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Exogenous mesenchymal stem cells affect the function of endogenous lung stem cells (club cells) in phosgene-induced lung injury

机译:外源间充质干细胞影响内源性肺部干细胞(俱乐部细胞)在光学诱导的肺损伤中的功能

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Exogenous mesenchymal stem cells (MSCs) affect lung cells via cytokines as well as vesicles and activate the Notch signaling pathway thus affecting the proliferation of endogenous stem cells to repair damaged tissue. Club cells are endogenous lung stem cells whose proliferation is also closely related to the Notch signaling pathway. The club cell secretory protein (CCSP) has anti-inflammatory and anti-oxidative properties. This study aimed to investigate whether exogenous MSCs affect the function of club cells in an injured lung and whether these effects are related to the Notch signaling pathway. CCSP levels in bronchoalveolar lavage fluid (BALF) and serum were evaluated using enzyme-linked immunosorbent assay (ELISA) and the average fluorescence intensity (AFI) of CCSP in club cells was determined using flow cytometry. Immunohistochemistry and immunofluorescence were used to visualize club cells and proliferative club cells. The expression of important Notch signaling pathway components including Notchl~4, c-myc, Heyl and Hesl were also assessed. LY3039478 (LY), a specific inhibitor of the Notch signaling pathway, was applied. After MSCs intervention, CCSP levels decreased, and club cell AFI increased, indicating that the secretion of club cells had weakened. The expression of Notchl, Notch2, c-myc, Heyl, Hesl increased, accompanied by an increase in the number of proliferative club cells. Furthermore, MSCs enhanced the proliferation of club cells, while LY suppressed this phenomenon. In summary, MSCs reduced the secretion of club cells. And MSCs enhanced the proliferation of club cells partly via activating the Notch signaling pathway, which promoted lung injury repair.
机译:外源间充质干细胞(MSCs)通过细胞因子以及囊泡以及囊泡影响肺细胞并激活凹口信号传导途径,从而影响内源干细胞的增殖来修复受损组织。俱乐部细胞是内源性肺部干细胞,其增殖也与陷波信号通路密切相关。俱乐部细胞分泌蛋白(CCSP)具有抗炎和抗氧化性能。本研究旨在调查外源MSCs是否影响受伤肺中俱乐部细胞的功能,以及这些效果是否与陷波信号通路有关。使用酶联免疫吸附测定(ELISA)评估支气管肺泡灌洗液(BALF)和血清中的CCSP水平,并使用流式细胞仪测定CCSP中CCSP的平均荧光强度(AFI)。免疫组织化学和免疫荧光用于可视化俱乐部细胞和增殖俱乐部细胞。还评估了包括Notch1〜4,C-Myc,Heyl和Hesl的重要陷波信号通路组分的表达。 LY3039478(LY)是缺口信号通路的特异性抑制剂。在MSC干预后,CCSP水平降低,俱乐部细胞AFI增加,表明俱乐部细胞的分泌削弱了。 Notch1,Notch2,C-Myc,Heyl,Hesl的表达增加,伴随着增殖俱乐部细胞数量的增加。此外,MSCS增强了俱乐部细胞的增殖,而LY抑制了这种现象。总之,MSCS减少了俱乐部细胞的分泌。通过激活促进肺损伤修复的凹口信号通路,MSCs部分通过激活槽信号通路来增强俱乐部细胞的增强。

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