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人类滤泡树突状细胞表达CR1、CR2和CR3补体受体抗原。

Human follicular dendritic cells express CR1, CR2, and CR3 complement receptor antigens.

作者信息

Reynes M, Aubert J P, Cohen J H, Audouin J, Tricottet V, Diebold J, Kazatchkine M D

出版信息

J Immunol. 1985 Oct;135(4):2687-94.

PMID:2411809
Abstract

The expression of complement receptors by human follicular dendritic cells (FDC) was investigated by immunohistochemical techniques by using polyclonal and monoclonal antibodies to antigenic determinants of CR1, CR2, and CR3. Upon optical immunohistochemical examination of frozen sections from human reactive lymph nodes and tonsils by a three-step immunoperoxidase technique, a strong staining of cell bodies and cytoplasmic extensions of FDC was observed in germinal centers with anti-CR1 and anti-CR2 antibodies. Staining for these antigens was also found on cytoplasmic extensions of FDC in the mantle zone and on the plasma membrane of B cells in the entire follicles. Staining of FDC with anti-CR2 antibody was more intense than that of B lymphocytes. Monoclonal antibodies directed against epitopes of the alpha-chain of CR3 weakly stained FDC in follicles in a similar pattern to that which was observed on adjacent sections with mouse monoclonal antibody KIM4 that only recognizes FDC in human lymph nodes. Immunoelectron-microscopy was performed on frozen sections of a lymph node involved with a centroblastic centrocytic B malignant lymphoma and a reactive tonsil with the use of rabbit F(ab')2 anti-CR1 antibodies and mouse monoclonal anti-CR2 antibody. All the plasma membrane of the cell body and cytoplasmic extensions of FDC in germinal centers and in the mantle zones homogeneously stained for CR1 and CR2 antigens. Fibroblastic reticulum cells were negative. The plasma membrane of tumoral B lymphocytes strongly stained with anti-CR1 and weakly stained with anti-CR2 antibodies. The presence of CR1, CR2, and CR3 on FDC is a unique surface characteristic of these cells that should optimally allow the cells to bind antigen/antibody complexes bearing any type of C3 fragment.

摘要

利用针对CR1、CR2和CR3抗原决定簇的多克隆和单克隆抗体,通过免疫组织化学技术研究了人滤泡树突状细胞(FDC)补体受体的表达。采用三步免疫过氧化物酶技术对人反应性淋巴结和扁桃体的冰冻切片进行光学免疫组织化学检查时,在生发中心用抗CR1和抗CR2抗体观察到FDC的细胞体和细胞质突起有强烈染色。在套区FDC的细胞质突起以及整个滤泡中B细胞的质膜上也发现了这些抗原的染色。用抗CR2抗体对FDC的染色比B淋巴细胞更强。针对CR3α链表位的单克隆抗体以与仅识别人淋巴结中FDC的小鼠单克隆抗体KIM4在相邻切片上观察到的相似模式,对滤泡中的FDC进行弱染色。使用兔F(ab')2抗CR1抗体和小鼠单克隆抗CR2抗体,对1例中心母细胞-中心细胞性B恶性淋巴瘤累及的淋巴结和1个反应性扁桃体的冰冻切片进行免疫电子显微镜检查。生发中心和套区FDC的细胞体和细胞质突起的所有质膜均均匀地被CR1和CR2抗原染色。成纤维网状细胞为阴性。肿瘤性B淋巴细胞的质膜用抗CR1抗体染色强,用抗CR2抗体染色弱。FDC上CR1、CR2和CR3的存在是这些细胞独特的表面特征,这应能使这些细胞最佳地结合携带任何类型C3片段的抗原/抗体复合物。

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