Application of adipose mesenchymal stem cell-derived exosomes-loaded β-chitin nanofiber hydrogel for wound healing

间充质干细胞 伤口愈合 外体 小桶 脂肪组织 化学 细胞生物学 转录组 微泡 生物 小RNA 生物化学 基因表达 免疫学 基因
作者
Ying Liu,Yunen Liu,Yan Zhao,Mi Wu,Shun Mao,Peifang Cong,Rufei Zou,Mingxiao Hou,Hongxu Jin,Yongli Bao
出处
期刊:Folia Histochemica Et Cytobiologica [Via Medica]
卷期号:60 (2): 167-178 被引量:16
标识
DOI:10.5603/fhc.a2022.0015
摘要

Clarifying the role and mechanism of exosome gel in wound repair can provide a new effective strategy for wound treatment.The cellular responses of adipose mesenchymal stem cell-derived exosomes (AMSC-exos) and the wound healing ability of AMSC-exos-loaded β-chitin nanofiber (β-ChNF) hydrogel were studied in vitro in mouse fibroblasts cells (L929) and in vivo in rat skin injury model. The transcriptome and proteome of rat skin were studied with the use of sequenator and LC-MS/MS, respectively.80 and 160 μg/mL AMSC-exos could promote the proliferation and migration of mouse fibroblasts cells. Furthermore, AMSC-exos-loaded β-ChNF hydrogel resulted in a significant acceleration rate of wound closure, notably acceleration of re-epithelialization, and increased collagen expression based on the rat full-thickness skin injury model. The transcriptomics and proteomics studies revealed the changes of the expression of 18 genes, 516 transcripts and 250 proteins. The metabolic pathways, tight junction, NF-κB signaling pathways were enriched in Kyoto Encyclopedia of Genes and Genomes (KEGG) Pathway. Complement factor D (CFD) and downstream Aldolase A (Aldoa) and Actn2 proteins in rats treated with AMSC-exos-loaded β-ChNF hydrogel were noticed and further confirmed by ELISA and Western blot.These findings suggested that AMSC-exos-loaded β-ChNF hydrogel could promote wound healing with the mechanism which is related to the effect of AMSC-exos on CFD and downstream proteins.
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