Department of Chemosensation, Institute for Biology II, RWTH-Aachen University, Aachen, Germany.
J Physiol. 2011 Nov 1;589(Pt 21):5033-55. doi: 10.1113/jphysiol.2011.216309. Epub 2011 Aug 22.
Intimate bidirectional communication between Sertoli cells and developing germ cells ensures the integrity and efficiency of spermatogenesis. Yet, a conceptual mechanistic understanding of the physiological principles that underlie Sertoli cell autocrine and paracrine signalling is lacking. Here, we characterize a purinergic Ca(2+) signalling network in immature mouse Sertoli cells that consists of both P2X2 and P2Y2 purinoceptor subtypes, the endoplasmic reticulum and, notably, mitochondria. By combining a transgenic mouse model with a dedicated bioluminescence imaging device, we describe a novel method to monitor mitochondrial Ca(2+) mobilization in Sertoli cells at subcellular spatial and millisecond temporal resolution. Our data identify mitochondria as essential components of the Sertoli cell signalling 'toolkit' that control the shape of purinergic Ca(2+) responses, and probably several other paracrine Ca(2+)-dependent signals.
支持细胞和发育中的精原细胞之间的亲密双向通讯确保了精子发生的完整性和效率。然而,对于支持细胞自分泌和旁分泌信号转导所基于的生理原理的概念性机械理解还缺乏。在这里,我们描述了一个在未成熟的小鼠支持细胞中的嘌呤能 Ca(2+)信号网络,该网络由 P2X2 和 P2Y2 嘌呤能受体亚型、内质网以及特别的线粒体组成。通过结合转基因小鼠模型和专用的生物发光成像设备,我们描述了一种新方法,可以以亚细胞空间和毫秒时间分辨率监测支持细胞中线粒体 Ca(2+)的动员。我们的数据表明,线粒体是控制嘌呤能 Ca(2+)反应形状的支持细胞信号“工具包”的重要组成部分,可能还有其他几种旁分泌 Ca(2+)依赖信号。