Yang Yang, Koo Stephanie, Heng Li Tze, Meiselman Herbert J, Neu Björn
Division of Bioengineering, School of Chemical and Biomedical Engineering, Nanyang Technological University, Singapore.
Biochim Biophys Acta. 2014 Jan;1840(1):288-93. doi: 10.1016/j.bbagen.2013.09.031. Epub 2013 Sep 27.
Abnormal adhesion of red blood cells (RBCs) to vascular endothelium is often associated with reduced levels of sialic acids on RBC membranes and with elevated levels of pro-adhesive plasma proteins. However, the synergistic effects of these two factors on the adhesion are not clear. In this work, we tested the hypothesis that macromolecular depletion interaction originating from non-adsorbing macromolecules can promote the adhesion of RBCs with reduced sialic acid content to the endothelium.
RBCs are treated with neuraminidase to specifically remove sialic acids from their surface followed by the evaluation of their deformability, zeta potential and membrane proteins. The adhesion of these enzyme-treated RBCs to cultured human umbilical vein endothelial cells (ECs) is studied in the presence of 70 or 500kDa dextran with a flow chamber assay.
Our results demonstrate that removal of sialic acids from RBC surface can induce erythrocyte adhesion to endothelial cells and that such adhesion is significantly enhanced in the presence of high-molecular weight dextran. The adhesion-promoting effect of dextran exhibits a strong dependence on dextran concentration and molecular mass, and it is concluded to originate from macromolecular depletion interaction.
These results suggest that elevated levels of non-adsorbing macromolecules in plasma might play a significant role in promoting endothelial adhesion of erythrocytes with reduced sialic acids.
Our findings should therefore be of great value in understanding abnormal RBC-EC interactions in pathophysiological conditions (e.g., sickle cell disease and diabetes) and after blood transfusions.
红细胞(RBC)与血管内皮的异常黏附通常与红细胞膜上唾液酸水平降低以及促黏附血浆蛋白水平升高有关。然而,这两个因素对黏附的协同作用尚不清楚。在本研究中,我们检验了以下假设:源自非吸附性大分子的大分子排空相互作用可促进唾液酸含量降低的红细胞与内皮的黏附。
用神经氨酸酶处理红细胞以特异性去除其表面的唾液酸,随后评估其变形性、zeta电位和膜蛋白。使用流动腔试验研究这些经酶处理的红细胞在存在70kDa或500kDa葡聚糖的情况下与培养的人脐静脉内皮细胞(EC)的黏附。
我们的结果表明,从红细胞表面去除唾液酸可诱导红细胞与内皮细胞黏附,并且在存在高分子量葡聚糖的情况下这种黏附会显著增强。葡聚糖的促黏附作用对葡聚糖浓度和分子量有很强的依赖性,并且得出结论认为其源自大分子排空相互作用。
这些结果表明,血浆中升高的非吸附性大分子水平可能在促进唾液酸含量降低的红细胞与内皮的黏附中起重要作用。
因此,我们的发现对于理解病理生理状况(如镰状细胞病和糖尿病)以及输血后异常的红细胞-内皮细胞相互作用具有重要价值。