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来自四名完全或部分白细胞黏附分子缺乏症患者的白细胞含有共同的β亚基前体和β亚基信使核糖核酸。

Leukocytes from four patients with complete or partial Leu-CAM deficiency contain the common beta-subunit precursor and beta-subunit messenger RNA.

作者信息

Dana N, Clayton L K, Tennen D G, Pierce M W, Lachmann P J, Law S A, Arnaout M A

出版信息

J Clin Invest. 1987 Mar;79(3):1010-5. doi: 10.1172/JCI112868.

Abstract

Deficiency of a family of three leukocyte adhesion molecules (Leu-CAM) is associated with recurrent and life-threatening bacterial infections in man. Each of the three antigens, Mo1, LFA-1, and Leu M5 has a distinct alpha subunit noncovalently associated with a common beta subunit that appears to be required for the expression of these antigens on the cell surface. To investigate the molecular basis of Leu-CAM deficiency, we studied leukocytes from four unrelated patients suffering from complete or partial Leu-CAM deficiency using immunoprecipitation of metabolically labeled proteins, RNA extraction, and Northern blot analysis. We found that B cells from all four patients synthesized a normal sized beta subunit precursor that either failed to "mature" or matured only partially to the membrane expressed form. B cells from all four patients also had a single normal sized beta subunit mRNA of approximately 3.4 kb. Leu-CAM deficiency, in these unrelated patients, is not due to the absence of the beta chain gene or to aberrant splicing of its mRNA and are consistent with a defective beta subunit gene resulting in abnormal posttranslational processing of the synthesized molecule.

摘要

三种白细胞黏附分子(Leu-CAM)家族的缺陷与人反复发生的、危及生命的细菌感染相关。三种抗原Mo1、淋巴细胞功能相关抗原-1(LFA-1)和Leu M5中的每一种都有一个独特的α亚基,该亚基与一个共同的β亚基非共价结合,而这个共同的β亚基似乎是这些抗原在细胞表面表达所必需的。为了研究Leu-CAM缺陷的分子基础,我们使用代谢标记蛋白的免疫沉淀、RNA提取和Northern印迹分析,对四名患有完全或部分Leu-CAM缺陷的无关患者的白细胞进行了研究。我们发现,所有四名患者的B细胞都合成了正常大小的β亚基前体,该前体要么未能“成熟”,要么仅部分成熟为膜表达形式。所有四名患者的B细胞也都有一条约3.4 kb的正常大小的β亚基mRNA。在这些无关患者中,Leu-CAM缺陷并非由于β链基因缺失或其mRNA的异常剪接,而是与β亚基基因缺陷导致合成分子的翻译后加工异常一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed8a/424264/842533a625a6/jcinvest00114-0351-a.jpg

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