Wong P
Laboratoire de Chimie des Protéines, Montréal, QC, Canada.
Clin Hemorheol Microcirc. 2018;68(4):383-389. doi: 10.3233/CH-170292.
It is proposed that the specific reversal by serum albumin of the erythrocyte echinocytosis in an inorganic phosphate buffer saline or in a saline, either after 24 h in blood or after a storage of 6-7 weeks in SGAM or PAGGSM media, is due to a cell dehydration by a decrease of the total NaCl and KCl concentrations favoring the stomatocytogenic slow outward transport of inorganic phosphate with a hydrogen ion by band 3 anion exchanger, which was previously proposed to control the erythrocyte shape. This proposal would indicate that the opposition of the erythrocyte echinocytosis by serum albumin is not limited to binding to echinocytogenic amphiphiles, supported by the ability of the band 3-based mechanism of control of the erythrocyte shape to explain a variety of observations on the erythrocyte shape. It would also imply that this mechanism is a determinant of the erythrocyte rheological properties since influenced by cell shape and volume. It is shown that the above process of stomatocytosis can explain stomatocytoses by different agents as well as a knizocytosis induced in vitro and occurring in acquired and inherited disorders and other situations. Lastly, it can also explain the opposition of hemolysis by mannitol in SGAM and PAGGSM media.
有人提出,血清白蛋白能特异性逆转无机磷酸盐缓冲盐水或盐水中红细胞的棘状红细胞增多症,无论是在血液中放置24小时后,还是在SGAM或PAGGSM培养基中储存6 - 7周后,这是由于总氯化钠和氯化钾浓度降低导致细胞脱水,有利于带3阴离子交换剂介导的无机磷酸盐与氢离子的口形细胞生成性缓慢外向转运,此前有人提出该交换剂可控制红细胞形状。这一观点表明,血清白蛋白对红细胞棘状红细胞增多症的对抗作用不仅限于与棘状红细胞生成性两亲分子结合,基于带3的红细胞形状控制机制能够解释关于红细胞形状的各种观察结果,这为上述观点提供了支持。这还意味着该机制是红细胞流变学特性的一个决定因素,因为它受细胞形状和体积的影响。研究表明,上述口形细胞生成过程可以解释不同因素导致的口形细胞增多症,以及体外诱导并发生在获得性和遗传性疾病及其他情况下的皱缩红细胞增多症。最后,它还可以解释甘露醇在SGAM和PAGGSM培养基中对溶血的对抗作用。