细胞外基质金属蛋白酶诱导因子通过Toll样受体-4信号通路调节巨噬细胞自噬水平
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(1.联勤保障部队第920.医院心血管内科,昆明 650100;2. 江苏省苏州市第九人民医院心血管内科,江苏 苏州 215000)

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R543.5; R361.3

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国家自然科学基金(81370383)


Autophagy regulation by EMMPRIN in macrophages via Toll-like receptor-4 signaling pathway
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(1. Department of Cardiology, 920th Hospital of Joint Logistics Support Force, Kunming 650100, China;2. Department of Cardiology, Ninth People′s Hospital of Suzhou City, Suzhou 215000, Jiangsu Province, China)

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    摘要:

    目的 探讨细胞外基质金属蛋白酶诱导因子(EMMPRIN)是否通过Toll样受体-4(TLR4)通路调节巨噬细胞自噬水平。方法 用终浓度为5ng/ml的佛波酯(PMA)诱导人单核细胞白血病细胞系(THP-1)THP-1单核细胞48h,采用分化成功的巨噬细胞进行实验。实验分为空白对照组、EMMPRIN组和TAK-242组。蛋白印迹法检测各组TLR4、核因子-κB(NF-κB)、LC3-Ⅱ、Beclin1及P62蛋白表达水平;免疫荧光检测各组LC3-Ⅱ、Beclin1及P62蛋白荧光表达情况。采用SPSS 22.0软件对数据进行处理。结果 Western blot检测发现,EMMPRIN组与对照组及TAK-242组相比,TLR4、NF-κB蛋白表达水平均升高(均P<0.05),LC3-Ⅱ蛋白表达水平均升高(P<0.05),Beclin1蛋白表达水平也升高[EMMPRIN组与对照组比较,差异无统计学意义(P>0.05),但仍较对照组升高;EMMPRIN组与TAK-242组比较,差异有统计学意义(P<0.05)],P62蛋白表达水平均降低(均P<0.05)。免疫荧光检测发现,EMMPRIN组与对照组及TAK-242组相比,LC3-Ⅱ、Beclin1蛋白荧光表达水平明显升高(均P<0.05),P62蛋白表达水平无差异统计学意义(P>0.05)。结论 EMMPRI可能通过TLR4信号通路调节人THP-1巨噬细胞过度自噬。

    Abstract:

    Objective To investigate whether extracellular matrix metalloproteinase inducer (EMMPRIN) regulates autophagy in macrophages via the Toll-like receptor-4 (TLR4) pathway. Methods Human monocytic leukemia cell line (THP-1) monocytes were induced with phorbol ester (PMA) at a final concentration of 5 ng/ml for 48 h, and the successfully differentiated macrophages were tested. The cells were divided into the control group, EMMPRIN group and TAK-242 group. The expressions of TLR4, NF-κB, LC3-II, Beclin1 and P62 were detected by Western blot. The expressions of LC3-II, Beclin1 and P62 were detected by immunofluorescence. SPSS statistics 22.0 was used to process the data. Results Western blot showed that the EMMPRIN group had higher expression of TLR4, NF-κB, LC3-Ⅱ(P<0.05) than the control group and the TAK-242 group.Beclin1 protein expression level also increased in the EMMPRIN group, but with no significant difference compared with the control group (P>0.05), and with significant difference compared with the TAK-242 group(P<0.05). Expression of P62 were lower in the EMMPRIN group than the control group and the TAK-242 group(P<0.05). Expression of P62 were lower in the EMMPRIN group than the control group and the TAK-242 group (P<0.05). Immunofluorescence found that, the fluorescent expression of LC3-Ⅱ and Beclin1 protein were significantly higher in the EMMPRIN group than that in the control group and TAK-242 group (P<0.05), but the difference in the expression of P62 was not statistically significant. Conclusion EMMPRI may regulate excessive autophagy in human THP-1 macrophages through the TLR4 signaling pathway.

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赵嫦清,王志明,梁星,郭瑞威,杨丽霞,王先梅,石燕昆.细胞外基质金属蛋白酶诱导因子通过Toll样受体-4信号通路调节巨噬细胞自噬水平[J].中华老年多器官疾病杂志,2021,20(2):132~136

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  • 在线发布日期: 2021-03-01
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