Abstract
Many studies of Ca
effects on mitochondrial respiration in intact cells have used electrical and/or chemical stimulation to elevate intracellular [Ca
], and have reported increases in [NADH] and increased ADP/ATP ratios as dominant controllers of respiration. This study tested a different form of stimulation: brief temperature increases produced by pulses of infrared light (IR, 1863 nm, 8-10
C for ~5 s). Fluorescence imaging techniques applied to single PC-12 cells in low µM extracellular [Ca
] revealed IR stimulation-induced increases in both cytosolic (fluo5F) and mitochondrial (rhod2) [Ca
[. IR stimulation increased O
consumption (porphyrin fluorescence), and produced an alkaline shift in mitochondrial matrix pH (Snarf1), indicating activation of the electron transport chain (ETC). The increase in O
consumption persisted in oligomycin, and began during a decrease in NADH, suggesting that the initial increase in ETC activity was not driven by increased ATP synthase activity or an increased fuel supply to ETC complex I. Imaging with two potentiometric dyes (TMRM and R123) indicated a depolarizing shift in ΔΨ
that persisted in high [K
] medium. High-resolution fluorescence imaging disclosed large, reversible mitochondrial depolarizations that were inhibited by cyclosporin A (CSA), consistent with opening of transient mitochondrial permeability transition pores. IR stimulation also produced a Ca
-dependent increase in superoxide production (Mitosox) that was not inhibited by CSA, indicating that the increase in superoxide did not require transition pore opening. Thus the intracellular Ca
release that follows pulses of infrared light offers new insights into Ca
-dependent processes controlling respiration and reactive oxygen species in intact cells.
