Game L, Voegel J C, Schaaf P, Stoltz J F
Faculté de Chirurgie Dentaire, INSERM U424, Strasbourg, France.
Biochim Biophys Acta. 1996 Oct 24;1291(2):138-42. doi: 10.1016/0304-4165(96)00056-6.
Under physiological conditions, red blood cells (RBCs) form aggregates that allow blood flow in all the circulatory system. RBC aggregation is the result of local flow shear stress, erythrocyte properties and macromolecular interactions between adjacent cells. Plasma proteins like fibrinogen or IgG are considered to promote RBC aggregation by a mechanism that remains to be explained. In the present study, we have examined the precise role of IgG on RBC fast-phase aggregation, in comparison with that of fibrinogen. Under our experimental conditions, we observed no fast-phase aggregating effect for IgG, at either physiological or supraphysiological concentrations, while fibrinogen induces strong aggregation of RBC. We also suspect the other plasma proteins to play a role in the RBC aggregating process.
在生理条件下,红细胞(RBCs)形成聚集体,使血液能够在整个循环系统中流动。红细胞聚集是局部血流剪切应力、红细胞特性以及相邻细胞之间大分子相互作用的结果。血浆蛋白如纤维蛋白原或免疫球蛋白G(IgG)被认为通过一种尚待解释的机制促进红细胞聚集。在本研究中,我们已将免疫球蛋白G与纤维蛋白原相比较,研究了其对红细胞快速聚集阶段的确切作用。在我们的实验条件下,无论在生理浓度还是超生理浓度下,我们均未观察到免疫球蛋白G有快速聚集效应,而纤维蛋白原可诱导红细胞强烈聚集。我们还怀疑其他血浆蛋白在红细胞聚集过程中发挥作用。