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Wound senescence: A functional link between diabetes and ageing?
- Source :
- Experimental Dermatology. 30:68-73
- Publication Year :
- 2020
- Publisher :
- Wiley, 2020.
-
Abstract
- 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.
- Subjects :
- 0301 basic medicine
Senescence
Chronic wound
Dermatology
Bioinformatics
Biochemistry
Receptors, Interleukin-8B
Mice
030207 dermatology & venereal diseases
03 medical and health sciences
0302 clinical medicine
Glycation
Skin Physiological Phenomena
Diabetes mellitus
Diabetes Mellitus
Animals
Humans
Medicine
CXC chemokine receptors
Molecular Biology
Pathological
Cellular Senescence
Wound Healing
business.industry
medicine.disease
Skin Aging
030104 developmental biology
Ageing
medicine.symptom
business
Wound healing
Subjects
Details
- ISSN :
- 16000625 and 09066705
- Volume :
- 30
- Database :
- OpenAIRE
- Journal :
- Experimental Dermatology
- Accession number :
- edsair.doi.dedup.....66b19f0fd89910f0501cbc9dd42ed70b
- Full Text :
- https://doi.org/10.1111/exd.14082