[青碱通过阻断大鼠miR-21/ADAMTS-1信号通路改善博来霉素a5诱导的肺纤维化]。

Lijing Liu, Hong Qian, Qingxin Meng, Xiang Zhang, Yingmin Wei, Jianbin He
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Thirty SD rats were randomly divided into control group, sinomenine group and sinomenine combined with miR-21 agomir group, with 10 animals in each group. Bleomycin A5 were intratracheally administered to establish the PF model. Then, rats in control group, sinomenine group and sinomenine +miR-21 agomir group were treated with 9 g/L sodium chloride solution, sinomenine and sinomenine+miR-21 agomir, respectively. On day 28, all rats were sacrificed. HE and Masson staining was performed in pulmonary tissue. The expression of ADAMTS-1, Col1 and Col3 in pulmonary tissue were detected by qRT-PCR and/or Western blot analysis. ELISA was used to measure serum procollagen type 1 carboxyterminal propeptide (P1CP) and procollagen type 3 aminoterminal propeptide (P3NP) levels. Results Administration of sinomenine decreased miR-21 levels, up-regulated ADAMTS-1 expression, and promoted Col1 and Col3 degradation in MRC-5 cells. 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引用次数: 0

摘要

目的探讨青藤碱对博来霉素a5诱导大鼠肺纤维化的影响及其机制。方法用青藤碱培养MRC-5细胞,MTT法确定青藤碱的最佳浓度和作用时间。随后,将MRC-5细胞与80 μmol/L青藤碱孵育48小时,或在青藤碱处理前转染miR-21 mimic/a分解素样酶和带有血栓反应蛋白1型基序(ADAMTS-1) siRNA的金属蛋白酶。通过实时荧光定量PCR (qRT-PCR)和/或Western blot分析检测miR-21、ADAMTS-1、1型胶原(Col1)和3型胶原(Col3)的表达。将30只SD大鼠随机分为对照组、青藤碱组和青藤碱联合miR-21 agomir组,每组10只。经气管给药博莱霉素A5建立PF模型。对照组、青藤碱组、青藤碱+miR-21 agomir组大鼠分别给予9 g/L氯化钠溶液、青藤碱、青藤碱+miR-21 agomir。第28天处死所有大鼠。肺组织行HE、Masson染色。采用qRT-PCR和/或Western blot检测肺组织中ADAMTS-1、Col1和Col3的表达。ELISA法检测血清前胶原1型羧基末端前肽(P1CP)和前胶原3型氨基末端前肽(P3NP)水平。结果青叶碱降低MRC-5细胞中miR-21水平,上调ADAMTS-1表达,促进Col1和Col3降解。重要的是,干扰miR-21/ADAMTS-1信号通路部分逆转了青碱对Col1和Col3降解的促进作用。青叶碱治疗SD大鼠可降低肺泡炎和PF评分,降低血清P1CP和P3NP水平,上调肺ADAMTS-1表达,下调Col1和Col3表达。然而,这些作用被mir - 21agomir逆转。结论青叶碱通过miR-21/ADAMTS-1通路促进大鼠Col1和Col3降解,抑制PF。
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[Sinomenine ameliorates bleomycin A5-induced pulmonary fibrosis by blocking the miR-21/ADAMTS-1 signaling pathway in rats].

Objective To explore the impact of sinomenine on bleomycin A5-induced pulmonary fibrosis (PF) in rats and the underlying mechanism. Methods MRC-5 cells were cultured and treated with sinomenine to determine its optimal concentration and time through the MTT assay. Subsequently, MRC-5 cells were incubated with 80 μmol/L sinomenine for 48 hours or transfected with miR-21 mimic/a disintegrin-like and metalloproteinase with thrombospondin type 1 motif (ADAMTS-1) siRNA prior to sinomenine treatment. The expression of miR-21, ADAMTS-1, collagen type 1 (Col1) and collagen type 3 (Col3) was detected by quantitative real-time PCR (qRT-PCR) and/or Western blot analysis. Thirty SD rats were randomly divided into control group, sinomenine group and sinomenine combined with miR-21 agomir group, with 10 animals in each group. Bleomycin A5 were intratracheally administered to establish the PF model. Then, rats in control group, sinomenine group and sinomenine +miR-21 agomir group were treated with 9 g/L sodium chloride solution, sinomenine and sinomenine+miR-21 agomir, respectively. On day 28, all rats were sacrificed. HE and Masson staining was performed in pulmonary tissue. The expression of ADAMTS-1, Col1 and Col3 in pulmonary tissue were detected by qRT-PCR and/or Western blot analysis. ELISA was used to measure serum procollagen type 1 carboxyterminal propeptide (P1CP) and procollagen type 3 aminoterminal propeptide (P3NP) levels. Results Administration of sinomenine decreased miR-21 levels, up-regulated ADAMTS-1 expression, and promoted Col1 and Col3 degradation in MRC-5 cells. Importantly, interfering with the miR-21/ADAMTS-1 signaling pathway partially reversed the promotive effect of sinomenine on Col1 and Col3 degradation. Treatment of SD rats with sinomenine reduced alveolitis and PF scores, decreased serum P1CP and P3NP levels, up-regulated pulmonary ADAMTS-1 expression, and down-regulated Col1 and Col3 expression. However, these effects were reversed by miR-21 agomir. Conclusion Sinomenine promotes Col1 and Col3 degradation and inhibits PF in rats by miR-21/ADAMTS-1 pathway.

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[miR-18a ameliorates inflammation and tissue injury in a mouse model of allergic rhinitis via blocking TLR4/NF-κB pathway]. [The number of TIGIT+CD8+ T cells increases but their cytokine secretion decreases in the lungs of Plasmodium yoelii infected mice]. [The mechanism of microcystin leucine-arginine (MC-LR)-induced injury of Sertoli cell immune response and biological behavior]. [IgG Fc binding protein (FCGBP) as a prognostic marker of low-grade glioma and its correlation analysis with immune infiltration]. [Sinomenine ameliorates bleomycin A5-induced pulmonary fibrosis by blocking the miR-21/ADAMTS-1 signaling pathway in rats].
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