Wound senescence: A functional link between diabetes and ageing?

衰老 糖基化 老化 伤口愈合 糖尿病 病态的 医学 糖基化终产物 生物 病理 免疫学 内科学 内分泌学
作者
Holly N. Wilkinson,Matthew J. Hardman
出处
期刊:Experimental Dermatology [Wiley]
卷期号:30 (1): 68-73 被引量:35
标识
DOI:10.1111/exd.14082
摘要

Arguably, the two most important causes of pathological healing in the skin are diabetes and ageing. While these factors have historically been considered independent modifiers of the healing process, recent studies suggest that they may be mechanistically linked. The primary contributor to diabetic pathology is hyperglycaemia, which accelerates the production of advanced glycation end products, a characteristic of ageing tissue. Indeed, advanced age also leads to mild hyperglycaemia. Here, we discuss emerging literature that reveals a hitherto unappreciated link between cellular senescence, diabetes and wound repair. Senescent cells cause widespread destruction of normal tissue architecture in ageing and have been shown to be increased in chronic wounds. However, the role of senescence remains controversial, with several studies reporting beneficial effects for transiently induced senescence in wound healing. We recently highlighted a direct role for senescence in diabetic healing pathology, mediated by the senescence receptor, CXCR2. These findings suggest that targeting local tissue senescence may provide a therapeutic strategy applicable to a broad range of chronic wound types.
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