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Chinese Journal of Injury Repair and Wound Healing(Electronic Edition) ›› 2026, Vol. 21 ›› Issue (03): 229-235. doi: 10.3877/cma.j.issn.1673-9450.2026.03.010

• Review • Previous Articles    

Application of recombinant human type Ⅲ collagen in skin wounds and scars

Yan Zeng1, Yu'an Zhu1, Zihan Tao1, Jian Jin2, Qingsong Liu2, Shihui Zhu1,2,()   

  1. 1 Department of Burn Surgery, the First Affiliated Hospital of Naval Medical University, Shanghai 200433, China
    2 Department of Burn and Plastic Surgery, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai 200127, China
  • Received:2026-02-02 Online:2026-06-01 Published:2026-06-01
  • Contact: Shihui Zhu

Abstract:

Type Ⅲ collagen (ColⅢ) is a key component of the extracellular matrix (ECM) and is crucial for maintaining the structural integrity of the skin and promoting repair. Traditional animal-derived ColⅢ has issues such as source variations, immunogenicity risks, and batch differences. Recombinant human type Ⅲ collagen (rhColⅢ), produced through genetic engineering, is highly homologous to natural ColⅢ and overcomes the risks associated with animal sources. Utilizing the biological activity of rhColⅢ, it can be prepared into various material forms such as electrospun nanofiber membranes, hydrogels, microneedle patches, and free rhColⅢ chains to promote wound healing and reduce scar formation. rhColⅢ may downregulate the expression of fibrotic genes by interfering with the transforming growth factor-β (TGF-β)/Smad signaling pathways, or enter fibroblasts through the urokinase-type plasminogen activator receptor-associated protein (uPARAP)/endocytic receptor 180 (Endo180) endocytic pathway as raw materials for synthesizing ColⅢ, directly regulating the ratio of Col Ⅰ/ColⅢ, thereby promoting wound healing. Additionally, this review explores the effects of expression systems and chemical modifications on the structure and function of rhColⅢ, and proposes suggestions for future research from perspectives such as material design, mechanism study, intervention of old scars, and clinical translation.

Key words: Collagen, Recombinant human type Ⅲ collagen, Wound healing, Scar formation

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