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Mitogen-activated protein kinases are required for effective infection of human choroid plexus epithelial cells by Listeria monocytogenes

机译:促丝糖型活化的蛋白激酶是通过李斯特菌单核细胞生成的人脉络膜上皮细胞有效感染

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Listeria monocytogenes, a Gram-positive bacterium, can cause meningitis after invading the human central nervous system. The blood cerebrospinal fluid barrier (BCSFB), located at the epithelium of the choroid plexus, is a possible entry site for L. monocytogenes into the brain, and in vitro L. monocytogenes invades human choroid plexus epithelial papilloma (HIBCPP) cells. Although host cell signal transduction subsequent to infection by L. monocytogenes has been investigated, the role of mitogen-activated protein kinases (MAPK) is not clarified yet. We show that infection with L. monocytogenes causes activation of the MAPKs Erk1/2 and p38 preferentially when bacteria are added to the physiologically more relevant basolateral side of HIBCPP cells. Deletion of the listerial,virulence factors Internalin (In1A) and In1B reduces MAPK activation. Whereas inhibition of either Erk1/2 or p38 signaling significantly attenuates infection of HIBCPP cells with L. monocytogenes, simultaneous inhibition of both MAPK pathways shows an additive effect, and Erk1/2 and p38 are involved in regulation of cytokine and chemokine expression following infection. Blocking of endocytosis with the synthetic dynamin inhibitor dynasore strongly abrogates infection of HIBCPP cells with L. monocytogenes. Concurrent inhibition of MAPK signaling further reduces infection, suggesting MAPKs mediate infection with L. monocytogenes during inhibition of dynamin-mediated endocytosis. (C) 2016 Institut Pasteur. Published by Elsevier Masson SAS. All rights reserved.
机译:Listeria单核细胞增生,革兰氏阳性细菌,可在侵入人的中枢神经系统后引起脑膜炎。位于脉络膜上皮的血液脑脊液屏障(BCSFB)是L.单核细胞生入大脑的可能进入部位,并且在体外L.单核细胞生成单核细胞生成的人脉络膜上皮乳头瘤(HiBCPP)细胞。尽管已经研究了L.单核细胞增生后感染后的宿主细胞信号转导,但尚未澄清丝裂剂活化的蛋白激酶(MAPK)的作用。我们表明,当将细菌添加到HiBCPP细胞的生理学更相关的基石外侧时,对L.单核细胞增生的感染导致MAPKS ERK1 / 2和P38的激活。删除Listerial,毒力因子内部(In1a)和In1b减少MAPK激活。然而,ERK1 / 2或P38信号传导的抑制显着衰减了用L.单核细胞生成的HiBCPP细胞感染,同时抑制MAPK途径显示添加效果,并且ERK1 / 2和P38参与感染后细胞因子和趋化因子表达的调节。用合成发电机抑制剂Dynasore阻断内吞作用症强烈消除了L.单核细胞增生的Hibcpp细胞感染。 MAPK信号的同时抑制进一步减少了感染,暗示在抑制发电机介导的内吞作用期间用L.单核细胞生成的MApks调节感染。 (c)2016 Institut Pasteur。由Elsevier Masson SA出版。版权所有。

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