Lawrie A M, Toescu E C, Gallacher D V
Physiological Laboratory, Liverpool University, UK.
Cell Calcium. 1993 Nov;14(10):698-710. doi: 10.1016/0143-4160(93)90096-o.
The oscillations in cytosolic Ca2+ evoked in pancreatic exocrine acinar cells by submaximal concentrations of the two phosphoinositidase-coupled agonists acetylcholine (ACh) and cholecystokinin octapeptide (CCK-8) have very different temporal patterns. In the present study we use digital video imaging of Fura-2 fluorescence to map the spatial distribution of Ca2+ during the oscillating responses to these two agonists. The spatial patterns induced are very different for each of these agonists. ACh oscillations are sinusoidal and initiated at the secretory pole of these morphologically and functionally polarized cells. As they spread across the cell, pronounced gradients in Ca2+ develop that persist throughout the oscillating response. CCK-8 induces a series of discrete Ca2+ transients of longer duration and lower frequency. These elevations in Ca2+ arise slowly, throughout the cells and without any detectable gradients in Ca2+. We consider that the different spatiotemporal patterns can be explained on the basis of a physiologically relevant interaction between Ins(1,4,5)P3 and protein kinase C in second messenger-mediated Ca2+ signalling.
亚最大浓度的两种与磷酸肌醇酶偶联的激动剂乙酰胆碱(ACh)和八肽胆囊收缩素(CCK-8)在胰腺外分泌腺泡细胞中诱发的胞质Ca2+振荡具有非常不同的时间模式。在本研究中,我们使用Fura-2荧光的数字视频成像来绘制在对这两种激动剂的振荡反应过程中Ca2+的空间分布。这两种激动剂各自诱导的空间模式非常不同。ACh振荡呈正弦波,在这些形态和功能极化细胞的分泌极起始。当它们在细胞中传播时,Ca2+会形成明显的梯度,并在整个振荡反应过程中持续存在。CCK-8诱导一系列持续时间更长、频率更低的离散Ca2+瞬变。这些Ca2+升高在整个细胞中缓慢出现,且没有任何可检测到的Ca2+梯度。我们认为,不同的时空模式可以基于第二信使介导的Ca2+信号传导中Ins(1,4,5)P3与蛋白激酶C之间生理相关的相互作用来解释。