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组织特异性间充质干细胞衍生细胞外囊泡抗纤维化作用的比较评价及其对 CCl4 诱导的慢性肝损伤的改善作用。

Comparative Evaluation of Anti-Fibrotic Effect of Tissue Specific Mesenchymal Stem Cells Derived Extracellular Vesicles for the Amelioration of CCl4 Induced Chronic Liver Injury.

机构信息

Stem Cell Facility (DBT-Centre of Excellence for Stem Cell Research), All India Institute of Medical Sciences, 1st Floor, ORBO Complex, New Delhi, Ansari Nagar, India.

Regional Centre for Biotechnology, Faridabad, Haryana, India.

出版信息

Stem Cell Rev Rep. 2022 Mar;18(3):1097-1112. doi: 10.1007/s12015-021-10313-9. Epub 2021 Dec 2.

DOI:10.1007/s12015-021-10313-9
PMID:34859376
Abstract

Mesenchymal Stem Cells (MSCs) derived Extracellular Vesicles (EVs) have emerged as an effective candidate for amelioration of liver fibrosis. However, the effect and the mechanisms of MSC-EVs in liver repair remains elusive. In this study, we have evaluated the differential regenerative efficacy of EVs derived from two different human tissue-specific MSCs (Adipose tissue; AD-MSC and Wharton's Jelly; WJ-MSC), in a murine model of chronic liver fibrosis. Mouse model of chronic liver injury was induced by carbon tetrachloride (CCl) injection, followed by administration of EVs via the tail vein. Both quantitative and qualitative assessment was done to evaluate the hepatic regenerative potential of tissue specific MSC-extracellular vesicles. EVs, regardless of their MSC source, were found to be effective in alleviating chronic liver fibrosis, as demonstrated by macroscopic alterations in the liver. According to the findings of the comprehensive study, there were subtle variations in the tissue specific MSCs-EVs mediated approaches. A greater anti-fibrotic impact was demonstrated by AD-MSC derived EVs through extracellular matrix alteration and hepatocyte proliferation. WJ-MSC EVs, on the other hand, have an anti-inflammatory effect, as evidenced by alterations in the expression of pro- and anti-inflammatory cytokines. Furthermore, cargo profiling of these EVs revealed differences in the miRNA and protein expression, as well as the pathways that they were associated. Comparative overview of regression of fibrosis using tissue specific MSC derived EVs (credits BioRender.com ).

摘要

间充质干细胞(MSCs)衍生的细胞外囊泡(EVs)已成为改善肝纤维化的有效候选物。然而,MSC-EVs 在肝脏修复中的作用和机制仍不清楚。在这项研究中,我们评估了两种不同的组织特异性 MSC(脂肪组织;AD-MSC 和 Wharton 胶;WJ-MSC)衍生的 EV 在慢性肝纤维化的小鼠模型中的差异再生疗效。通过四氯化碳(CCl)注射诱导慢性肝损伤小鼠模型,然后通过尾静脉给予 EV。进行了定量和定性评估,以评估组织特异性 MSC-细胞外囊泡的肝再生潜力。无论其 MSC 来源如何,EV 都被发现能有效缓解慢性肝纤维化,这可通过肝脏的宏观改变得到证实。根据综合研究的结果,组织特异性 MSC-EVs 介导的方法存在细微差异。AD-MSC 衍生的 EV 通过细胞外基质改变和肝细胞增殖显示出更强的抗纤维化作用。另一方面,WJ-MSC EV 具有抗炎作用,这表现在促炎和抗炎细胞因子表达的改变。此外,这些 EV 的货物分析揭示了 miRNA 和蛋白质表达以及它们相关的途径存在差异。使用组织特异性 MSC 衍生的 EV 进行纤维化消退的比较概述(来源 BioRender.com )。

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