National Centre for Biological Sciences, Tata Institute of Fundamental Research Bangalore, India.
Front Neural Circuits. 2010 Mar 30;4:10. doi: 10.3389/fncir.2010.00010. eCollection 2010.
In neurons a well-defined source of signaling Ca(2+) is the extracellular medium. However, as in all metazoan cells, Ca(2+) is also stored in endoplasmic reticular compartments inside neurons. The relevance of these stores in neuronal function has been debatable. The Orai gene encodes a channel that helps refill these stores from the extracellular medium in non-excitable cells through a process called store-operated Ca(2+) entry or SOCE. Recent findings have shown that raising the level of Orai or its activator STIM, and consequently SOCE in neurons, can restore flight to varying extents to Drosophila mutants for an intracellular Ca(2+)-release channel - the inositol 1,4,5-trisphosphate receptor (InsP(3)R). Both intracellular Ca(2+)-release and SOCE appear to function in neuro-modulatory domains of the flight circuit during development and acute flight. These findings raise exciting new possibilities for the role of SOCE in vertebrate motor circuit function and the treatment of neurodegenerative disorders where intracellular Ca(2+) signaling has been implicated as causative.
在神经元中,一个明确的信号转导 Ca(2+) 来源是细胞外介质。然而,正如所有后生动物细胞一样,Ca(2+) 也储存在神经元内部的内质网隔室中。这些储存库在神经元功能中的相关性一直存在争议。Orai 基因编码一种通道,可帮助非兴奋细胞通过称为储存操作 Ca(2+) 内流或 SOCE 的过程从细胞外介质中重新填充这些储存库。最近的研究发现,提高 Orai 或其激活剂 STIM 的水平,从而提高神经元中的 SOCE,可以在不同程度上恢复飞行,使果蝇突变体中的细胞内 Ca(2+) 释放通道——三磷酸肌醇受体 (InsP(3)R) 恢复飞行。细胞内 Ca(2+) 释放和 SOCE 似乎都在发育和急性飞行期间的飞行回路的神经调节域中发挥作用。这些发现为 SOCE 在脊椎动物运动回路功能中的作用以及治疗涉及细胞内 Ca(2+) 信号作为病因的神经退行性疾病提供了令人兴奋的新可能性。