Department of Physiology, University of California San Francisco, San Francisco, California 94158, USA.
Department of Biochemistry and Molecular Biology, Stark Neuroscience Research Institute, Indiana University School of Medicine, Indianapolis, Indiana 46202, USA.
Nature. 2014 Sep 25;513(7519):E1-2. doi: 10.1038/nature13626.
The influx of cytosolic Ca into mitochondria is mediated primarily by the mitochondrial calcium uniporter (MCU), a small-conductance, Ca-selective channel. MCU modulates intracellular Ca transients and regulates ATP production and cell death. Recently, Joiner et al. reported that MCU is regulated by mitochondrial CaMKII, and this regulation determines stress response in heart. They reported a very large current putatively mediated by MCU that was about two orders of magnitude greater than the MCU current () that we previously measured in heart mitochondria. Also, the current traces presented by Joiner et al. showed unusually high fluctuations incompatible with the low single-channel conductance of MCU. Here we performed patch-clamp recordings from mouse heart mitochondria under the exact conditions used by Joiner et al. We confirmed that in cardiomyocytes is very small and showed that it is not directly regulated by CaMKII. Thus the currents presented by Joiner et al. do not correspond to MCU, and there is no direct electrophysiological evidence that CaMKII regulates MCU.
胞浆钙离子流入线粒体主要由线粒体钙单向转运体(MCU)介导,MCU 是一种小电导、钙离子选择性通道。MCU 调节细胞内钙离子瞬变,调节 ATP 产生和细胞死亡。最近,Joiner 等人报道 MCU 受线粒体钙调蛋白激酶 II(CaMKII)调节,这种调节决定了心脏的应激反应。他们报道了一种推测由 MCU 介导的非常大的电流,比我们之前在心脏线粒体中测量到的 MCU 电流()大两个数量级。此外,Joiner 等人呈现的电流轨迹显示出异常高的波动,与 MCU 的低单通道电导不兼容。在这里,我们在与 Joiner 等人使用的完全相同的条件下进行了来自小鼠心脏线粒体的膜片钳记录。我们证实,在心肌细胞中非常小,并且表明它不受 CaMKII 的直接调节。因此,Joiner 等人呈现的电流与 MCU 不对应,也没有直接的电生理证据表明 CaMKII 调节 MCU。