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致病性奈瑟菌IV型菌毛介导的细胞信号传导

Cell signaling by the type IV pili of pathogenic Neisseria.

作者信息

Källström H, Islam M S, Berggren P O, Jonsson A B

机构信息

Microbiology and Tumorbiology Center, Karolinska Institute, S-171 77, Stockholm, Sweden.

出版信息

J Biol Chem. 1998 Aug 21;273(34):21777-82. doi: 10.1074/jbc.273.34.21777.

Abstract

Neisseria gonorrhoeae and Neisseria meningitidis are Gram-negative bacterial pathogens that infect human mucosal epithelia. Type IV pilus-mediated adherence of these bacteria is a crucial early event for establishment of infection. In this work, we show that the type IV pili transduce a signal into the eucaryotic host cell. Purified adherent pili, but not pili from a low binding mutant, trigger an increase in the cytosolic free calcium ([Ca2+]i) in target epithelial cells, a signal known to control many cellular responses. The [Ca2+]i increase was blocked by antibodies against CD46, a putative pilus receptor, suggesting a role for this protein in signal transduction. Pilus-mediated attachment was inhibited by depletion of host cell intracellular Ca2+ stores but not by removal of extracellular Ca2+. Further, kinase inhibition studies showed that pilus-mediated adherence is dependent on casein kinase II. In summary, these data reveal a novel function of the type IV pili, namely induction of signal transduction pathways in host cells.

摘要

淋病奈瑟菌和脑膜炎奈瑟菌是感染人类黏膜上皮的革兰氏阴性细菌病原体。这些细菌通过IV型菌毛介导的黏附是感染建立的关键早期事件。在这项研究中,我们表明IV型菌毛将信号传导至真核宿主细胞。纯化的黏附菌毛,而非低结合突变体的菌毛,会引发靶上皮细胞胞质游离钙([Ca2+]i)增加,这是一种已知可控制多种细胞反应的信号。抗CD46(一种假定的菌毛受体)抗体可阻断[Ca2+]i增加,表明该蛋白在信号转导中起作用。宿主细胞内钙库耗竭可抑制菌毛介导的附着,但去除细胞外钙则无此作用。此外,激酶抑制研究表明菌毛介导的黏附依赖于酪蛋白激酶II。总之,这些数据揭示了IV型菌毛的一种新功能,即在宿主细胞中诱导信号转导途径。

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