Human tissue inhibitor of metalloproteinases‐1 improved wound healing in diabetes through its anti‐apoptotic effect

• Published in: Experimental dermatology Vol. 28; no. 5; pp. 528 - 535
• Main Authors: Lao, Guojuan, Ren, Meng, Wang, Xiaoyi, Zhang, Jinglu, Huang, Yanrui, Liu, Dan, Luo, Hengcong, Yang, Chuan, Yan, Li
• Format: Journal Article
• Language: English
• Published: Denmark Wiley Subscription Services, Inc 01.05.2019
• Subjects: adenovirus; Advanced glycosylation end products; Animal models; Apoptosis; Diabetes; Diabetes mellitus; diabetic foot ulcer; Fibroblasts; Gene therapy; Gene transfer; Proteins; Rodents; Skin; Tissue inhibitor of metalloproteinases; tissue inhibitor of metalloproteinase‐1; Wound healing; tissue inhibitor of metalloproteinase-1; apoptosis; wound healing; diabetic foot ulcer; adenovirus
• ISSN: 0906-6705; 1600-0625; 1600-0625
• DOI: 10.1111/exd.13442

Impaired wound healing accompanies severe cell apoptosis in diabetic patients. Tissue inhibitor of metalloproteinases‐1 (TIMP‐1) was known to have effects on promoting growth and anti‐apoptosis for cells. We aimed to determine the actual levels of TIMP‐1 and cell apoptosis in: (i) the biopsies of diabetic and non‐diabetic foot tissue and (ii) the human fibroblasts with or without treatments of advanced glycation end‐products (AGEs). Next, we aimed to determine the improved levels of cell apoptosis and wound healing after the treatments of either active protein of TIMP‐1 or in vivo expression of gene therapy vector‐mediated TIMP‐1 in both the human fibroblasts and the animal model of diabetic rats. The levels of TIMP‐1 were significantly reduced in diabetic skin tissues and in AGEs‐treated fibroblasts. Both AGEs‐treated cells were effectively protected from apoptosis by active protein of TIMP‐1 at appropriate dose level. So did the induced in vivo TIMP‐1 expression after gene delivery. Similar effects were also found on the significant improvement of impaired wound healing in diabetic rats. We concluded that TIMP‐1 improved wound healing through its anti‐apoptotic effect. Treatments with either active protein TIMP‐1 or TIMP‐1 gene therapy delivered in local wound sites may be used as a strategy for accelerating diabetic wound healing.