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Transcriptome evidence reveals enhanced autophagy-lysosomal function in centenarians

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机构: [1]State Key Laboratory of Genetic Resources and Evolution/Key Laboratory of Healthy Aging Research of Yunnan Province, KunmingInstitute of Zoology, Chinese Academy of Sciences, Kunming 650223, China [2]Center for Excellence in Animal Evolution and Genetics,Chinese Academy of Sciences, Kunming 650223, China [3]Department of Biochemistry and Molecular Biology, Hainan MedicalCollege, Haikou 571199, China [4]KIZ/CUHK Joint Laboratory of Bioresources and Molecular Research in Common Diseases, Kunming650223, China [5]Kunming College of Life Science, University of Chinese Academy of Sciences, Beijing 100049, China [6]KeyLaboratory of Animal Models and Human Disease Mechanisms of the Chinese Academy of Sciences/Key Laboratory of Healthy AgingResearch of Yunnan Province, Kunming Institute of Zoology, Kunming 650223, China [7]Kunming Key Laboratory of Healthy AgingStudy, Kunming 650223, China [8]Department of Biology, Hainan Medical College, Haikou 571199, China [9]Department ofNeurology, the First Affiliated Hospital of Hainan Medical College, Haikou 571199, China [10]Department of Chemical Pathology andLaboratory for Genetics of Disease Susceptibility, Li Ka Shing Institute of Health Sciences, and School of Biomedical Sciences, Faculty ofMedicine, The Chinese University of Hong Kong, Hong Kong 999077, China [11]Department of Pharmacology and Cancer Biology,Duke University Medical Center, Durham, North Carolina 27710, USA
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Centenarians (CENs) are excellent subjects to study the mechanisms of human longevity and healthy aging. Here, we analyzed the transcriptomes of 76 centenarians, 54 centenarian-children, and 41 spouses of centenarian-children by RNA sequencing and found that, among the significantly differentially expressed genes (SDEGs) exhibited by CENs, the autophagy-lysosomal pathway is significantly up-regulated. Overexpression of several genes from this pathway, CTSB, ATP6V0C, ATG4D, and WIPI1, could promote autophagy and delay senescence in cultured IMR-90 cells, while overexpression of the Drosophila homolog of WIPI1, Atg18a, extended the life span in transgenic flies. Interestingly, the enhanced autophagy-lysosomal activity could be partially passed on to their offspring, as manifested by their higher levels of both autophagy-encoding genes and serum beclin 1 (BECN1). In light of the normal age-related decline of autophagy-lysosomal functions, these findings provide a compelling explanation for achieving longevity in, at least, female CENs, given the gender bias in our collected samples, and suggest that the enhanced waste-cleaning activity via autophagy may serve as a conserved mechanism to prolong the life span from Drosophila to humans.© 2018 Xiao et al.; Published by Cold Spring Harbor Laboratory Press.

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出版当年[2018]版:
大类 | 1 区 生物
小类 | 1 区 生化与分子生物学 1 区 生物工程与应用微生物 1 区 遗传学
最新[2023]版:
大类 | 2 区 生物学
小类 | 1 区 生物工程与应用微生物 2 区 生化与分子生物学 2 区 遗传学
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第一作者机构: [1]State Key Laboratory of Genetic Resources and Evolution/Key Laboratory of Healthy Aging Research of Yunnan Province, KunmingInstitute of Zoology, Chinese Academy of Sciences, Kunming 650223, China [2]Center for Excellence in Animal Evolution and Genetics,Chinese Academy of Sciences, Kunming 650223, China [4]KIZ/CUHK Joint Laboratory of Bioresources and Molecular Research in Common Diseases, Kunming650223, China [7]Kunming Key Laboratory of Healthy AgingStudy, Kunming 650223, China
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通讯机构: [1]State Key Laboratory of Genetic Resources and Evolution/Key Laboratory of Healthy Aging Research of Yunnan Province, KunmingInstitute of Zoology, Chinese Academy of Sciences, Kunming 650223, China [2]Center for Excellence in Animal Evolution and Genetics,Chinese Academy of Sciences, Kunming 650223, China [4]KIZ/CUHK Joint Laboratory of Bioresources and Molecular Research in Common Diseases, Kunming650223, China [7]Kunming Key Laboratory of Healthy AgingStudy, Kunming 650223, China
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