首页> 外文期刊>Rheumatology >Cyclophilin A up-regulates MMP-9 expression and adhesion of monocytes/macrophages via CD147 signalling pathway in rheumatoid arthritis.
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Cyclophilin A up-regulates MMP-9 expression and adhesion of monocytes/macrophages via CD147 signalling pathway in rheumatoid arthritis.

机译:亲环蛋白A通过类风湿关节炎中的CD147信号通路上调MMP-9表达和单核细胞/巨噬细胞的粘附。

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OBJECTIVES: To investigate whether cyclophilin A (CypA) can up-regulate the expression of MMP-2 and MMP-9 in monocytes/macrophages and whether CD147 facilitates this regulation in RA. Methods. Peripheral blood monocytes were isolated from RA patients and differentiated into macrophages by M-CSF (15 ng/ml). Under CypA stimulation (200 ng/ml), the protein release and activation of MMPs were detected by gelatin zymography and invasion assay. Human monocyte cell line THP-1 cells were selected for the advanced searching for potential interaction between CypA and CD147 in production of MMPs and cell adhesion to extracellular matrix (ECM). RESULTS: CypA significantly increased production and activation of MMP-9, not MMP-2, in the monocytes/macrophages derived from RA SF. CSA and HAb18G/CD147 antagonistic peptide AP-9 against CD147, respectively, dramatically decreased MMP-2 and MMP-9 expression, both in the absence or presence of CypA. Similar effects of CypA on MMP-9 production and cell invasion were observed in THP-1 cells. CypA-induced nuclear factor kappaB (NF-kappaB) activity for MMP-9 transcription were strongly blocked by extracellular signal-regulated kinase (ERK), c-Jun amino terminal kinase (JNK) inhibitors (U0126 and SP600125, respectively), but not by p38 mitogen-activated protein kinase (MAPK) inhibitors (SB203580). CypA also induced calcium mobilization and increased the adhesion of THP-1 cells to ECM. CONCLUSIONS: These findings suggest that in RA, the abundant CypA, by its direct binding to CD147, up-regulates MMP-9 expression and adhesion of monocytes/macrophages to ECM, and the cyclophilin-CD147 interactions might contribute to the destruction of cartilage and bone.
机译:目的:探讨亲环蛋白A(CypA)是否可以上调单核细胞/巨噬细胞中MMP-2和MMP-9的表达,以及CD147是否促进RA中的这种调节。方法。从RA患者中分离出外周血单核细胞,并通过M-CSF(15 ng / ml)分化为巨噬细胞。在CypA刺激下(200 ng / ml),通过明胶酶谱和侵袭试验检测了蛋白的释放和MMP的活化。选择人类单核细胞系THP-1细胞进行高级搜索,以寻找CypA和CD147之间产生MMP以及细胞粘附至细胞外基质(ECM)的潜在相互作用。结果:CypA显着增加了源自RA SF的单核细胞/巨噬细胞中MMP-9(而非MMP-2)的产生和激活。在不存在或存在CypA的情况下,分别针对CD147的CSA和HAb18G / CD147拮抗肽AP-9显着降低了MMP-2和MMP-9的表达。在THP-1细胞中观察到了CypA对MMP-9产生和细胞侵袭的类似作用。 CypA诱导的MMP-9转录的核因子kappaB(NF-kappaB)活性被细胞外信号调节激酶(ERK),c-Jun氨基末端激酶(JNK)抑制剂(分别为U0126和SP600125)强烈阻断,但没有通过p38丝裂原活化蛋白激酶(MAPK)抑制剂(SB203580)。 CypA还诱导钙动员,并增加THP-1细胞与ECM的粘附。结论:这些发现表明,在RA中,丰富的CypA通过直接与CD147结合,上调MMP-9的表达和单核细胞/巨噬细胞对ECM的粘附,亲环蛋白-CD147的相互作用可能有助于破坏软骨和骨。

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