Department of Plastic & Reconstructive Surgery, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, 200011, Shanghai, China.
Cell Death Dis. 2022 Apr 4;13(4):300. doi: 10.1038/s41419-022-04752-6.
Adipose tissue, which is the crucial energy reservoir and endocrine organ for the maintenance of systemic glucose, lipid, and energy homeostasis, undergoes significant changes during aging. These changes cause physiological declines and age-related disease in the elderly population. Here, we review the age-related changes in adipose tissue at multiple levels and highlight the underlying mechanisms regulating the aging process. We also discuss the pathogenic pathways of age-related fat dysfunctions and their systemic negative consequences, such as dyslipidemia, chronic general inflammation, insulin resistance, and type 2 diabetes (T2D). Age-related changes in adipose tissue involve redistribution of deposits and composition, in parallel with the functional decline of adipocyte progenitors and accumulation of senescent cells. Multiple pathogenic pathways induce defective adipogenesis, inflammation, aberrant adipocytokine production, and insulin resistance, leading to adipose tissue dysfunction. Changes in gene expression and extracellular signaling molecules regulate the aging process of adipose tissue through various pathways. In addition, adipose tissue aging impacts other organs that are infiltrated by lipids, which leads to systemic inflammation, metabolic system disruption, and aging process acceleration. Moreover, studies have indicated that adipose aging is an early onset event in aging and a potential target to extend lifespan. Together, we suggest that adipose tissue plays a key role in the aging process and is a therapeutic target for the treatment of age-related disease, which deserves further study to advance relevant knowledge.
脂肪组织是维持全身葡萄糖、脂质和能量稳态的关键能量储存库和内分泌器官,在衰老过程中会发生显著变化。这些变化导致老年人的生理衰退和与年龄相关的疾病。在这里,我们综述了脂肪组织在多个层面上的与年龄相关的变化,并强调了调节衰老过程的潜在机制。我们还讨论了与年龄相关的脂肪功能障碍的发病途径及其对全身的负面影响,如血脂异常、慢性全身炎症、胰岛素抵抗和 2 型糖尿病(T2D)。脂肪组织的与年龄相关的变化涉及到沉积和组成的重新分布,同时伴随着脂肪细胞祖细胞功能下降和衰老细胞的积累。多种致病途径导致脂肪生成缺陷、炎症、异常脂肪细胞因子产生和胰岛素抵抗,从而导致脂肪组织功能障碍。基因表达和细胞外信号分子的变化通过多种途径调节脂肪组织的衰老过程。此外,脂肪组织的衰老会影响到被脂肪浸润的其他器官,导致全身炎症、代谢系统紊乱和衰老过程加速。此外,研究表明,脂肪组织衰老在衰老过程中是一个早期事件,也是延长寿命的一个潜在靶点。总之,我们认为脂肪组织在衰老过程中起着关键作用,是治疗与年龄相关疾病的一个治疗靶点,值得进一步研究以推进相关知识。