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新型隐球菌荚膜基质中补体成分3的差异定位

Differential localization of complement component 3 within the capsular matrix of Cryptococcus neoformans.

作者信息

Gates Marcellene A, Kozel Thomas R

机构信息

Department of Microbiology and Immunology/320, University of Nevada School of Medicine, Reno, NV 89557, USA.

出版信息

Infect Immun. 2006 Jun;74(6):3096-106. doi: 10.1128/IAI.01213-05.

Abstract

The polysaccharide capsule of Cryptococcus neoformans is a powerful activator of the complement system. The goal of the present study was to assess serum and cellular variables that influence the sites for C3 binding within the capsular matrix. Confocal microscopy using fluorophore-labeled polyclonal anti-C3 and anticapsular monoclonal antibodies and rosetting of fluorescent microspheres coated with anti-C3 were used to identify sites of C3 binding relative to the capsular edge. The results showed that the source of serum was a major variable influencing localization of C3. C3 bound at or very near the capsular edge in the case of human serum. C3 deposition was further from the capsule edge with guinea pig and rat sera; in the case of mouse serum, there was no binding of C3 in the outer region of the capsule. Addition of human C3 to mouse serum led to deposition of the C3 at the capsular edge, indicating that distinct properties of mouse and human C3 account for the differential localization of C3. Finally, the density of the capsular matrix was an important variable in determining sites for C3 deposition. Yeast cells with a high concentration of polysaccharide near the capsule edge supported deposition of mouse C3 at or near the capsular edge, whereas cells with a low matrix density showed deposition well beneath the edge. Taken together, these results indicate that the spatial deposition of C3 within the capsular matrix is a complex process that is influenced by the serum source and the density of the capsular matrix.

摘要

新型隐球菌的多糖荚膜是补体系统的强力激活剂。本研究的目的是评估影响补体C3在荚膜基质内结合位点的血清和细胞变量。使用荧光团标记的多克隆抗C3和抗荚膜单克隆抗体进行共聚焦显微镜检查,以及用抗C3包被的荧光微球进行花环试验,以确定相对于荚膜边缘的C3结合位点。结果表明,血清来源是影响C3定位的主要变量。在人血清的情况下,C3在荚膜边缘或非常靠近荚膜边缘处结合。豚鼠和大鼠血清中的C3沉积距离荚膜边缘更远;在小鼠血清的情况下,在荚膜的外部区域没有C3结合。向小鼠血清中添加人C3导致C3在荚膜边缘沉积,表明小鼠和人C3的不同特性导致了C3的差异定位。最后,荚膜基质的密度是决定C3沉积位点的重要变量。在荚膜边缘附近多糖浓度高的酵母细胞支持小鼠C3在荚膜边缘或其附近沉积,而基质密度低的细胞则在边缘下方很远的位置出现沉积。综上所述,这些结果表明C3在荚膜基质内的空间沉积是一个复杂的过程,受血清来源和荚膜基质密度的影响。

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本文引用的文献

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Molecular architecture of the Cryptococcus neoformans capsule.新型隐球菌荚膜的分子结构
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