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用胶体金偶联物对小鼠外周淋巴结高内皮细胞中L-选择素配体进行定位

Localization of ligands for L-selectin in mouse peripheral lymph node high endothelial cells by colloidal gold conjugates.

作者信息

Kikuta A, Rosen S D

机构信息

Department of Anatomy, Okayama University Medical School, Japan.

出版信息

Blood. 1994 Dec 1;84(11):3766-75.

PMID:7524748
Abstract

L-selectin, a Ca(2+)-dependent lectin-like receptor, mediates lymphocyte attachment to high endothelial venules (HEV) of peripheral lymph nodes (PLN) during the process of lymphocyte homing. Two endothelial-derived ligands for L-selectin, known as GlyCAM-1 (Sgp50) and CD34 (Sgp90), have been identified by affinity precipitation of lymph node extracts with a chimeric molecule that combines the extracellular domains of L-selectin with the human IgG1 Fc region (L-selectin-IgG) (J Cell Biol 110:2221, 1990). Here, using a histologic probe based on colloidal gold conjugated to L-selectin-IgG (LS-Ig), we performed morphologic mapping of the HEV ligands in PLN at both the light and electron microscopic levels. With a postembedding labeling method, intense LS-Ig-gold staining of PLN HEV was observed, while the HEV of Peyer's patches (PP) were negative. The specificity of LS-Ig-gold staining was established by pretreatment of sections with sialidase and coincubation of sections with EGTA, fucoidin, or L-selectin-IgG itself. In ultrastructural studies of high endothelial cells(HEC), gold particles were bound to the trans-Golgi network(TGN) and to peripheral vesicles in the cytoplasm. Gold labeling was also detected in a patchy distribution on the entire luminal vascular surface of HEC. Although the perivascular fibroreticular sheath of HEV was frequently labeled limited labeling was observed on the basolateral surfaces of the HEC. In most cases, the HEC membrane surrounding migrating lymphocytes was negative. These results show that L-selectin ligands pass through the Golgi apparatus during their biosynthesis, are stored in secretory granules, and are expressed on the vascular luminal surface of the HEC. A polyclonal antiserum to GlyCAM-1 intensely stained intracellular organelles in the biosynthetic pathway including cytoplasmic vesicles, but failed to stain the cell surface of HEC. Given its presence in serum as a soluble factor, GlyCAM-1 is likely to be a secretory product.

摘要

L-选择素是一种依赖钙离子的凝集素样受体,在淋巴细胞归巢过程中介导淋巴细胞与外周淋巴结(PLN)的高内皮微静脉(HEV)附着。通过用一种将L-选择素的细胞外结构域与人IgG1 Fc区结合的嵌合分子(L-选择素-IgG)对淋巴结提取物进行亲和沉淀,已鉴定出L-选择素的两种内皮细胞衍生配体,即GlyCAM-1(Sgp50)和CD34(Sgp90)(《细胞生物学杂志》110:2221,1990年)。在此,我们使用基于与L-选择素-IgG(LS-Ig)偶联的胶体金的组织学探针,在光学和电子显微镜水平上对PLN中HEV配体进行了形态学定位。采用包埋后标记法,观察到PLN的HEV有强烈的LS-Ig-金染色,而派伊尔结(PP)的HEV为阴性。通过用唾液酸酶预处理切片以及将切片与乙二醇双四乙酸(EGTA)、岩藻依聚糖或L-选择素-IgG本身共同孵育,确定了LS-Ig-金染色的特异性。在高内皮细胞(HEC)的超微结构研究中,金颗粒与反式高尔基体网络(TGN)以及细胞质中的外周囊泡结合。在HEC的整个管腔血管表面也检测到呈斑片状分布的金标记。尽管HEV的血管周围纤维网状鞘经常被标记,但在HEC的基底外侧表面观察到的标记有限。在大多数情况下,围绕迁移淋巴细胞的HEC膜为阴性。这些结果表明,L-选择素配体在生物合成过程中穿过高尔基体,储存于分泌颗粒中,并在HEC的血管腔表面表达。一种针对GlyCAM-1的多克隆抗血清强烈染色生物合成途径中的细胞内细胞器,包括细胞质囊泡,但未能染色HEC的细胞表面。鉴于其作为一种可溶性因子存在于血清中,GlyCAM-1可能是一种分泌产物。

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