Hoseini Seyed Mehdi, Montazeri Fateme
Biotechnology Research Center, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Hematology and Oncology Research Center, Non-communicable Diseases Research Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Hum Cell. 2025 Apr 12;38(3):87. doi: 10.1007/s13577-025-01213-y.
While mesenchymal stem/stromal cells (MSCs) exhibit the ability to self-renew, they are not immortal; they eventually reach a point of irreversible growth cessation and functional deterioration following a limited series of population doublings, referred to as replicative senescence. When evaluated according to the criteria set by the International Society for Cell Therapy (ISCT), MSCs show significant differences in their senescence patterns and other characteristics related to their phenotype and function. These differences are attributed to the source of the MSCs and the conditions in which they are grown. MSCs derived from fetal or adult sources have variations in their genome stability, as well as in the expression and epigenetic profile of the cells, which in turn affects their secretome. Understanding the key factors of MSC senescence based on cell source can help to develop effective strategies for regulating senescence and improving the therapeutic potential.
虽然间充质干/基质细胞(MSCs)具有自我更新能力,但它们并非永生;在经历有限次数的群体倍增后,它们最终会达到不可逆的生长停滞和功能衰退阶段,这被称为复制性衰老。根据国际细胞治疗协会(ISCT)设定的标准进行评估时,MSCs在衰老模式以及与它们的表型和功能相关的其他特征方面存在显著差异。这些差异归因于MSCs的来源以及它们生长的条件。源自胎儿或成人来源的MSCs在基因组稳定性以及细胞的表达和表观遗传谱方面存在差异,这反过来又会影响它们的分泌组。基于细胞来源了解MSCs衰老的关键因素有助于制定有效的策略来调节衰老并提高治疗潜力。