Larsen E, Celi A, Gilbert G E, Furie B C, Erban J K, Bonfanti R, Wagner D D, Furie B
Division of Hematology/Oncology, New England Medical Center, Boston, Massachusetts.
Cell. 1989 Oct 20;59(2):305-12. doi: 10.1016/0092-8674(89)90292-4.
PADGEM (platelet activation dependent granule-external membrane protein) is an integral membrane protein of the alpha granules of platelets and Weibel-Palade bodies of endothelial cells that is expressed on the plasma membrane upon cell activation and granule secretion. Activated platelets, but not resting platelets, bind to neutrophils, monocytes, HL60 cells, and U937 cells. This interaction is inhibited by anti-PADGEM antibodies, PADGEM, and EDTA; anti-GPIIb-IIIa, anti-thrombospondin, anti-GPIV, and thrombospondin produce no effect. Neutrophils and U937 cells, in contrast to Jurkatt cells, contain PADGEM recognition sites, as shown by binding of PADGEM contained in phospholipid vesicles. These results indicate that PADGEM mediates adhesion of activated platelets to monocytes and neutrophils. Therefore, PADGEM shares not only structural but also functional homology with ELAM-1 and MEL-14, members of a new family of vascular cell adhesion molecules.
血小板活化依赖性颗粒-外膜蛋白(PADGEM)是血小板α颗粒和内皮细胞Weibel-Palade小体的一种整合膜蛋白,在细胞活化和颗粒分泌时表达于质膜上。活化的血小板而非静息血小板能与中性粒细胞、单核细胞、HL60细胞及U937细胞结合。这种相互作用可被抗PADGEM抗体、PADGEM和EDTA抑制;抗血小板糖蛋白IIb-IIIa、抗血小板反应蛋白、抗血小板糖蛋白IV及血小板反应蛋白则无作用。与Jurkatt细胞不同,中性粒细胞和U937细胞含有PADGEM识别位点,如磷脂囊泡中所含PADGEM的结合所示。这些结果表明,PADGEM介导活化血小板与单核细胞及中性粒细胞的黏附。因此,PADGEM不仅与血管细胞黏附分子新家族的成员ELAM-1和MEL-14具有结构同源性,还具有功能同源性。