The quantal nature of calcium release to caffeine in single smooth muscle cells results from activation of the sarcoplasmic reticulum Ca(2+)-ATPase
Steenbergen, Josef M. ; Fay, Fredric S.
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UMass Chan Affiliations
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Keywords
Animals
Bufo marinus
Caffeine
Calcium
Calcium Channels
Calcium-Transporting ATPases
Cell Compartmentation
Cell Membrane Permeability
Cells, Cultured
Detergents
Dose-Response Relationship, Drug
Enzyme Activation
Enzyme Inhibitors
Ion Channel Gating
Muscle Proteins
Muscle, Smooth
Ryanodine Receptor Calcium Release Channel
Saponins
Sarcoplasmic Reticulum
Terpenes
Thapsigargin
Life Sciences
Medicine and Health Sciences
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Abstract
Calcium release from intracellular stores occurs in a graded manner in response to increasing concentrations of either inositol 1,4,5-trisphosphate or caffeine. To investigate the mechanism responsible for this quantal release phenomenon, [Ca2+] changes inside intracellular stores in isolated single smooth muscle cells were monitored with mag-fura 2. Following permeabilization with saponin or alpha-toxin the dye, loaded via its acetoxymethyl ester, was predominantly trapped in the sarcoplasmic reticulum (SR). Low caffeine concentrations in the absence of ATP induced only partial Ca2+ release; however, after inhibiting the calcium pump with thapsigargin the same stimulus released twice as much Ca2+. When the SR Ca(2+)-ATPase was rendered non-functional by depleting its "ATP pool," submaximal caffeine doses almost fully emptied the stores of Ca2+. We conclude that quantal release of Ca2+ in response to caffeine in these smooth muscle cells is largely due to the activity of the SR Ca(2+)-ATPase, which appears to return a portion of the released Ca2+ back to the SR, even in the absence of ATP. Apparently the SR Ca(2+)-ATPase is fueled by ATP, which is either compartmentalized or bound to the SR.
Source
J Biol Chem. 1996 Jan 26;271(4):1821-4.