Mitochondrial Ca2+ uniporter and CaMKII in heart.

Abstract

The influx of cytosolic Ca²⁺ into mitochondria is mediated primarily by the mitochondrial calcium uniporter (MCU), a small-conductance, Ca²⁺-selective channel^-. MCU modulates intracellular Ca²⁺ 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 (<i>I_MCU</i>) 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 <i>I_MCU</i> 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.