Smith B D, La Celle P L, Siefring G E, Lowe-Krentz L, Lorand L
J Membr Biol. 1981;61(2):75-80. doi: 10.1007/BF02007633.
Excess calcium binding affects the shape and dynamics of cellular deformation of human erythrocytes. It may be hypothesized that incorporation of calcium may modify cellular deformability by processes which include specific cross-linking of membrane proteins with resultant changes in cell shape and deformability. Since previous studies indicate that accumulation of calcium ions causes development of gamma-glutamyl-epsilon-lysine bridges in membrane proteins, under control of a membrane transamidating enzyme which specifically requires calcium ions for activation, experiments were devised to examine the relationship between cross-linking and deformability and to determine the effects of specific inhibitor of membrane protein cross-linking on the calcium-dependent modification of erythrocyte to the echinocytic shape. The elastic shear modulus of the membrane was not significantly affected by calcium-induced cross-linking, indicating that induced shape change, not altered elasticity, causes the observed reduction in cellular deformability. These findings support the interpretation that Ca++-induced and transamidase-catalyzed cross-linking of membrane proteins contributes to fixation of altered cellular shape and decreased cellular deformability.
过量的钙结合会影响人类红细胞细胞变形的形状和动力学。可以推测,钙的掺入可能通过包括膜蛋白特异性交联从而导致细胞形状和变形性改变的过程来改变细胞的可变形性。由于先前的研究表明,在一种特别需要钙离子激活的膜转酰胺酶的控制下,钙离子的积累会导致膜蛋白中γ-谷氨酰-ε-赖氨酸桥的形成,因此设计了实验来研究交联与可变形性之间的关系,并确定膜蛋白交联的特异性抑制剂对红细胞向棘状细胞形状的钙依赖性修饰的影响。膜的弹性剪切模量不受钙诱导交联的显著影响,这表明诱导的形状变化而非弹性改变导致了观察到的细胞可变形性降低。这些发现支持了这样的解释,即Ca++诱导的和转酰胺酶催化的膜蛋白交联有助于固定改变的细胞形状并降低细胞可变形性。