Literature DB >> 8567621

The quantal nature of calcium release to caffeine in single smooth muscle cells results from activation of the sarcoplasmic reticulum Ca(2+)-ATPase.

J M Steenbergen1, F S Fay.   

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.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8567621     DOI: 10.1074/jbc.271.4.1821

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  18 in total

1.  Multiple pathways responsible for the stretch-induced increase in Ca2+ concentration in toad stomach smooth muscle cells.

Authors:  M T Kirber; A Guerrero-Hernández; D S Bowman; K E Fogarty; R A Tuft; J J Singer; F S Fay
Journal:  J Physiol       Date:  2000-04-01       Impact factor: 5.182

2.  Mechanisms that regulate [Ca2+]i following depolarization in rat systemic arterial smooth muscle cells.

Authors:  T Kamishima; N W Davies; N B Standen
Journal:  J Physiol       Date:  2000-01-15       Impact factor: 5.182

3.  Phosphorylation regulates an inwardly rectifying ATP-sensitive K(+)- conductance in proximal tubule cells of frog kidney.

Authors:  L Robson; M Hunter
Journal:  J Membr Biol       Date:  2005-10       Impact factor: 1.843

4.  Luminal Ca2+ regulates passive Ca2+ efflux from the intracellular stores of hepatocytes.

Authors:  M D Beecroft; C W Taylor
Journal:  Biochem J       Date:  1998-09-01       Impact factor: 3.857

5.  An ATP-gated cation channel with some P2Z-like characteristics in gastric smooth muscle cells of toad.

Authors:  M Ugur; R M Drummond; H Zou; P Sheng; J J Singer; J V Walsh
Journal:  J Physiol       Date:  1997-01-15       Impact factor: 5.182

6.  Quantal release, incremental detection, and long-period Ca2+ oscillations in a model based on regulatory Ca2+-binding sites along the permeation pathway.

Authors:  G Dupont; S Swillens
Journal:  Biophys J       Date:  1996-10       Impact factor: 4.033

7.  'Quantal' calcium release operated by membrane voltage in frog skeletal muscle.

Authors:  G Pizarro; N Shirokova; A Tsugorka; E Ríos
Journal:  J Physiol       Date:  1997-06-01       Impact factor: 5.182

8.  Assessment of intra-SR free [Ca] and buffering in rat heart.

Authors:  T R Shannon; D M Bers
Journal:  Biophys J       Date:  1997-09       Impact factor: 4.033

9.  Slow kinetics of inositol 1,4,5-trisphosphate-induced Ca2+ release: is the release 'quantal' or 'non-quantal'?

Authors:  L Missiaen; H De Smedt; J B Parys; I Sienaert; H Sipma; S Vanlingen; R Casteels
Journal:  Biochem J       Date:  1997-04-01       Impact factor: 3.857

10.  Effects of spaceflight and ground recovery on mesenteric artery and vein constrictor properties in mice.

Authors:  Bradley J Behnke; John N Stabley; Danielle J McCullough; Robert T Davis; James M Dominguez; Judy M Muller-Delp; Michael D Delp
Journal:  FASEB J       Date:  2012-10-25       Impact factor: 5.191

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.