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A Basis of the Crenation of Erythrocyte Ghosts by Electrolytes

机译:电解质促成红细胞重影的基础

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Erythrocyte ghosts isolated in hemolytic hypotonic buffers, pH 7.0-8.0, 0-4oC were previously observed to be crenated by electrolytes. This shape transformation, which occurred rapidly and reversibly, was attributed to electrostatic interactions of cations with flexible filamentous anionic spectrin, the major protein component of the skeleton and/or anionic phospholipids, since divalent cationic salts crenated at concentrations substantially lower than those of monovalent cationic salts and that crenation appeared unrelated to the anion species. However, crenation by electrolytes was markedly influenced by ionic conditions and temperature. A mechanism of the erythrocyte shape control has been previously suggested in which band 3 (AE1), exchanging the monovalent anions Cl- and HCO3 - and linked to spectrin, plays a pivotal role. Briefly, the alternative recruitment of its inward-facing (band 3i) and outward-facing (band 3o) conformations contract and relax the skeleton, thereby promoting echinocytosis and stomatocytosis, respectively. Band 3 transports also other anions, including endogenous inorganic phosphate, but at a slow rate. This mechanism would explain the above observations and would lead to some inferences, one of which is a Cl--dependent crenation by Mg2+ and Ca2+, suggesting that they specifically bind on sites on spectrin.
机译:先前观察到在溶血性低渗缓冲液(pH 7.0-8.0,0-4oC)中分离出的红血球鬼魂被电解质腐蚀。这种形状变化迅速而可逆地发生,归因于阳离子与挠性丝状阴离子血影蛋白(骨架和/或阴离子磷脂的主要蛋白质成分)之间的静电相互作用,因为二价阳离子盐的ren杂度大大低于一价阳离子盐的浓度。盐和这种起皱现象似乎与阴离子种类无关。但是,电解质引起的起皱受到离子条件和温度的显着影响。先前已经提出了红细胞形状控制的机制,其中交换单价阴离子Cl-和HCO3-并与血影蛋白相连的条带3(AE1)起着关键作用。简而言之,其向内(带3i)构型和向外(带3o)构型的替代募集收缩并松弛骨骼,从而分别促进嗜碱性细胞增多和气孔增多。带3还以缓慢的速度传输其他阴离子,包括内源性无机磷酸根。这种机制将解释上述观察结果,并得出一些推论,其中之一是Mg2 +和Ca2 +对Cl的依赖,这表明它们特异性结合在血影蛋白上。

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