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脂多糖和肽聚糖在人外周血单核细胞上共享结合位点。

Lipopolysaccharide and peptidoglycan share binding sites on human peripheral blood monocytes.

作者信息

Rabin R L, Bieber M M, Teng N N

机构信息

Department of Gynecology and Obstetrics, Stanford University School of Medicine, California.

出版信息

J Infect Dis. 1993 Jul;168(1):135-42. doi: 10.1093/infdis/168.1.135.

Abstract

p73, a binding site for lipopolysaccharide (LPS) on human peripheral blood monocytes was identified using the radiolabeled photoaffinity cross-linker sulfosuccinimidyl 2-(p-azidosalicylamido)ethyl-1,3'-dithiopropionate (SASD). The 125I-labeled conjugate of SASD and LPS (125I-labeled ASD-LPS) was bound to monocytes and UV cross-linked, and the cellular extracts were analyzed with two-dimensional SDS-PAGE and autoradiography. In addition to the major binding site on human monocytes at 73 kDa, isoelectric point 5.95, there were multiple minor binding sites that recognized both smooth and rough LPS. Binding of 125I-labeled ASD-LPS to monocytes is concentration dependent, decreased in the absence of calcium and magnesium, and inhibited by either excess LPS or the low-molecular-weight soluble isolate of bacterial cell wall peptidoglycan (sPGN). However, sPGN only minimally stimulates tumor necrosis factor (TNF) secretion by human peripheral blood mononuclear cells. In contrast, the relatively insoluble high-molecular-weight peptidoglycan significantly stimulates TNF secretion.

摘要

利用放射性标记的光亲和交联剂磺基琥珀酰亚胺2-(对叠氮水杨酰胺基)乙基-1,3'-二硫代丙酸酯(SASD),确定了人外周血单核细胞上脂多糖(LPS)的一个结合位点。将SASD与LPS的125I标记共轭物(125I标记的ASD-LPS)与单核细胞结合并进行紫外线交联,然后用二维SDS-PAGE和放射自显影分析细胞提取物。除了在人单核细胞上位于73 kDa、等电点5.95处的主要结合位点外,还有多个次要结合位点,这些位点能识别光滑型和粗糙型LPS。125I标记的ASD-LPS与单核细胞的结合具有浓度依赖性,在无钙和镁的情况下会降低,并且会被过量的LPS或细菌细胞壁肽聚糖的低分子量可溶性分离物(sPGN)抑制。然而,sPGN仅能轻微刺激人外周血单核细胞分泌肿瘤坏死因子(TNF)。相比之下,相对不溶性的高分子量肽聚糖能显著刺激TNF分泌。

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