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用单克隆抗体R2D6鉴定的大鼠胰腺β细胞表面的一种神经节苷脂抗原。

A ganglioside antigen on the rat pancreatic B cell surface identified by monoclonal antibody R2D6.

作者信息

Alejandro R, Shienvold F L, Hajek S A, Pierce M, Paul R, Mintz D H

出版信息

J Clin Invest. 1984 Jul;74(1):25-38. doi: 10.1172/JCI111409.

Abstract

In an attempt to identify B cell specific antigens, we have generated a mouse monoclonal antibody, R2D6, which is directed against plasma membranes of rat pancreatic B cells but against no other pancreatic cells. R2D6 crossreacted with mouse and guinea pig B cells, but not with human or dog. The B cell specificity of R2D6 was utilized in fluorescence-activated cell sorting to prepare highly enriched separate populations of viable pancreatic islet B cells and A cells. R2D6 also recognized adrenal chromaffin cells, secretory cells in the anterior pituitary, and the myenteric plexus of the gastrointestinal tract. Trypsin, chymotrypsin, papain, ficin, and pronase had no effect on R2D6-binding to dissociated rat islet cells. However, neuraminidase treatment of intact cells reduced R2D6-binding by 75%. The antigen recognized by R2D6, Ag(R2D6), could be quantitatively extracted from rat islets by dichloromethane/methanol (2:1) and, after drying, was soluble in methanol alone as well as in phosphate-buffered saline. When the dichloromethane/methanol extract (DME) was bound to polyvinylchloride microtiter plates, antigenic activity was retained and remained insensitive to pronase. In this solvent-extracted form, antigenic activity was totally destroyed by neuraminidase. Therefore, sialic acid is either an integral part of, or is related sterically to the binding site (epitope) for R2D6. In high performance thin-layer chromatographs of the DME, developed in 60:40:9 chloroform/methanol/2.5 N ammonia, Ag(R2D6) migrated with a relative mobility (Rf) of 0.54 +/- 0.07 (n = 3), which was a position nearly coincident with the purified brain ganglioside, GD1a. The antigen bound to DEAE-Sephacel, was not inactivated by mild treatment with base (which hydrolyzes phospholipids) and eluted in ganglioside fractions upon C18 Sep-Pak and upon silicic acid chromatography. Hence, the solubility characteristics, enzyme sensitivities, and behavior of Ag(R2D6) in four chromatography systems are consistent with its identification as a ganglioside.

摘要

为了鉴定B细胞特异性抗原,我们制备了一种小鼠单克隆抗体R2D6,它针对大鼠胰腺B 细胞的质膜,但不针对其他胰腺细胞。R2D6与小鼠和豚鼠的B细胞发生交叉反应,但不与人或狗的B细胞反应。利用R2D6的B细胞特异性,通过荧光激活细胞分选技术制备了高纯度的、存活的胰腺胰岛B细胞和A细胞分离群体。R2D6还识别肾上腺嗜铬细胞、垂体前叶的分泌细胞以及胃肠道的肌间神经丛。胰蛋白酶、糜蛋白酶、木瓜蛋白酶、无花果蛋白酶和链霉蛋白酶对R2D6与解离的大鼠胰岛细胞的结合没有影响。然而,用神经氨酸酶处理完整细胞可使R2D6的结合减少75%。R2D6识别的抗原Ag(R2D6) 可用二氯甲烷/甲醇(2:1)从大鼠胰岛中定量提取,干燥后,它可溶于单独的甲醇以及磷酸盐缓冲盐水中。当二氯甲烷/甲醇提取物(DME)与聚氯乙烯微量滴定板结合时,抗原活性得以保留,并且对链霉蛋白酶不敏感。以这种溶剂提取形式存在的抗原活性被神经氨酸酶完全破坏。因此,唾液酸要么是R2D6结合位点(表位)的组成部分,要么在空间上与之相关。在以60:40:9氯仿/甲醇/2.5N氨展开的DME高效薄层色谱中,Ag(R2D6) 的相对迁移率(Rf)为0.54±0.07(n = 3),这一位置与纯化的脑苷脂GD1a几乎一致。与DEAE-琼脂糖凝胶结合的抗原,在温和的碱处理(水解磷脂)下不会失活,并且在C18 Sep-Pak和硅酸色谱上洗脱于神经节苷脂部分。因此,Ag(R2D6) 在四种色谱系统中的溶解性特征、酶敏感性和行为与其被鉴定为神经节苷脂一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f062/425181/f5adac217054/jcinvest00134-0038-a.jpg

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