Wojda Alina, Witt Michał
Institute of Human Genetics, Polish Academy of Sciences, ul. Strzeszyńska 32, 60-479 Poznań, Poland.
J Appl Genet. 2003;44(3):383-99.
The effects of ageing in humans appear to be a combination of influence of genetically programmed phenomena and exogenous environmental factors, and take place at the cellular level (senescence), rather than at the level of the organism. There are many processes, which occur in somatic cells as a consequence of DNA replication (accumulation of DNA errors or mutations that outstrip repair processes, telomere shortening, deregulation of apoptosis, etc.) and which drive replicative senescence in human cells. DNA errors are considered to be critical primary lesions in the formation of chromosomal aberrations. It can be concluded that the chromosome aberrations are biomarkers of ageing in human cells. Studies of human metaphases, interphase nuclei and micronuclei showed the increase in loss of chromosomes and the increase in frequency of stable chromosome aberrations as a function of age.
人类衰老的影响似乎是基因编程现象和外源性环境因素共同作用的结果,且发生在细胞水平(细胞衰老),而非生物体水平。由于DNA复制(DNA错误或突变积累超过修复过程、端粒缩短、细胞凋亡失调等),体细胞中会发生许多过程,这些过程推动人类细胞的复制性衰老。DNA错误被认为是染色体畸变形成中的关键原发性损伤。可以得出结论,染色体畸变是人类细胞衰老的生物标志物。对人类中期细胞、间期细胞核和微核的研究表明,随着年龄增长,染色体丢失增加,稳定染色体畸变频率上升。