4.7 Article

Human umbilical cord mesenchymal stem cells-derived exosomes for treating traumatic pancreatitis in rats

期刊

STEM CELL RESEARCH & THERAPY
卷 13, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s13287-022-02893-1

关键词

Exosomes; Human umbilical cord mesenchymal stem cells; Traumatic pancreatitis; Apoptosis; Inflammation; Therapeutic effect

资金

  1. Hospital Management of the General Hospital of Western Theater Command [2021-XZYG-B16]
  2. Key Research and Development Program of Sichuan Provincial Science and Technology Department [2022YFS0195]
  3. National Clinical Key Subject of China [41732113]
  4. Pancreatic Injury and Repair Key Laboratory of Sichuan Province [41732152]

向作者/读者索取更多资源

In this study, it was found that human umbilical cord mesenchymal stem cells-exosomes (hucMSC-Exs) can colonize injured pancreatic tissue and facilitate the repair of pancreatic tissue by inhibiting cell apoptosis and controlling inflammatory response.
Background The therapeutic and protective effects of human umbilical cord mesenchymal stem cells-exosomes (hucMSC-Exs) on traumatic pancreatitis (TP) remain unknown. Here, we established a rat model of TP and evaluated and compared the therapeutic effects of hUC-MSCs and hucMSC-Exs. Methods HucMSC-Exs were obtained by ultracentrifugation and identified using transmission electron microscopy and western blot analysis. TP rats were treated by tail vein injection of hUC-MSCs and hucMSC-Exs. Their homing in rats was observed by performing fluorescence microscopy. The degree of pancreatic tissue damage was assessed by HE staining, the expression levels of amylase, lipase, and inflammatory cytokines were detected by ELISA, apoptosis was detected by TUNEL assay, and the expression levels of various apoptosis-related proteins were detected by western-blot. The expression levels of apoptosis-related molecular markers were detected by RT-qPCR. Results The colonization of exosomes was observed in pancreatic tissue. Compared to TP group, the histopathological score of pancreas was significantly decreased in the TP + hUC-MSCs group and TP + hucMSC-Exs group (P < 0.05). Compared to TP group, the activity of serum amylase and lipase was significantly decreased (P < 0.05). The expression levels of IL-6 and TNF-alpha were significantly decreased, while those of IL-10 and TGF-beta were significantly increased (P < 0.05). The apoptosis index of the TP group was significantly increased (P < 0.05), whereas that of the TP + hUC-MSCs and TP + hucMSC-Exs groups was significantly decreased (P < 0.05). Compared to TP group, the expression levels of Bax, Bcl-2, and Caspase-3 were significantly decreased in the TP + hUC-MSCs group and TP + hucMSC-Exs group (P < 0.05). Conclusion HucMSC-Exs can colonize injured pancreatic tissue, inhibit the apoptosis of acinar cells, and control the systemic inflammatory response to facilitate the repair of pancreatic tissue.

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