The quantal nature of calcium release to caffeine in single smooth muscle cells results from activation of the sarcoplasmic reticulum Ca(2+)-ATPase
dc.contributor.author | Steenbergen, Josef M. | |
dc.contributor.author | Fay, Fredric S. | |
dc.date | 2022-08-11T08:10:04.000 | |
dc.date.accessioned | 2022-08-23T16:54:14Z | |
dc.date.available | 2022-08-23T16:54:14Z | |
dc.date.issued | 1996-01-26 | |
dc.date.submitted | 2008-08-15 | |
dc.identifier.citation | <p>J Biol Chem. 1996 Jan 26;271(4):1821-4.</p> | |
dc.identifier.issn | 0021-9258 (Print) | |
dc.identifier.doi | 10.1074/jbc.271.4.1821 | |
dc.identifier.pmid | 8567621 | |
dc.identifier.uri | http://hdl.handle.net/20.500.14038/42455 | |
dc.description.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. | |
dc.language.iso | en_US | |
dc.relation | <p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=8567621&dopt=Abstract">Link to Article in PubMed</a></p> | |
dc.relation.url | https://doi.org/10.1074/jbc.271.4.1821 | |
dc.subject | Adenosine Triphosphate | |
dc.subject | Animals | |
dc.subject | Bufo marinus | |
dc.subject | Caffeine | |
dc.subject | Calcium | |
dc.subject | Calcium Channels | |
dc.subject | Calcium-Transporting ATPases | |
dc.subject | Cell Compartmentation | |
dc.subject | Cell Membrane Permeability | |
dc.subject | Cells, Cultured | |
dc.subject | Detergents | |
dc.subject | Dose-Response Relationship, Drug | |
dc.subject | Enzyme Activation | |
dc.subject | Enzyme Inhibitors | |
dc.subject | Ion Channel Gating | |
dc.subject | Muscle Proteins | |
dc.subject | Muscle, Smooth | |
dc.subject | Ryanodine Receptor Calcium Release Channel | |
dc.subject | Saponins | |
dc.subject | Sarcoplasmic Reticulum | |
dc.subject | Terpenes | |
dc.subject | Thapsigargin | |
dc.subject | Life Sciences | |
dc.subject | Medicine and Health Sciences | |
dc.title | The quantal nature of calcium release to caffeine in single smooth muscle cells results from activation of the sarcoplasmic reticulum Ca(2+)-ATPase | |
dc.type | Journal Article | |
dc.source.journaltitle | The Journal of biological chemistry | |
dc.source.volume | 271 | |
dc.source.issue | 4 | |
dc.identifier.legacycoverpage | https://escholarship.umassmed.edu/oapubs/802 | |
dc.identifier.contextkey | 579687 | |
html.description.abstract | <p>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.</p> | |
dc.identifier.submissionpath | oapubs/802 | |
dc.contributor.department | Department of Physiology | |
dc.source.pages | 1821-4 |