Is the selective accumulation of oldest centrioles in stem cells the main cause of organism ageing?

Jaba Tkemaladze
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Abstract

All molecules, structures, cells of organisms are subject to destruction in the process of vital activity. In the organisms of multicellular animals and humans, the process of regeneration is always taking place: the destruction of old cells and their replacement with new ones. Cells are replaced even if the cells are in perfect condition. The earlier the body destroys the matured cells and replaces them with new ones , the younger the body is (the higher the rate of regeneration). Stem cells are the precursor cells of all differentiated cells. Asymmetric division of the mother stem cell gives rise to one, analogue of the mother, daughter cell and another daughter cell that follows a further differentiation pathway. Despite such asymmetric division, the pool of stem cells decreases over time. Moreover, the intervals between stem cell divisions are increasing. The combination of these two processes leads to a decrease in the rate of regeneration and ageing of the organism. During asymmetric division of stem cells, daughter cells, with preserved stem cell potency, selectively retain mother (old) centrioles. Unlike nuclear DNA molecules, repairs do not occur in centrioles. Hypothetically, old centrioles are more susceptible to destruction than other cell structures—making centrioles a potentially structure of the ageing of organisms.
干细胞中最老中心粒的选择性积累是生物体衰老的主要原因吗?
生物体的所有分子、结构、细胞在生命活动的过程中都会受到破坏。在多细胞动物和人类的有机体中,再生过程总是在发生:旧细胞的破坏和新细胞的替换。即使细胞处于完美状态,也要更换细胞。身体越早破坏成熟的细胞并用新的细胞代替它们,身体就越年轻(再生速度越高)。干细胞是所有分化细胞的前体细胞。母干细胞的不对称分裂产生一个类似的母细胞、子细胞和另一个遵循进一步分化途径的子细胞。尽管存在这样的不对称分裂,但干细胞池会随着时间的推移而减少。此外,干细胞分裂的间隔时间也在增加。这两个过程的结合导致生物体再生和衰老速度的下降。在干细胞的不对称分裂过程中,保留了干细胞效力的子细胞选择性地保留了母细胞(旧的)中心粒。与核DNA分子不同,修复不会发生在中心粒中。假设年老的中心粒比其他细胞结构更容易受到破坏,这使得中心粒成为生物体衰老的潜在结构。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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