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引用次数: 0
摘要
信号机制的动态变化可能编码对细胞调节至关重要的特定信息。破译这些信息需要对活细胞中的关键信号分子进行精密的测量。Teruel和Meyer提出了一种方法,可以测量在玻璃显微镜载玻片上生长的许多单个活大鼠嗜碱性白血病细胞中荧光标记的蛋白激酶Cγ (PKCγ)到细胞膜的钙依赖性易位。酶表现出两种不同的反应模式。当钙从内部储存中释放出来时,PKCγ会短暂地移动到细胞表面,仅持续几秒钟。然而,导致细胞外钙进入的信号导致酶持续易位到细胞表面,持续时间超过半分钟。细胞主要表现为前者对低剂量血小板活化因子的反应,后者对大剂量血小板活化因子的反应。研究结果有助于解释像钙这样的普通信使如何控制离散的细胞反应。M. N. Teruel, T. Meyer,受体触发的钙传感蛋白模块膜易位的平行单细胞监测。科学295,1910-1912(2002)。【摘要】【全文】
Dynamic changes in signaling mechanisms may encode specific information critical to cellular regulation. Deciphering these messages requires sophisticated measurements of key signaling molecules in living cells. Teruel and Meyer present a method that allows measurement of calcium-dependent translocation of fluorescently tagged protein kinase Cγ (PKCγ) to the cell membrane in many single, living rat basophilic leukemia cells grown on glass microscope slides. The enzyme showed two distinct modes of response. When calcium was released from internal stores, there was transient movement of PKCγ to the cell surface for only a few seconds. However, signals that caused entry of extracellular calcium caused a persistent translocation of the enzyme to the cell surface that lasted for more than half a minute. Cells showed primarily the former response to low doses of platelet activation factor, and the latter response to larger doses. The results help explain how a common messenger like calcium can control discrete cellular responses. M. N. Teruel, T. Meyer, Parallel single-cell monitoring of receptor-triggered membrane translocation of a calcium-sensing protein module. Science 295, 1910-1912 (2002). [Abstract] [Full Text]