Skip to main content
Molecular Biology of the Cell logoLink to Molecular Biology of the Cell
. 1994 Apr;5(4):485–496. doi: 10.1091/mbc.5.4.485

An insulin-sensitive cation channel controls [Na+]i via [Ca2+]o-regulated Na+ and Ca2+ entry.

J E McGeoch 1, A D Morielli 1
PMCID: PMC301057  PMID: 8054688

Abstract

The insulin-stimulated cation channel previously identified in patch-clamped muscle preparations is here shown to be responsible for bulk Na+ entry into the cell. The mainly Na+ current of the channel was shown to be accompanied by an inhibitory Ca2+ component responsible for oscillations. Here, using quantitative fluorescence imaging of Fura-2- and SBFI-loaded soleus muscle, we measure changes in [Na+]i and [Ca2+]i related to channel function. Insulin increased [Na+]i and [Ca+]i in a transient spike of < 1-min duration. There was a momentary dip in [Na+]i related to inhibition of the channel by the Ca2+ spike, and changes in external Ca2+ were shown to alter [Na+]i via the cation channel, all effects being blocked by the specific channel inhibitor mu-conotoxin, but not by tetrodotoxin. The [Ca2+]i spike could also be induced by 8-bromo cyclic-guanosine 5'-monophosphate, an analogue of the channel-activator cyclic-guanosine 5'-monophosphate (cGMP). In addition it was noted that insulin reduced the [Ca2+]i rise upon subsequent muscle depolarization by a factor of 3.5. Insulin could be substituted with phorbol ester for the same effect and HA1004, a protein kinase inhibitor, blocked the reduction.

Full text

PDF
485

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Blackshear P. J., Haupt D. M., Stumpo D. J. Insulin activation of protein kinase C: a reassessment. J Biol Chem. 1991 Jun 15;266(17):10946–10952. [PubMed] [Google Scholar]
  2. Boulton T. G., Nye S. H., Robbins D. J., Ip N. Y., Radziejewska E., Morgenbesser S. D., DePinho R. A., Panayotatos N., Cobb M. H., Yancopoulos G. D. ERKs: a family of protein-serine/threonine kinases that are activated and tyrosine phosphorylated in response to insulin and NGF. Cell. 1991 May 17;65(4):663–675. doi: 10.1016/0092-8674(91)90098-j. [DOI] [PubMed] [Google Scholar]
  3. Catterall W. A. Molecular properties of voltage-sensitive sodium channels. Annu Rev Biochem. 1986;55:953–985. doi: 10.1146/annurev.bi.55.070186.004513. [DOI] [PubMed] [Google Scholar]
  4. Chang C. F., Gutierrez L. M., Mundina-Weilenmann C., Hosey M. M. Dihydropyridine-sensitive calcium channels from skeletal muscle. II. Functional effects of differential phosphorylation of channel subunits. J Biol Chem. 1991 Sep 5;266(25):16395–16400. [PubMed] [Google Scholar]
  5. Clausen T., Flatman J. A. Effects of insulin and epinephrine on Na+-K+ and glucose transport in soleus muscle. Am J Physiol. 1987 Apr;252(4 Pt 1):E492–E499. doi: 10.1152/ajpendo.1987.252.4.E492. [DOI] [PubMed] [Google Scholar]
  6. Cooper D. R., Ishizuka T., Watson J. E., Standaert M. L., Nair G., Farese R. V. Protein kinase C activation patterns are determined by methodological variations. Studies of insulin action in BC3H-1 myocytes and rat adipose tissue. Biochim Biophys Acta. 1990 Aug 13;1054(1):95–102. doi: 10.1016/0167-4889(90)90210-5. [DOI] [PubMed] [Google Scholar]
  7. Cruz L. J., Gray W. R., Olivera B. M., Zeikus R. D., Kerr L., Yoshikami D., Moczydlowski E. Conus geographus toxins that discriminate between neuronal and muscle sodium channels. J Biol Chem. 1985 Aug 5;260(16):9280–9288. [PubMed] [Google Scholar]
  8. Dhallan R. S., Yau K. W., Schrader K. A., Reed R. R. Primary structure and functional expression of a cyclic nucleotide-activated channel from olfactory neurons. Nature. 1990 Sep 13;347(6289):184–187. doi: 10.1038/347184a0. [DOI] [PubMed] [Google Scholar]
  9. Ebashi S. Excitation-contraction coupling and the mechanism of muscle contraction. Annu Rev Physiol. 1991;53:1–16. doi: 10.1146/annurev.ph.53.030191.000245. [DOI] [PubMed] [Google Scholar]
  10. Grynkiewicz G., Poenie M., Tsien R. Y. A new generation of Ca2+ indicators with greatly improved fluorescence properties. J Biol Chem. 1985 Mar 25;260(6):3440–3450. [PubMed] [Google Scholar]
  11. Haas M. Properties and diversity of (Na-K-Cl) cotransporters. Annu Rev Physiol. 1989;51:443–457. doi: 10.1146/annurev.ph.51.030189.002303. [DOI] [PubMed] [Google Scholar]
  12. Harootunian A. T., Kao J. P., Eckert B. K., Tsien R. Y. Fluorescence ratio imaging of cytosolic free Na+ in individual fibroblasts and lymphocytes. J Biol Chem. 1989 Nov 15;264(32):19458–19467. [PubMed] [Google Scholar]
  13. Hei Y. J., McNeill J. H., Sanghera J. S., Diamond J., Bryer-Ash M., Pelech S. L. Characterization of insulin-stimulated seryl/threonyl protein kinases in rat skeletal muscle. J Biol Chem. 1993 Jun 25;268(18):13203–13213. [PubMed] [Google Scholar]
  14. Hidaka H., Inagaki M., Kawamoto S., Sasaki Y. Isoquinolinesulfonamides, novel and potent inhibitors of cyclic nucleotide dependent protein kinase and protein kinase C. Biochemistry. 1984 Oct 9;23(21):5036–5041. doi: 10.1021/bi00316a032. [DOI] [PubMed] [Google Scholar]
  15. Hsu Y. M., Guidotti G. Effects of hypokalemia on the properties and expression of the (Na+,K+)-ATPase of rat skeletal muscle. J Biol Chem. 1991 Jan 5;266(1):427–433. [PubMed] [Google Scholar]
  16. Jan L. Y., Jan Y. N. A superfamily of ion channels. Nature. 1990 Jun 21;345(6277):672–672. doi: 10.1038/345672a0. [DOI] [PubMed] [Google Scholar]
  17. Kawamura S., Murakami M. Calcium-dependent regulation of cyclic GMP phosphodiesterase by a protein from frog retinal rods. Nature. 1991 Jan 31;349(6308):420–423. doi: 10.1038/349420a0. [DOI] [PubMed] [Google Scholar]
  18. Koch K. W., Stryer L. Highly cooperative feedback control of retinal rod guanylate cyclase by calcium ions. Nature. 1988 Jul 7;334(6177):64–66. doi: 10.1038/334064a0. [DOI] [PubMed] [Google Scholar]
  19. Kyriakis J. M., App H., Zhang X. F., Banerjee P., Brautigan D. L., Rapp U. R., Avruch J. Raf-1 activates MAP kinase-kinase. Nature. 1992 Jul 30;358(6385):417–421. doi: 10.1038/358417a0. [DOI] [PubMed] [Google Scholar]
  20. Lavoinne A., Erikson E., Maller J. L., Price D. J., Avruch J., Cohen P. Purification and characterisation of the insulin-stimulated protein kinase from rabbit skeletal muscle; close similarity to S6 kinase II. Eur J Biochem. 1991 Aug 1;199(3):723–728. doi: 10.1111/j.1432-1033.1991.tb16176.x. [DOI] [PubMed] [Google Scholar]
  21. Lytton J., Westlin M., Hanley M. R. Thapsigargin inhibits the sarcoplasmic or endoplasmic reticulum Ca-ATPase family of calcium pumps. J Biol Chem. 1991 Sep 15;266(26):17067–17071. [PubMed] [Google Scholar]
  22. McGeoch J. E., Guidotti G. An insulin-stimulated cation channel in skeletal muscle. Inhibition by calcium causes oscillation. J Biol Chem. 1992 Jan 15;267(2):832–841. [PubMed] [Google Scholar]
  23. McGeoch M. W., McGeoch J. E. Power spectra and cooperativity of a calcium-regulated cation channel. Biophys J. 1994 Jan;66(1):161–168. doi: 10.1016/S0006-3495(94)80747-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. McGill D. L. Characterization of the adipocyte ghost (Na+,K+) pump. Insights into the insulin regulation of the adipocyte (Na+,K+) pump. J Biol Chem. 1991 Aug 25;266(24):15817–15823. [PubMed] [Google Scholar]
  25. Minta A., Tsien R. Y. Fluorescent indicators for cytosolic sodium. J Biol Chem. 1989 Nov 15;264(32):19449–19457. [PubMed] [Google Scholar]
  26. Negulescu P. A., Harootunian A., Tsien R. Y., Machen T. E. Fluorescence measurements of cytosolic free Na concentration, influx and efflux in gastric cells. Cell Regul. 1990 Feb;1(3):259–268. doi: 10.1091/mbc.1.3.259. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Nishimoto I., Ohkuni Y., Ogata E., Kojima I. Insulin-like growth factor II increases cytoplasmic free calcium in competent Balb/c 3T3 cells treated with epidermal growth factor. Biochem Biophys Res Commun. 1987 Jan 15;142(1):275–286. doi: 10.1016/0006-291x(87)90481-5. [DOI] [PubMed] [Google Scholar]
  28. Nishizuka Y. The molecular heterogeneity of protein kinase C and its implications for cellular regulation. Nature. 1988 Aug 25;334(6184):661–665. doi: 10.1038/334661a0. [DOI] [PubMed] [Google Scholar]
  29. Penner R., Matthews G., Neher E. Regulation of calcium influx by second messengers in rat mast cells. Nature. 1988 Aug 11;334(6182):499–504. doi: 10.1038/334499a0. [DOI] [PubMed] [Google Scholar]
  30. Resh M. D., Nemenoff R. A., Guidotti G. Insulin stimulation of (Na+,K+)-adenosine triphosphatase-dependent 86Rb+ uptake in rat adipocytes. J Biol Chem. 1980 Nov 25;255(22):10938–10945. [PubMed] [Google Scholar]
  31. Robbins D. J., Cobb M. H. Extracellular signal-regulated kinases 2 autophosphorylates on a subset of peptides phosphorylated in intact cells in response to insulin and nerve growth factor: analysis by peptide mapping. Mol Biol Cell. 1992 Mar;3(3):299–308. doi: 10.1091/mbc.3.3.299. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Satoh H., Hayashi H., Noda N., Terada H., Kobayashi A., Yamashita Y., Kawai T., Hirano M., Yamazaki N. Quantification of intracellular free sodium ions by using a new fluorescent indicator, sodium-binding benzofuran isophthalate in guinea pig myocytes. Biochem Biophys Res Commun. 1991 Mar 15;175(2):611–616. doi: 10.1016/0006-291x(91)91609-g. [DOI] [PubMed] [Google Scholar]
  33. Standley P. R., Zhang F., Ram J. L., Zemel M. B., Sowers J. R. Insulin attenuates vasopressin-induced calcium transients and a voltage-dependent calcium response in rat vascular smooth muscle cells. J Clin Invest. 1991 Oct;88(4):1230–1236. doi: 10.1172/JCI115426. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Stern J. H., Kaupp U. B., MacLeish P. R. Control of the light-regulated current in rod photoreceptors by cyclic GMP, calcium, and l-cis-diltiazem. Proc Natl Acad Sci U S A. 1986 Feb;83(4):1163–1167. doi: 10.1073/pnas.83.4.1163. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Thastrup O., Cullen P. J., Drøbak B. K., Hanley M. R., Dawson A. P. Thapsigargin, a tumor promoter, discharges intracellular Ca2+ stores by specific inhibition of the endoplasmic reticulum Ca2(+)-ATPase. Proc Natl Acad Sci U S A. 1990 Apr;87(7):2466–2470. doi: 10.1073/pnas.87.7.2466. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Trimmer J. S., Agnew W. S. Molecular diversity of voltage-sensitive Na channels. Annu Rev Physiol. 1989;51:401–418. doi: 10.1146/annurev.ph.51.030189.002153. [DOI] [PubMed] [Google Scholar]
  37. Wong M. M., Foskett J. K. Oscillations of cytosolic sodium during calcium oscillations in exocrine acinar cells. Science. 1991 Nov 15;254(5034):1014–1016. doi: 10.1126/science.1948071. [DOI] [PubMed] [Google Scholar]
  38. Yau K. W., Baylor D. A. Cyclic GMP-activated conductance of retinal photoreceptor cells. Annu Rev Neurosci. 1989;12:289–327. doi: 10.1146/annurev.ne.12.030189.001445. [DOI] [PubMed] [Google Scholar]
  39. Zufall F., Shepherd G. M., Firestein S. Inhibition of the olfactory cyclic nucleotide gated ion channel by intracellular calcium. Proc Biol Sci. 1991 Dec 23;246(1317):225–230. doi: 10.1098/rspb.1991.0148. [DOI] [PubMed] [Google Scholar]

Articles from Molecular Biology of the Cell are provided here courtesy of American Society for Cell Biology

RESOURCES