首页> 外文期刊>Biochemistry (Moscow). Supplement, Series A. Membrane and cell biology >The role of red blood cell adenylyl cyclase activation in changes of erythrocyte membrane microrheological properties
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The role of red blood cell adenylyl cyclase activation in changes of erythrocyte membrane microrheological properties

机译:红细胞腺苷酸环化酶激活在红细胞膜微流变性质变化中的作用

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The ability of red blood cells (RBCs) for the reversible change of their shape under passing through capillaries in microcirculation mainly depends on membrane elasticity of these cells. Phosphorylation of some membrane proteins can result in the changes of microrheological red blood cell properties. Here we show a significant increase in RBC deformability (RBCD) after incubation with isoproterenol (10 ~(-6) M). Red blood cell aggregation (RBCA) decreased under these conditions only slightly. When forskolin (10 μM), an adenylyl cyclase (AC) stimulator, was added to the RBC suspension, RBCD increased significantly (p < 0.05). Some more changes of deformability were found after incubation of RBC with stable penetrating analog of cyclic adenosine phosphate (cAMP), dibutyryl-cAMP, (dB-cAMP, 50 μM) and after phosphodiesterase (PDE) activity inhibition with Vinpocetine, Rolipram, or IBMX. It was found that Gs-proteins inhibitor Clonidine and specific Gi-protein stimulator Mastaparan 7 increased both RBCD and RBCA. On the whole, the data clearly show that the RBC aggregation and deformation changes are related with activation of the different intracellular signaling pathways. We suppose that RBCD increase was mainly associated with activation of the adenylyl-cyclase-cAMP system.
机译:红细胞(RBC)在微循环中通过毛细血管后其形状可逆变化的能力主要取决于这些细胞的膜弹性。一些膜蛋白的磷酸化可导致微流变红细胞特性的变化。在这里,我们显示了与异丙肾上腺素(10〜(-6)M)孵育后RBC变形性(RBCD)的显着增加。在这些条件下,红细胞聚集(RBCA)仅略有下降。当福斯可林(10μM),腺苷酸环化酶(AC)刺激物添加到RBC悬浮液中时,RBCD显着增加(p <0.05)。在将RBC与稳定的环状磷酸腺苷(cAMP),二丁酰-cAMP(dB-cAMP,50μM)的稳定渗透类似物孵育后以及在用长春西汀,Rolipram或IBMX抑制磷酸二酯酶(PDE)活性后,发现了更多的可变形性变化。 。发现Gs蛋白抑制剂可乐定和特定的Gi蛋白刺激剂Mastaparan 7均可增加RBCD和RBCA。总体而言,数据清楚地表明,RBC的聚集和变形变化与不同细胞内信号通路的激活有关。我们认为RBCD的增加主要与腺苷酸环化酶cAMP系统的激活有关。

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