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首页> 外文期刊>Biochemical and Biophysical Research Communications >TNF-α promotes human retinal pigment epithelial (RPE) cell migration by inducing matrix metallopeptidase 9 (MMP-9) expression through activation of Akt/mTORC1 signaling
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TNF-α promotes human retinal pigment epithelial (RPE) cell migration by inducing matrix metallopeptidase 9 (MMP-9) expression through activation of Akt/mTORC1 signaling

机译:通过激活AKT / MTORC1信号传导,通过诱导基质金属肽酶9(MMP-9)表达来促进人视网膜色素上皮(RPE)细胞迁移

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摘要

Tumor necrosis factor-alpha (TNF-α) promotes in vitro retinal pigment epithelial (RPE) cell migration to initiate proliferative vitreoretinopathy (PVR). Here we report that TNF-α promotes human RPE cell migration by inducing matrix metallopeptidase 9 (MMP-9) expression. Inhibition of MMP-9 by its inhibitor or its neutralizing antibody inhibited TNF-α-induced in vitro RPE cell migration. Reversely, exogenously-added active MMP-9 promoted RPE cell migration. Suppression Akt/mTOR complex 1(mTORC1) activation by LY 294002 and rapamycin inhibited TNF-α-mediated MMP-9 expression. To introduce a constitutively active Akt (CA-Akt) in cultured RPE cells increased MMP-9 expression, and to block mTORC1 activation by rapamycin inhibited its effect. RNA interference (RNAi)-mediated silencing of SIN1, a key component of mTOR complex 2 (mTORC2), had no effect on MMP-9 expression or secretion. In conclusion, this study suggest that TNF-α promotes RPE cell migration by inducing MMP-9 expression through activation of Akt/ mTORC1, but not mTORC2 signaling.
机译:肿瘤坏死因子-α(TNF-α)促进体外视网膜颜料上皮(RPE)细胞迁移以引发增殖性玻璃体病虫病(PVR)。在这里,我们认为TNF-α通过诱导基质金属肽酶9(MMP-9)表达来促进人RPE细胞迁移。其抑制剂或其中和抗体对MMP-9的抑制抑制TNF-α诱导的体外RPE细胞迁移。逆转,外源性添加的活性MMP-9促进了RPE细胞迁移。抑制AKT / MTOR复合物1(MTORC1)通过LY 294002激活和雷帕霉素抑制TNF-α介导的MMP-9表达。为了在培养的RPE细胞中引入组成型活性的AKT(CA-AKT)增加MMP-9表达,并阻止MTORC1通过雷帕霉素抑制其作用。 RNA干扰(RNAi)介导的SIN1的沉默,MTOR复合物2(MTORC2)的关键组分对MMP-9表达或分泌没有影响。总之,本研究表明TNF-α通过激活AKT / MTORC1而不是MTORC2信号传导来诱导MMP-9表达促进RPE细胞迁移。

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