Application of extracellular matrix cross-linked by microbial transglutaminase to promote wound healing

细胞外基质 伤口愈合 组织工程 组织谷氨酰胺转胺酶 化学 生物相容性 生物医学工程 脚手架 羟脯氨酸 戊二醛 Ⅰ型胶原 生物化学 外科 医学 病理 有机化学 色谱法
作者
Chenkai You,Zhihan Zhang,Yuandong Guo,Shuang Liu,Kang‐Di Hu,Yuhang Zhan,Shami· Aihemaiti,Shengxiang Tao,Yingying Chu,Lihong Fan
出处
期刊:International Journal of Biological Macromolecules [Elsevier BV]
卷期号:266 (Pt 2): 131384-131384 被引量:16
标识
DOI:10.1016/j.ijbiomac.2024.131384
摘要

One primary focus of skin tissue engineering has been the creation of innovative biomaterials to facilitate rapid wound healing. Extracellular matrix (ECM), an essential biofunctional substance, has recently been discovered to play a crucial role in wound healing. Consequently, we endeavored to decellularize ECM from pig achilles tendon and refine its mechanical and biological properties through modification by utilizing cross-linking agents. Glutaraldehyde (GA), 1-ethyl-(3-dimethylaminopropyl) carbodiimide/N-hydroxysuccinimide (EDC/NHS), double aldol starch (DAS), and microbial transglutaminase (MTG) were utilized to produce crosslinked ECM variants (GA-ECM, EDC/NHS-ECM, DAS-ECM, and MTG-ECM). Comprehensive assessments were conducted to evaluate the physical properties, biocompatibility, and wound healing efficacy of each material. The results indicated that MTG-ECM exhibited superior tensile strength, excellent hydrophilicity, minimal cytotoxicity, and the best pro-healing impact among the four modified scaffolds. Staining analysis of tissue sections further revealed that MTG-ECM impeded the transition from type III collagen to type I collagen in the wound area, potentially reducing the development of wound scar. Therefore, MTG-ECM is expected to be a potential pro-skin repair scaffold material to prevent scar formation.
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