IN Xenopus oocytes, as well as other cells, inositol-1,4,5-trisphospha
te (Ins(1,4,5)P-3)-induced Ca2+ release(1-4) is an excitable process t
hat generates propagating Ca2+ waves(5-7) that annihilate upon collisi
on(8-12). The fundamental property responsible for excitability appear
s to be the Ca2+ dependency of the Ins(1,4,5)P-3 receptor(9). Here we
report that Ins(1,4,5)P-3-induced Ca2+ were activity is strengthened b
y oxidizable substrates that energize mitochrondria, increasing Ca2+ w
ave amplitude, velocity and interwave period. The effects of pyruvate/
malate are blocked by ruthenium red at the Ca2+ uniporter, by rotenone
at complex I, and by antimycin A at complex III, and are subsequently
rescued at complex IV by ascorbate tetramethylphenylenediamine (TMPD)
(14). Our data reveal that potential-driven mitochondrial Ca2+ uptake
is a major factor in the regulation of Ins(1,4,5)P-3-induced Ca2+ rele
ase and clearly demonstrate a physiological role of mitrochondria in i
ntracellular Ca2+ signalling.