Dana N, Clayton L K, Tennen D G, Pierce M W, Lachmann P J, Law S A, Arnaout M A
J Clin Invest. 1987 Mar;79(3):1010-5. doi: 10.1172/JCI112868.
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.
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。