Metabolic reprogramming in skin wound healing

Author:

Wang Zitong1ORCID,Zhao Feng23,Xu Chengcheng1,Zhang Qiqi1,Ren Haiyue1ORCID,Huang Xing4,He Cai1,Ma Jiajie1,Wang Zhe1ORCID

Affiliation:

1. Department of Pathology, Shengjing Hospital of China Medical University , Shenyang, No. 36 Sanhao Street, Shenyang, 110004 , China

2. Department of Stem Cells and Regenerative Medicine , Shenyang Key Laboratory of Stem Cell and Regenerative Medicine, , No. 77 Puhe Road, Shenyang, 110013 , China

3. China Medical University , Shenyang Key Laboratory of Stem Cell and Regenerative Medicine, , No. 77 Puhe Road, Shenyang, 110013 , China

4. Department of General Surgery, Shengjing Hospital of China Medical University , No. 36 Sanhao Street, Shenyang, 110004 , China

Abstract

Abstract Metabolic reprogramming refers to the ability of a cell to alter its metabolism in response to different stimuli and forms of pressure. It helps cells resist external stress and provides them with new functions. Skin wound healing involves the metabolic reprogramming of nutrients, such as glucose, lipids, and amino acids, which play vital roles in the proliferation, differentiation, and migration of multiple cell types. During the glucose metabolic process in wounds, glucose transporters and key enzymes cause elevated metabolite levels. Glucose-mediated oxidative stress drives the proinflammatory response and promotes wound healing. Reprogramming lipid metabolism increases the number of fibroblasts and decreases the number of macrophages. It enhances local neovascularization and improves fibrin stability to promote extracellular matrix remodelling, accelerates wound healing, and reduces scar formation. Reprogramming amino acid metabolism affects wound re-epithelialization, collagen deposition, and angiogenesis. However, comprehensive reviews on the role of metabolic reprogramming in skin wound healing are lacking. Therefore, we have systematically reviewed the metabolic reprogramming of glucose, lipids, and amino acids during skin wound healing. Notably, we identified their targets with potential therapeutic value and elucidated their mechanisms of action.

Funder

National Natural Science Foundation of China

345 Talent Project of Shengjing Hospital of China Medical University

Publisher

Oxford University Press (OUP)

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