Dupont Geneviève, Combettes Laurent
Unité de Chronobiologie Théorique, Faculté des Sciences, Université Libre de Bruxelles (ULB), Brussels, Belgium.
Interactions Cellulaires et Physiopathologie Hépatique, UMR-S 1174, Université Paris Sud, Orsay, France.
F1000Res. 2016 Aug 19;5. doi: 10.12688/f1000research.8438.1. eCollection 2016.
Ca (2+) oscillations, a widespread mode of cell signaling, were reported in non-excitable cells for the first time more than 25 years ago. Their fundamental mechanism, based on the periodic Ca (2+) exchange between the endoplasmic reticulum and the cytoplasm, has been well characterized. However, how the kinetics of cytosolic Ca (2+) changes are related to the extent of a physiological response remains poorly understood. Here, we review data suggesting that the downstream targets of Ca (2+) are controlled not only by the frequency of Ca (2+) oscillations but also by the detailed characteristics of the oscillations, such as their duration, shape, or baseline level. Involvement of non-endoplasmic reticulum Ca (2+) stores, mainly mitochondria and the extracellular medium, participates in this fine tuning of Ca (2+) oscillations. The main characteristics of the Ca (2+) exchange fluxes with these compartments are also reviewed.
钙(Ca²⁺)振荡是一种广泛存在的细胞信号传导模式,早在25年多前就首次在非兴奋性细胞中被报道。其基于内质网与细胞质之间周期性钙(Ca²⁺)交换的基本机制已得到充分表征。然而,胞质钙(Ca²⁺)变化的动力学如何与生理反应的程度相关,目前仍知之甚少。在此,我们回顾相关数据,这些数据表明钙(Ca²⁺)的下游靶点不仅受钙(Ca²⁺)振荡频率的控制,还受振荡的详细特征(如持续时间、形状或基线水平)的控制。非内质网钙(Ca²⁺)储存库(主要是线粒体和细胞外介质)的参与,也参与了钙(Ca²⁺)振荡的这种精细调节。本文还回顾了与这些区室进行钙(Ca²⁺)交换通量的主要特征。