 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 11
Abstract
We have reported telomere attrition in β and α cells of the pancreas in elderly patients with type 2 diabetes, but it has not been explored how the telomere lengths of these islet cells change according to age in normal subjects. To examine the telomere lengths of β and α cells in individuals without diabetes across a wide range of ages, we conducted measurement of the telomere lengths of human pancreatic β and α cells obtained from 104 autopsied subjects without diabetes ranging in age from 0 to 100 years. As an index of telomere lengths, the normalized telomere-centromere ratio (NTCR) was determined for β (NTCRβ) and α (NTCRα) cells by quantitative fluorescence in situ hybridization (Q-FISH). We found NTCRβ and NTCRα showed almost the same levels and both decreased according to age (p < 0.001 for both). NTCRs decreased more rapidly with age and were more widely distributed (p = 0.036 for NTCRβ, p < 0.001 for NTCRα) in subjects under 18 years of age than in subjects over 18 years. There was a positive correlation between NTCRβ and NTCRα only among adult subjects (p < 0.001). In conclusion, the telomeres of β and α cells become shortened with normal aging process.