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非受体酪氨酸激酶Tec控制非经典半胱天冬酶-8炎性小体的组装和活性。

The non-receptor tyrosine kinase Tec controls assembly and activity of the noncanonical caspase-8 inflammasome.

作者信息

Zwolanek Florian, Riedelberger Michael, Stolz Valentina, Jenull Sabrina, Istel Fabian, Köprülü Afitap Derya, Ellmeier Wilfried, Kuchler Karl

机构信息

Department of Molecular Genetics, Medical University of Vienna, Max F. Perutz Laboratories, Vienna, Austria.

Division of Immunobiology, Institute of Immunology, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.

出版信息

PLoS Pathog. 2014 Dec 4;10(12):e1004525. doi: 10.1371/journal.ppat.1004525. eCollection 2014 Dec.

Abstract

Tec family kinases are intracellular non-receptor tyrosine kinases implicated in numerous functions, including T cell and B cell regulation. However, a role in microbial pathogenesis has not been described. Here, we identified Tec kinase as a novel key mediator of the inflammatory immune response in macrophages invaded by the human fungal pathogen C. albicans. Tec is required for both activation and assembly of the noncanonical caspase-8, but not of the caspase-1 inflammasome, during infections with fungal but not bacterial pathogens, triggering the antifungal response through IL-1β. Furthermore, we identify dectin-1 as the pathogen recognition receptor being required for Syk-dependent Tec activation. Hence, Tec is a novel innate-specific inflammatory kinase, whose genetic ablation or inhibition by small molecule drugs strongly protects mice from fungal sepsis. These data demonstrate a therapeutic potential for Tec kinase inhibition to combat invasive microbial infections by attenuating the host inflammatory response.

摘要

Tec家族激酶是细胞内非受体酪氨酸激酶,参与多种功能,包括T细胞和B细胞调节。然而,其在微生物致病机制中的作用尚未见报道。在此,我们确定Tec激酶是被人类真菌病原体白色念珠菌侵袭的巨噬细胞中炎症免疫反应的一种新型关键介质。在真菌感染而非细菌感染过程中,Tec是激活和组装非经典caspase-8所必需的,但不是caspase-1炎性小体所必需的,它通过IL-1β触发抗真菌反应。此外,我们确定dectin-1是Syk依赖性Tec激活所必需的病原体识别受体。因此,Tec是一种新型的固有特异性炎症激酶,其基因敲除或小分子药物抑制可强烈保护小鼠免受真菌败血症。这些数据表明,抑制Tec激酶以减轻宿主炎症反应,对于对抗侵袭性微生物感染具有治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f3f/4256681/5029b4e0f324/ppat.1004525.g001.jpg

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