Newly Developed Mg2+–Selective Fluorescent Probe Enables Visualization of Mg2+ Dynamics in Mitochondria

摘要

Mg²⁺ plays important roles in numerous cellular functions. Mitochondria take part in intracellular Mg²⁺ regulation and the Mg²⁺ concentration in mitochondria affects the synthesis of ATP. However, there are few methods to observe Mg²⁺ in mitochondria in intact cells. Here, we have developed a novel Mg²⁺–selective fluorescent probe, KMG-301, that is functional in mitochondria. This probe changes its fluorescence properties solely depending on the Mg²⁺ concentration in mitochondria under physiologically normal conditions. Simultaneous measurements using this probe together with a probe for cytosolic Mg²⁺, KMG-104, enabled us to compare the dynamics of Mg²⁺ in the cytosol and in mitochondria. With this method, carbonyl cyanide p-(trifluoromethoxy) phenylhydrazone (FCCP)–induced Mg²⁺ mobilization from mitochondria to the cytosol was visualized. Although a FCCP–induced decrease in the Mg²⁺ concentration in mitochondria and an increase in the cytosol were observed both in differentiated PC12 cells and in hippocampal neurons, the time-courses of concentration changes varied with cell type. Moreover, the relationship between mitochondrial Mg²⁺ and Parkinson's disease was analyzed in a cellular model of Parkinson's disease by using the 1-methyl-4-phenylpyridinium ion (MPP⁺). A gradual decrease in the Mg²⁺ concentration in mitochondria was observed in response to MPP⁺ in differentiated PC12 cells. These results indicate that KMG-301 is useful for investigating Mg²⁺ dynamics in mitochondria. All animal procedures to obtain neurons from Wistar rats were approved by the ethical committee of Keio University (permit number is 09106-(1)).