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新型隐球菌荚膜启动替代补体途径激活的早期事件。

Early events in initiation of alternative complement pathway activation by the capsule of Cryptococcus neoformans.

作者信息

Kozel T R, Wilson M A, Murphy J W

机构信息

Department of Microbiology, University of Nevada, Reno 89557.

出版信息

Infect Immun. 1991 Sep;59(9):3101-10. doi: 10.1128/iai.59.9.3101-3110.1991.

Abstract

The capsule of Cryptococcus neoformans is a powerful activator of the alternative complement pathway. This study examined the manner in which the cryptococcal capsule influences initiation of and early events in complement activation by C. neoformans. These studies examined the effects of the classical and alternative pathways on the kinetics and early sites for deposition of C3 fragments on encapsulated cryptococci, nonencapsulated cryptococci, and zymosan. The results showed that nonencapsulated cryptococci and zymosan are qualitatively and quantitatively similar in the manner in which they initiate complement activation. Both utilize the classical and alternative pathways. Initiation via the classical pathway occurs suddenly and simultaneously at sites distributed over the entire cell surface. Initiation of the alternative pathway by zymosan and nonencapsulated cryptococci is characterized by a lag of 6 to 8 min before appreciable amounts of C3 accumulate on the cells. Alternative pathway initiation by zymosan and nonencapsulated cryptococci occurs at a limited number of focal initiation sites that expand with alternative pathway amplification to cover the cell surface. Presence of the cryptococcal capsule blocks classical pathway initiation, which would normally occur at the cryptococcal cell wall, and produces an initiation that is dependent solely on the alternative pathway. Initiation of the alternative pathway by the cryptococcal capsule is characterized by a lag in C3 accumulation and the appearance of a limited number of focal initiation sites which resemble those observed when the alternative pathway is activated by zymosan and nonencapsulated cryptococci.

摘要

新型隐球菌的荚膜是替代补体途径的强力激活剂。本研究探讨了隐球菌荚膜影响新型隐球菌补体激活起始及早期事件的方式。这些研究考察了经典途径和替代途径对C3片段在被包囊的隐球菌、无荚膜隐球菌和酵母聚糖上沉积的动力学及早期位点的影响。结果显示,无荚膜隐球菌和酵母聚糖在启动补体激活的方式上在定性和定量方面相似。二者均利用经典途径和替代途径。通过经典途径启动补体激活在整个细胞表面分布的位点突然且同时发生。酵母聚糖和无荚膜隐球菌通过替代途径启动补体激活的特征是,在相当数量的C3在细胞上积累之前有6至8分钟的延迟。酵母聚糖和无荚膜隐球菌通过替代途径启动补体激活发生在有限数量的局灶性起始位点,这些位点随着替代途径的放大而扩展以覆盖细胞表面。隐球菌荚膜的存在会阻断通常在隐球菌细胞壁发生的经典途径启动,并产生仅依赖替代途径的启动。隐球菌荚膜通过替代途径启动补体激活的特征是C3积累有延迟以及出现有限数量的局灶性起始位点,这些位点类似于酵母聚糖和无荚膜隐球菌激活替代途径时所观察到的位点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e956/258140/035e216c1993/iai00045-0260-a.jpg

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