Robert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, Minnesota, USA.
Curr Opin Clin Nutr Metab Care. 2014 Jul;17(4):324-8. doi: 10.1097/MCO.0000000000000065.
Possible mechanisms in cellular senescence and the senescence-associated secretory phenotype (SASP) that drive and promote chronic inflammation in multiple age-related chronic diseases are considered.
A series of studies about the SASP indicate that senescent cells may be involved in the development of chronic inflammatory diseases associated with aging.
Aging is a complex biological process accompanied by a state of chronic, low-grade, 'sterile' inflammation, which is a major contributor to the development of many age-related chronic disorders including atherosclerosis, osteoarthritis, Alzheimer's disease, type 2 diabetes, cancers, and others. It appears that cellular senescence plays a role in causing inflammation through the SASP. A better understanding of the contribution of senescent cells to the pathologies of chronic inflammatory disorders could have potentially profound diagnostic and therapeutic implications.
探讨细胞衰老和衰老相关分泌表型(SASP)中可能的机制,这些机制驱动和促进多种与年龄相关的慢性疾病中的慢性炎症。
一系列关于 SASP 的研究表明,衰老细胞可能参与了与衰老相关的慢性炎症性疾病的发展。
衰老是一个复杂的生物学过程,伴随着一种慢性、低水平、“无菌”炎症的状态,这是许多与年龄相关的慢性疾病发展的主要因素,包括动脉粥样硬化、骨关节炎、阿尔茨海默病、2 型糖尿病、癌症等。细胞衰老似乎通过 SASP 在引起炎症中起作用。更好地了解衰老细胞对慢性炎症性疾病病理的贡献可能具有潜在的深远的诊断和治疗意义。