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首页> 外文期刊>Clinical and experimental pharmacology & physiology >Transplantation of human umbilical mesenchymal stem cells attenuates dextran sulfate sodium-induced colitis in mice
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Transplantation of human umbilical mesenchymal stem cells attenuates dextran sulfate sodium-induced colitis in mice

机译:人脐带间充质干细胞的移植减轻小鼠硫酸右旋糖酐钠诱发的结肠炎

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摘要

Summary: Ulcerative colitis is a major form of inflammatory bowel disease and increases the risk of the development of colorectal carcinoma. The anti-inflammatory and immunomodulatory properties of mesenchymal stem cells (MSC) make them promising tools for treating immune-mediated and inflammatory diseases. However, the lack of robust technique for harvesting and expanding of MSC has hampered the use of bone marrow and umbilical cord blood derived MSC in clinical applications. In the present study, we investigated the intestinal protective effects of Wharton's jelly-derived umbilical MSC (UMSC) on dextran sulfate sodium-induced colitis in mice. The severity of colitis in mice was assessed using bodyweight loss, stool consistency, rectal bleeding, colon shortening and haematological parameters. Colonic myeloperoxidase and pro-inflammatory cytokines levels were also measured. Furthermore, the expression of cyclooxygenase 2 and inducible nitric oxide synthase in the colon were detected. In addition, intestinal permeability and tight junction proteins expressions in the colon were examined as well. The results showed that Wharton's jelly-derived UMSC significantly diminished the severity of colitis, reduced histolopathological score, and decreased myeloperoxidase activity and cytokines levels. Furthermore, the UMSC markedly decreased the expression of cyclooxygenase 2and inducible nitric oxide synthase in the colon. In addition, transplantation of UMSC reduced intestinal permeability and upregulated the expression of tight junction proteins. These results show that the anti-inflammation and regulation of tight junction proteins by Wharton's jelly-derived UMSC ameliorates colitis.
机译:摘要:溃疡性结肠炎是炎症性肠病的主要形式,并增加了结直肠癌发展的风险。间充质干细胞(MSC)的抗炎和免疫调节特性使其成为治疗免疫介导的炎性疾病的有前途的工具。但是,缺乏用于收获和扩增MSC的可靠技术阻碍了在临床应用中使用骨髓和脐带血来源的MSC。在本研究中,我们调查了沃顿氏胶冻脐带MSC(UMSC)对小鼠右旋糖酐硫酸钠诱导的结肠炎的肠道保护作用。使用体重减轻,粪便稠度,直肠出血,结肠缩短和血液学参数评估小鼠结肠炎的严重程度。还测量了结肠髓过氧化物酶和促炎细胞因子水平。此外,检测到结肠中环氧合酶2和诱导型一氧化氮合酶的表达。另外,还检查了结肠中的肠通透性和紧密连接蛋白表达。结果表明,沃顿商学院的果冻来源的UMSC显着降低了结肠炎的严重程度,降低了组织病理学评分,并降低了髓过氧化物酶活性和细胞因子水平。此外,UMSC明显降低了结肠中环氧合酶2和诱导型一氧化氮合酶的表达。另外,UMSC的移植降低了肠的通透性并上调了紧密连接蛋白的表达。这些结果表明,沃顿氏胶源的UMSC对紧密连接蛋白的抗炎和调节作用可改善结肠炎。

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