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新型隐球菌感染脑微血管内皮细胞过程中人类CD44的作用。

Involvement of human CD44 during Cryptococcus neoformans infection of brain microvascular endothelial cells.

作者信息

Jong Ambrose, Wu Chun-Hua, Shackleford Gregory M, Kwon-Chung Kyung J, Chang Yun C, Chen Han-Min, Ouyang Yannan, Huang Sheng-He

机构信息

Division of Hematology-Oncology, The Saban Research Institute, Childrens Hospital Los Angeles, Department of Pediatrics, Keck School of Medicine, University of Southern California, Los Angeles, CA 90027, USA.

出版信息

Cell Microbiol. 2008 Jun;10(6):1313-26. doi: 10.1111/j.1462-5822.2008.01128.x. Epub 2008 Feb 4.

Abstract

Pathogenic yeast Cryptococcus neoformans causes devastating cryptococcal meningoencephalitis. Our previous studies demonstrated that C. neoformans hyaluronic acid was required for invasion into human brain microvascular endothelial cells (HBMEC), which constitute the blood-brain barrier. In this report, we demonstrate that C. neoformans hyaluronic acid interacts with CD44 on HBMEC. Our results suggest that HBMEC CD44 is a primary receptor during C. neoformans infection, based on the following observations. First, anti-CD44 neutralizing antibody treatment was able to significantly reduce C. neoformans association with HBMEC. Second, C. neoformans association was considerably impaired using either CD44-knock-down HBMEC or C. neoformans hyaluronic acid-deficient strains. Third, overexpression of CD44 in HBMEC increased their association activity towards C. neoformans. Fourth, confocal microscopic images showed that CD44 was enriched at and around the C. neoformans association sites. Fifth, upon C. neoformans and HBMEC engagement, a subpopulation of CD44 and actin translocated to the host membrane rafts. Our results highlight the interactions between C. neoformans hyaluronic acid and host CD44 and the dynamic results of these interactions, which may represent events during the adhesion and entry of C. neoformans at HBMEC membrane rafts.

摘要

致病性酵母新型隐球菌可引发毁灭性的隐球菌性脑膜脑炎。我们之前的研究表明,新型隐球菌的透明质酸是其侵入构成血脑屏障的人脑微血管内皮细胞(HBMEC)所必需的。在本报告中,我们证明新型隐球菌的透明质酸与HBMEC上的CD44相互作用。基于以下观察结果,我们的研究结果表明HBMEC CD44是新型隐球菌感染过程中的主要受体。首先,抗CD44中和抗体处理能够显著降低新型隐球菌与HBMEC的结合。其次,使用CD44敲低的HBMEC或新型隐球菌透明质酸缺陷菌株时,新型隐球菌的结合能力会受到显著损害。第三,HBMEC中CD44的过表达增加了它们对新型隐球菌的结合活性。第四,共聚焦显微镜图像显示CD44在新型隐球菌结合位点及其周围富集。第五,新型隐球菌与HBMEC接触后,一部分CD44和肌动蛋白会转移到宿主细胞膜筏上。我们的研究结果突出了新型隐球菌透明质酸与宿主CD44之间的相互作用以及这些相互作用的动态结果,这可能代表了新型隐球菌在HBMEC膜筏上黏附和进入过程中的事件。

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