Berman C L, Yeo E L, Wencel-Drake J D, Furie B C, Ginsberg M H, Furie B
J Clin Invest. 1986 Jul;78(1):130-7. doi: 10.1172/JCI112542.
We have identified and purified a platelet integral membrane protein (140,000 mol wt), using the KC4 monoclonal antibody specific for activated platelets, that is internal in resting platelets but exposed on activated platelets (Hsu-Lin S.-C., C.L. Berman, B.C. Furie, D. August, and B. Furie, 1984, J. Biol. Chem. 259: 9121-9126.). The expression of the protein on the platelet surface is secretion-dependent. This protein has been named platelet activation-dependent granule-external membrane (PADGEM) protein. PADGEM protein is distinct from the surface glycoproteins of resting platelets, but identical to the S12 antigen, GMP-140. Using immunofluorescent staining, resting platelets failed to stain for PADGEM protein with the KC4 antibody, but after permeabilization showed a punctate staining of the cell interior. Thrombin-stimulated intact platelets stained with a peripheral rim pattern thus demonstrating the translocation of PADGEM protein from an internal location to the cell surface. PADGEM protein expression on the platelet surface at varying thrombin concentrations correlated with alpha granule release, as measured by the secretion of platelet factor 4. Further evidence for an alpha granule localization of PADGEM protein was provided by nitrogen cavitation of resting platelets followed by metrizamide density gradient centrifugation; PADGEM protein codistributed with platelet factor 4. Using immunoelectron microscopy, the protein was localized to the alpha granule in frozen ultrathin sections of resting platelets labeled using rabbit anti-PADGEM protein antibodies, whereas in thrombin-activated platelets, the plasma membrane was labeled. These studies indicate that PADGEM protein is a component of the alpha granule membrane of resting platelets and is incorporated into the plasma membrane upon activation and secretion.
我们利用针对活化血小板的KC4单克隆抗体,鉴定并纯化了一种血小板整合膜蛋白(分子量140,000),该蛋白在静息血小板中位于内部,但在活化血小板中暴露于表面(Hsu-Lin S.-C., C.L. Berman, B.C. Furie, D. August, and B. Furie, 1984, J. Biol. Chem. 259: 9121-9126.)。该蛋白在血小板表面的表达依赖于分泌。这种蛋白被命名为血小板活化依赖性颗粒外周膜(PADGEM)蛋白。PADGEM蛋白与静息血小板的表面糖蛋白不同,但与S12抗原、GMP-140相同。使用免疫荧光染色,静息血小板用KC4抗体对PADGEM蛋白染色呈阴性,但通透处理后细胞内部呈点状染色。凝血酶刺激的完整血小板呈外周边缘模式染色,从而证明PADGEM蛋白从内部位置转运到细胞表面。不同凝血酶浓度下血小板表面PADGEM蛋白的表达与α颗粒释放相关,这通过血小板因子4的分泌来衡量。静息血小板经氮空化后进行Metrizamide密度梯度离心,为PADGEM蛋白定位于α颗粒提供了进一步证据;PADGEM蛋白与血小板因子4共分布。使用免疫电子显微镜,在用兔抗PADGEM蛋白抗体标记的静息血小板冷冻超薄切片中,该蛋白定位于α颗粒,而在凝血酶活化的血小板中,质膜被标记。这些研究表明,PADGEM蛋白是静息血小板α颗粒膜的一个组成部分,在活化和分泌时整合到质膜中。