| Literature DB >> 27216158 |
Yoshiaki Tamura1, Naotaka Izumiyama-Shimomura2, Yoshiyuki Kimbara3, Ken-Ichi Nakamura2, Naoshi Ishikawa4,5, Junko Aida2,6, Yuko Chiba3, Yoko Matsuda6, Seijiro Mori3, Tomio Arai6, Mutsunori Fujiwara7, Steven S S Poon2,6, Tatsuro Ishizaki8, Atsushi Araki3, Kaiyo Takubo2,6, Hideki Ito3.
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.Entities:
Keywords: Aging; Alpha cell; Beta cell; Quantitative fluorescence in situ hybridization (Q-FISH); Telomere
Mesh:
Year: 2016 PMID: 27216158 PMCID: PMC5005922 DOI: 10.1007/s11357-016-9923-0
Source DB: PubMed Journal: Age (Dordr) ISSN: 0161-9152