https://transhumanist.ru/index.php?action=history&feed=atom&title=MDC1 2026-04-13T15:40:32Z История изменений этой страницы в вики MediaWiki 1.43.6 https://transhumanist.ru/index.php?title=MDC1&diff=5503&oldid=prev 2021-05-12T13:46:58Z

<p>Новая страница: «Mediator of DNA damage checkpoint protein 1 (Nuclear factor with BRCT domains 1) [KIAA0170] [NFBD1] ==Publications== {{medline-entry |title=Accumulation of DNA...»</p> <p><b>Новая страница</b></p><div>Mediator of DNA damage checkpoint protein 1 (Nuclear factor with BRCT domains 1) [KIAA0170] [NFBD1]<br /> <br /> ==Publications==<br /> <br /> {{medline-entry<br /> |title=Accumulation of DNA damage in hematopoietic stem and progenitor cells during human aging.<br /> |pubmed-url=https://pubmed.ncbi.nlm.nih.gov/21408175<br /> |abstract=Accumulation of DNA damage leading to adult stem cell exhaustion has been proposed to be a principal mechanism of aging. Here we tested this hypothesis in healthy individuals of different ages by examining unrepaired DNA double-strand breaks (DSBs) in hematopoietic stem/progenitor cells matured in their physiological microenvironment. To asses DNA damage accumulation and repair capacities, γH2AX-foci were examined before and after exposure to ionizing irradiation. Analyzing [[CD34]] and [[CD34]]- stem/progenitor cells we observed an increase of endogenous γH2AX-foci levels with advancing donor age, associated with an age-related decline in telomere length. Using combined immunofluorescence and telomere-fluorescence in-situ hybridization we show that γH2AX-foci co-localize consistently with other repair factors such as pATM, [[MDC1]] and 53BP1, but not significantly with telomeres, strongly supporting the telomere-independent origin for the majority of foci. The highest inter-individual variations for non-telomeric DNA damage were observed in middle-aged donors, whereas the individual DSB repair capacity appears to determine the extent of DNA damage accrual. However, analyzing different stem/progenitor subpopulations obtained from healthy elderly (&gt;70 years), we observed an only modest increase in DNA damage accrual, most pronounced in the primitive [[CD34]] CD38(-)-enriched subfraction, but sustained DNA repair efficiencies, suggesting that healthy lifestyle may slow down the natural aging process. Based on these findings we conclude that age-related non-telomeric DNA damage accrual accompanies physiological stem cell aging in humans. Moreover, aging may alter the functional capacity of human stem cells to repair DSBs, thereby deteriorating an important genome protection mechanism leading to exceeding DNA damage accumulation. However, the great inter-individual variations in middle-aged individuals suggest that additional cell-intrinsic mechanisms and/or extrinsic factors contribute to the age-associated DNA damage accumulation.<br /> |mesh-terms=* Adolescent<br /> * Adult<br /> * Aged<br /> * Aged, 80 and over<br /> * Aging<br /> * DNA Breaks, Double-Stranded<br /> * DNA Damage<br /> * DNA Repair<br /> * Health<br /> * Hematopoietic Stem Cells<br /> * Histones<br /> * Humans<br /> * Middle Aged<br /> * Telomere<br /> * Young Adult<br /> <br /> |full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3049780<br /> }}</div>

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