Rosado J A, Graves D, Sage S O
Department of Physiology, University of Cambridge, Downing Street, Cambridge CB2 3EG, UK.
Biochem J. 2000 Oct 15;351 Pt 2(Pt 2):429-37.
We have recently reported that store-mediated Ca(2+) entry in platelets is likely to be mediated by a reversible trafficking and coupling of the endoplasmic reticulum with the plasma membrane, a model termed 'secretion-like coupling'. In this model the actin cytoskeleton plays a key regulatory role. Since tyrosine kinases have been shown to be important for Ca(2+) entry in platelets and other cells, we have now investigated the possible involvement of tyrosine kinases in the secretion-like-coupling model. Treatment of platelets with thrombin or thapsigargin induced actin polymerization by a calcium-independent pathway. Methyl 2,5-dihydroxycinnamate, a tyrosine kinase inhibitor, prevented thrombin- or thapsigargin-induced actin polymerization. The effects of tyrosine kinases in store-mediated Ca(2+) entry were found to be entirely dependent on the actin cytoskeleton. PP1, an inhibitor of the Src family of proteins, partially inhibited store-mediated Ca(2+) entry. In addition, depletion of intracellular Ca(2+) stores stimulated cytoskeletal association of the cytoplasmic tyrosine kinase pp60(src), a process that was sensitive to treatment with cytochalasin D and PP1, but not to inhibition of Ras proteins using prenylcysteine analogues. Finally, combined inhibition of both Ras proteins and tyrosine kinases resulted in complete inhibition of Ca(2+) entry, suggesting that these two families of proteins have independent effects in the activation of store-mediated Ca(2+) entry in human platelets.
我们最近报道,血小板中储存介导的Ca(2+)内流可能是由内质网与质膜的可逆运输和偶联介导的,该模型称为“分泌样偶联”。在这个模型中,肌动蛋白细胞骨架起着关键的调节作用。由于酪氨酸激酶已被证明对血小板和其他细胞中的Ca(2+)内流很重要,我们现在研究了酪氨酸激酶在分泌样偶联模型中的可能作用。用凝血酶或毒胡萝卜素处理血小板通过钙非依赖性途径诱导肌动蛋白聚合。酪氨酸激酶抑制剂2,5-二羟基肉桂酸甲酯可阻止凝血酶或毒胡萝卜素诱导的肌动蛋白聚合。发现酪氨酸激酶在储存介导的Ca(2+)内流中的作用完全依赖于肌动蛋白细胞骨架。PP1是Src蛋白家族的抑制剂,部分抑制储存介导的Ca(2+)内流。此外,细胞内Ca(2+)储存的耗尽刺激了细胞质酪氨酸激酶pp60(src)与细胞骨架的结合,这一过程对细胞松弛素D和PP1处理敏感,但对使用异戊烯半胱氨酸类似物抑制Ras蛋白不敏感。最后,联合抑制Ras蛋白和酪氨酸激酶导致Ca(2+)内流完全抑制,表明这两个蛋白家族在激活人血小板中储存介导的Ca(2+)内流方面具有独立作用。