Abstract
The origin of Ibetanull, the Ca2+ current of myotubes from mice lacking the skeletal dihydropyridine receptor (DHPR) beta1a subunit, was investigated. The density of Ibetanull was similar to that of Idys, the Ca2+ current of myotubes from dysgenic mice lacking the skeletal DHPR alpha1S subunit (-0.6 +/- 0.1 and -0.7 +/- 0.1 pA/pF, respectively). However, Ibetanull activated at significantly more positive potentials. The midpoints of the GCa-V curves were 16.3 +/- 1.1 mV and 11.7 +/- 1.0 mV for Ibetanull and Idys, respectively. Ibetanull activated significantly more slowly than Idys. At +30 mV, the activation time constant for Ibetanull was 26 +/- 3 ms, and that for Idys was 7 +/- 1 ms. The unitary current of normal L-type and beta1-null Ca2+ channels estimated from the mean variance relationship at +20 mV in 10 mM external Ca2+ was 22 +/- 4 fA and 43 +/- 7 fA, respectively. Both values were significantly smaller than the single-channel current estimated for dysgenic Ca2+ channels, which was 84 +/- 9 fA under the same conditions. Ibetanull and Idys have different gating and permeation characteristics, suggesting that the bulk of the DHPR alpha1 subunits underlying these currents are different. Ibetanull is suggested to originate primarily from Ca2+ channels with a DHPR alpha1S subunit. Dysgenic Ca2+ channels may be a minor component of this current. The expression of DHPR alpha1S in beta1-null myotubes and its absence in dysgenic myotubes was confirmed by immunofluorescence labeling of cells.
Full Text
The Full Text of this article is available as a PDF (170.2 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Adams B. A., Beam K. G. A novel calcium current in dysgenic skeletal muscle. J Gen Physiol. 1989 Sep;94(3):429–444. doi: 10.1085/jgp.94.3.429. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Adams B. A., Beam K. G. Contractions of dysgenic skeletal muscle triggered by a potentiated, endogenous calcium current. J Gen Physiol. 1991 Apr;97(4):687–696. doi: 10.1085/jgp.97.4.687. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Adams B. A., Tanabe T., Mikami A., Numa S., Beam K. G. Intramembrane charge movement restored in dysgenic skeletal muscle by injection of dihydropyridine receptor cDNAs. Nature. 1990 Aug 9;346(6284):569–572. doi: 10.1038/346569a0. [DOI] [PubMed] [Google Scholar]
- Bean B. P., Nowycky M. C., Tsien R. W. Beta-adrenergic modulation of calcium channels in frog ventricular heart cells. 1984 Jan 26-Feb 1Nature. 307(5949):371–375. doi: 10.1038/307371a0. [DOI] [PubMed] [Google Scholar]
- Beurg M., Sukhareva M., Strube C., Powers P. A., Gregg R. G., Coronado R. Recovery of Ca2+ current, charge movements, and Ca2+ transients in myotubes deficient in dihydropyridine receptor beta 1 subunit transfected with beta 1 cDNA. Biophys J. 1997 Aug;73(2):807–818. doi: 10.1016/S0006-3495(97)78113-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bourinet E., Zamponi G. W., Stea A., Soong T. W., Lewis B. A., Jones L. P., Yue D. T., Snutch T. P. The alpha 1E calcium channel exhibits permeation properties similar to low-voltage-activated calcium channels. J Neurosci. 1996 Aug 15;16(16):4983–4993. doi: 10.1523/JNEUROSCI.16-16-04983.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bournaud R., Shimahara T., Garcia L., Rieger F. Appearance of the slow Ca conductance in myotubes from mutant mice with "muscular dysgenesis". Pflugers Arch. 1989 Aug;414(4):410–415. doi: 10.1007/BF00585050. [DOI] [PubMed] [Google Scholar]
- Bulteau L., Cogné M., Cognard C., Raymond G. Reversal of the relative expression of cardiac and skeletal alpha1 subunit isoforms of L-type calcium channel during in vitro myogenesis. Pflugers Arch. 1997 Jan;433(3):376–378. doi: 10.1007/s004240050291. [DOI] [PubMed] [Google Scholar]
- Castellano A., Wei X., Birnbaumer L., Perez-Reyes E. Cloning and expression of a third calcium channel beta subunit. J Biol Chem. 1993 Feb 15;268(5):3450–3455. [PubMed] [Google Scholar]
- Chaudhari N. A single nucleotide deletion in the skeletal muscle-specific calcium channel transcript of muscular dysgenesis (mdg) mice. J Biol Chem. 1992 Dec 25;267(36):25636–25639. [PubMed] [Google Scholar]
- Chaudhari N., Beam K. G. mRNA for cardiac calcium channel is expressed during development of skeletal muscle. Dev Biol. 1993 Feb;155(2):507–515. doi: 10.1006/dbio.1993.1048. [DOI] [PubMed] [Google Scholar]
- Chien A. J., Zhao X., Shirokov R. E., Puri T. S., Chang C. F., Sun D., Rios E., Hosey M. M. Roles of a membrane-localized beta subunit in the formation and targeting of functional L-type Ca2+ channels. J Biol Chem. 1995 Dec 15;270(50):30036–30044. doi: 10.1074/jbc.270.50.30036. [DOI] [PubMed] [Google Scholar]
- Conti F., De Felice L. J., Wanke E. Potassium and sodium ion current noise in the membrane of the squid giant axon. J Physiol. 1975 Jun;248(1):45–82. doi: 10.1113/jphysiol.1975.sp010962. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dirksen R. T., Beam K. G. Single calcium channel behavior in native skeletal muscle. J Gen Physiol. 1995 Feb;105(2):227–247. doi: 10.1085/jgp.105.2.227. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Flucher B. E., Phillips J. L., Powell J. A. Dihydropyridine receptor alpha subunits in normal and dysgenic muscle in vitro: expression of alpha 1 is required for proper targeting and distribution of alpha 2. J Cell Biol. 1991 Dec;115(5):1345–1356. doi: 10.1083/jcb.115.5.1345. [DOI] [PMC free article] [PubMed] [Google Scholar]
- García J., Beam K. G. Measurement of calcium transients and slow calcium current in myotubes. J Gen Physiol. 1994 Jan;103(1):107–123. doi: 10.1085/jgp.103.1.107. [DOI] [PMC free article] [PubMed] [Google Scholar]
- García J., Tanabe T., Beam K. G. Relationship of calcium transients to calcium currents and charge movements in myotubes expressing skeletal and cardiac dihydropyridine receptors. J Gen Physiol. 1994 Jan;103(1):125–147. doi: 10.1085/jgp.103.1.125. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gregg R. G., Messing A., Strube C., Beurg M., Moss R., Behan M., Sukhareva M., Haynes S., Powell J. A., Coronado R. Absence of the beta subunit (cchb1) of the skeletal muscle dihydropyridine receptor alters expression of the alpha 1 subunit and eliminates excitation-contraction coupling. Proc Natl Acad Sci U S A. 1996 Nov 26;93(24):13961–13966. doi: 10.1073/pnas.93.24.13961. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Heinemann S. H., Conti F. Nonstationary noise analysis and application to patch clamp recordings. Methods Enzymol. 1992;207:131–148. doi: 10.1016/0076-6879(92)07009-d. [DOI] [PubMed] [Google Scholar]
- Hullin R., Singer-Lahat D., Freichel M., Biel M., Dascal N., Hofmann F., Flockerzi V. Calcium channel beta subunit heterogeneity: functional expression of cloned cDNA from heart, aorta and brain. EMBO J. 1992 Mar;11(3):885–890. doi: 10.1002/j.1460-2075.1992.tb05126.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Itagaki K., Koch W. J., Bodi I., Klöckner U., Slish D. F., Schwartz A. Native-type DHP-sensitive calcium channel currents are produced by cloned rat aortic smooth muscle and cardiac alpha 1 subunits expressed in Xenopus laevis oocytes and are regulated by alpha 2- and beta-subunits. FEBS Lett. 1992 Feb 10;297(3):221–225. doi: 10.1016/0014-5793(92)80542-o. [DOI] [PubMed] [Google Scholar]
- Kamp T. J., Pérez-García M. T., Marban E. Enhancement of ionic current and charge movement by coexpression of calcium channel beta 1A subunit with alpha 1C subunit in a human embryonic kidney cell line. J Physiol. 1996 Apr 1;492(Pt 1):89–96. doi: 10.1113/jphysiol.1996.sp021291. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Knudson C. M., Chaudhari N., Sharp A. H., Powell J. A., Beam K. G., Campbell K. P. Specific absence of the alpha 1 subunit of the dihydropyridine receptor in mice with muscular dysgenesis. J Biol Chem. 1989 Jan 25;264(3):1345–1348. [PubMed] [Google Scholar]
- Lory P., Varadi G., Schwartz A. The beta subunit controls the gating and dihydropyridine sensitivity of the skeletal muscle Ca2+ channel. Biophys J. 1992 Nov;63(5):1421–1424. doi: 10.1016/S0006-3495(92)81705-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lory P., Varadi G., Slish D. F., Varadi M., Schwartz A. Characterization of beta subunit modulation of a rabbit cardiac L-type Ca2+ channel alpha 1 subunit as expressed in mouse L cells. FEBS Lett. 1993 Jan 4;315(2):167–172. doi: 10.1016/0014-5793(93)81156-t. [DOI] [PubMed] [Google Scholar]
- Neher E., Stevens C. F. Conductance fluctuations and ionic pores in membranes. Annu Rev Biophys Bioeng. 1977;6:345–381. doi: 10.1146/annurev.bb.06.060177.002021. [DOI] [PubMed] [Google Scholar]
- Nishimura S., Takeshima H., Hofmann F., Flockerzi V., Imoto K. Requirement of the calcium channel beta subunit for functional conformation. FEBS Lett. 1993 Jun 21;324(3):283–286. doi: 10.1016/0014-5793(93)80135-h. [DOI] [PubMed] [Google Scholar]
- Noceti F., Baldelli P., Wei X., Qin N., Toro L., Birnbaumer L., Stefani E. Effective gating charges per channel in voltage-dependent K+ and Ca2+ channels. J Gen Physiol. 1996 Sep;108(3):143–155. doi: 10.1085/jgp.108.3.143. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ohlendieck K., Briggs F. N., Lee K. F., Wechsler A. W., Campbell K. P. Analysis of excitation-contraction-coupling components in chronically stimulated canine skeletal muscle. Eur J Biochem. 1991 Dec 18;202(3):739–747. doi: 10.1111/j.1432-1033.1991.tb16428.x. [DOI] [PubMed] [Google Scholar]
- Perez-Reyes E., Castellano A., Kim H. S., Bertrand P., Baggstrom E., Lacerda A. E., Wei X. Y., Birnbaumer L. Cloning and expression of a cardiac/brain beta subunit of the L-type calcium channel. J Biol Chem. 1992 Jan 25;267(3):1792–1797. [PubMed] [Google Scholar]
- Pérez-García M. T., Kamp T. J., Marbán E. Functional properties of cardiac L-type calcium channels transiently expressed in HEK293 cells. Roles of alpha 1 and beta subunits. J Gen Physiol. 1995 Feb;105(2):289–305. doi: 10.1085/jgp.105.2.289. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shimahara T., Bournaud R. Barium currents in developing skeletal muscle cells of normal and mutant mice foetuses with 'muscular dysgenesis'. Cell Calcium. 1991 Nov;12(10):727–733. doi: 10.1016/0143-4160(91)90041-c. [DOI] [PubMed] [Google Scholar]
- Sigworth F. J. The variance of sodium current fluctuations at the node of Ranvier. J Physiol. 1980 Oct;307:97–129. doi: 10.1113/jphysiol.1980.sp013426. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Singer D., Biel M., Lotan I., Flockerzi V., Hofmann F., Dascal N. The roles of the subunits in the function of the calcium channel. Science. 1991 Sep 27;253(5027):1553–1557. doi: 10.1126/science.1716787. [DOI] [PubMed] [Google Scholar]
- Strube C., Beurg M., Powers P. A., Gregg R. G., Coronado R. Reduced Ca2+ current, charge movement, and absence of Ca2+ transients in skeletal muscle deficient in dihydropyridine receptor beta 1 subunit. Biophys J. 1996 Nov;71(5):2531–2543. doi: 10.1016/S0006-3495(96)79446-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tanabe T., Adams B. A., Numa S., Beam K. G. Repeat I of the dihydropyridine receptor is critical in determining calcium channel activation kinetics. Nature. 1991 Aug 29;352(6338):800–803. doi: 10.1038/352800a0. [DOI] [PubMed] [Google Scholar]
- Tanabe T., Beam K. G., Adams B. A., Niidome T., Numa S. Regions of the skeletal muscle dihydropyridine receptor critical for excitation-contraction coupling. Nature. 1990 Aug 9;346(6284):567–569. doi: 10.1038/346567a0. [DOI] [PubMed] [Google Scholar]
- Tanabe T., Beam K. G., Powell J. A., Numa S. Restoration of excitation-contraction coupling and slow calcium current in dysgenic muscle by dihydropyridine receptor complementary DNA. Nature. 1988 Nov 10;336(6195):134–139. doi: 10.1038/336134a0. [DOI] [PubMed] [Google Scholar]
- Tanabe T., Mikami A., Numa S., Beam K. G. Cardiac-type excitation-contraction coupling in dysgenic skeletal muscle injected with cardiac dihydropyridine receptor cDNA. Nature. 1990 Mar 29;344(6265):451–453. doi: 10.1038/344451a0. [DOI] [PubMed] [Google Scholar]
- Tsien R. W., Bean B. P., Hess P., Lansman J. B., Nilius B., Nowycky M. C. Mechanisms of calcium channel modulation by beta-adrenergic agents and dihydropyridine calcium agonists. J Mol Cell Cardiol. 1986 Jul;18(7):691–710. doi: 10.1016/s0022-2828(86)80941-5. [DOI] [PubMed] [Google Scholar]
- Varadi G., Lory P., Schultz D., Varadi M., Schwartz A. Acceleration of activation and inactivation by the beta subunit of the skeletal muscle calcium channel. Nature. 1991 Jul 11;352(6331):159–162. doi: 10.1038/352159a0. [DOI] [PubMed] [Google Scholar]
- Varadi G., Mikala G., Lory P., Varadi M., Drouet B., Pinçon-Raymond M., Schwartz A. Endogenous cardiac Ca2+ channels do not overcome the E-C coupling defect in immortalized dysgenic muscle cells: evidence for a missing link. FEBS Lett. 1995 Jul 24;368(3):405–410. doi: 10.1016/0014-5793(95)00697-8. [DOI] [PubMed] [Google Scholar]
- Wei X. Y., Perez-Reyes E., Lacerda A. E., Schuster G., Brown A. M., Birnbaumer L. Heterologous regulation of the cardiac Ca2+ channel alpha 1 subunit by skeletal muscle beta and gamma subunits. Implications for the structure of cardiac L-type Ca2+ channels. J Biol Chem. 1991 Nov 15;266(32):21943–21947. [PubMed] [Google Scholar]
- Yang J., Ellinor P. T., Sather W. A., Zhang J. F., Tsien R. W. Molecular determinants of Ca2+ selectivity and ion permeation in L-type Ca2+ channels. Nature. 1993 Nov 11;366(6451):158–161. doi: 10.1038/366158a0. [DOI] [PubMed] [Google Scholar]