Center for Disease Biology and Integrative Medicine, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.
Cell Calcium. 2010 Mar;47(3):253-63. doi: 10.1016/j.ceca.2009.12.008. Epub 2010 Jan 8.
Intracellular Ca2+ transients are evoked either by the opening of Ca2+ channels on the plasma membrane or by phospholipase C (PLC) activation resulting in IP3 production. Ca2+ wave propagation is known to occur in mechanically stimulated cells; however, it remains uncertain whether and how PLC activation is involved in intracellular Ca2+ wave propagation in mechanically stimulated cells. To answer these questions, it is indispensable to clarify the spatio-temporal relations between intracellular Ca2+ wave propagation and PLC activation. Thus, we visualized both cytosolic Ca2+ and PLC activation using a real-time dual-imaging system in individual Mardin-Darby Canine Kidney (MDCK) cells. This system allowed us to simultaneously observe intracellular Ca2+ wave propagation and PLC activation in a spatio-temporal manner in a single mechanically stimulated MDCK cell. The results showed that PLC was activated not only in the mechanically stimulated region but also in other subcellular regions in parallel with intracellular Ca2+ wave propagation. These results support a model in which PLC is involved in Ca2+ signaling amplification in mechanically stimulated cells.
细胞内 Ca2+ 瞬变是通过质膜上 Ca2+ 通道的开放或通过磷脂酶 C (PLC) 的激活而产生的 IP3 来诱发的。众所周知,Ca2+波在机械刺激细胞中传播;然而,目前尚不确定 PLC 激活是否以及如何参与机械刺激细胞中的细胞内 Ca2+波传播。为了回答这些问题,阐明细胞内 Ca2+波传播和 PLC 激活之间的时空关系是必不可少的。因此,我们使用实时双成像系统在单个 Mardin-Darby Canine Kidney (MDCK) 细胞中可视化细胞内 Ca2+波传播和 PLC 激活。该系统允许我们以时空方式同时观察单个机械刺激的 MDCK 细胞中的细胞内 Ca2+波传播和 PLC 激活。结果表明,PLC 的激活不仅发生在机械刺激区域,而且与细胞内 Ca2+波传播平行发生在其他亚细胞区域。这些结果支持 PLC 参与机械刺激细胞中 Ca2+信号放大的模型。