Washida S
Acta Med Okayama. 1978 Jun;32(2):159-67.
Binding of bacterial endotoxin to platelets, erythrocytes, lymphocytes and granulocytes was examined by using diffusion dialysis. Platelets, erythrocytes, lymphocytes and granulocytes were fractionated from normal human blood and the binding of endotoxin (LPS: Lipopolysaccharide of E. coli) to each cell fraction was measured at 4 degrees C and the binding efficiency was expressed as a binding index (%d4degreesC +/- SD). The binding index for each cell fraction was as follows; 10.2 +/- 1.6 for platelets, 1.0 +/- 0.9 for erythrocytes, 4.3 +/- 1.6 for lymphocytes and 10.0 +/- 1.5 for granulocytes (n = 11) respectively. Since a platelet possesses a small cell surface area compared with other cells, it was clear that the endotoxin bound preferentially to platelets in vitro. The binding mechanism to the platelet cell surface was suggested to be direct binding of endotoxin to the receptor on platelet cell membrane rather than through an immunologically activated mechanism.
采用扩散透析法检测细菌内毒素与血小板、红细胞、淋巴细胞及粒细胞的结合情况。从正常人血液中分离出血小板、红细胞、淋巴细胞及粒细胞,于4℃测定内毒素(脂多糖:大肠杆菌脂多糖)与各细胞组分的结合情况,结合效率以结合指数(%d4℃±标准差)表示。各细胞组分的结合指数如下:血小板为10.2±1.6,红细胞为1.0±0.9,淋巴细胞为4.3±1.6,粒细胞为10.0±1.5(n = 11)。由于与其他细胞相比,血小板的细胞表面积较小,因此很明显内毒素在体外优先与血小板结合。提示内毒素与血小板细胞表面的结合机制是内毒素直接与血小板细胞膜上的受体结合,而非通过免疫激活机制。