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. 1998 Aug 17;17(16):4723–4734. doi: 10.1093/emboj/17.16.4723

Constitutive activation of delayed-rectifier potassium channels by a src family tyrosine kinase in Schwann cells.

A Sobko 1, A Peretz 1, B Attali 1
PMCID: PMC1170801  PMID: 9707431

Abstract

In the nervous system, Src family tyrosine kinases are thought to be involved in cell growth, migration, differentiation, apoptosis, as well as in myelination and synaptic plasticity. Emerging evidence indicates that K+ channels are crucial targets of Src tyrosine kinases. However, most of the data accumulated so far refer to heterologous expression, and native K+-channel substrates of Src or Fyn in neurons and glia remain to be elucidated. The present study shows that a Src family tyrosine kinase constitutively activates delayed-rectifier K+ channels (IK) in mouse Schwann cells (SCs). IK currents are markedly downregulated upon exposure of cells to the tyrosine kinase inhibitors herbimycin A and genistein, while a potent upregulation of IK is observed when recombinant Fyn kinase is introduced through the patch pipette. The Kv1.5 and Kv2.1 K+-channel alpha subunits are constitutively tyrosine phosphorylated and physically associate with Fyn both in cultured SCs and in the sciatic nerve in vivo. Kv2.1- channel subunits are found to interact with the Fyn SH2 domain. Inhibition of Schwann cell proliferation by herbimycin A and by K+-channel blockers suggests that the functional linkage between Src tyrosine kinases and IK channels could be important for Schwann cell proliferation and the onset of myelination.

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Selected References

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  1. Amédée T., Ellie E., Dupouy B., Vincent J. D. Voltage-dependent calcium and potassium channels in Schwann cells cultured from dorsal root ganglia of the mouse. J Physiol. 1991 Sep;441:35–56. doi: 10.1113/jphysiol.1991.sp018737. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Atkinson E. A., Ostergaard H., Kane K., Pinkoski M. J., Caputo A., Olszowy M. W., Bleackley R. C. A physical interaction between the cell death protein Fas and the tyrosine kinase p59fynT. J Biol Chem. 1996 Mar 15;271(11):5968–5971. doi: 10.1074/jbc.271.11.5968. [DOI] [PubMed] [Google Scholar]
  3. Attali B., Wang N., Kolot A., Sobko A., Cherepanov V., Soliven B. Characterization of delayed rectifier Kv channels in oligodendrocytes and progenitor cells. J Neurosci. 1997 Nov 1;17(21):8234–8245. doi: 10.1523/JNEUROSCI.17-21-08234.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bare D. J., Lauder J. M., Wilkie M. B., Maness P. F. p59fyn in rat brain is localized in developing axonal tracts and subpopulations of adult neurons and glia. Oncogene. 1993 Jun;8(6):1429–1436. [PubMed] [Google Scholar]
  5. Barres B. A., Chun L. L., Corey D. P. Ion channels in vertebrate glia. Annu Rev Neurosci. 1990;13:441–474. doi: 10.1146/annurev.ne.13.030190.002301. [DOI] [PubMed] [Google Scholar]
  6. Bekele-Arcuri Z., Matos M. F., Manganas L., Strassle B. W., Monaghan M. M., Rhodes K. J., Trimmer J. S. Generation and characterization of subtype-specific monoclonal antibodies to K+ channel alpha- and beta-subunit polypeptides. Neuropharmacology. 1996;35(7):851–865. doi: 10.1016/0028-3908(96)00128-1. [DOI] [PubMed] [Google Scholar]
  7. Bolen J. B. Nonreceptor tyrosine protein kinases. Oncogene. 1993 Aug;8(8):2025–2031. [PubMed] [Google Scholar]
  8. Bowlby M. R., Fadool D. A., Holmes T. C., Levitan I. B. Modulation of the Kv1.3 potassium channel by receptor tyrosine kinases. J Gen Physiol. 1997 Nov;110(5):601–610. doi: 10.1085/jgp.110.5.601. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Boxall A. R., Lancaster B. Tyrosine kinases and synaptic transmission. Eur J Neurosci. 1998 Jan;10(1):2–7. doi: 10.1046/j.1460-9568.1998.00009.x. [DOI] [PubMed] [Google Scholar]
  10. Brockes J. P., Fields K. L., Raff M. C. Studies on cultured rat Schwann cells. I. Establishment of purified populations from cultures of peripheral nerve. Brain Res. 1979 Apr 6;165(1):105–118. doi: 10.1016/0006-8993(79)90048-9. [DOI] [PubMed] [Google Scholar]
  11. Cantley L. C., Songyang Z. Specificity in protein-tyrosine kinase signaling. Adv Second Messenger Phosphoprotein Res. 1997;31:41–48. doi: 10.1016/s1040-7952(97)80007-9. [DOI] [PubMed] [Google Scholar]
  12. Chiu S. Y. Functions and distribution of voltage-gated sodium and potassium channels in mammalian Schwann cells. Glia. 1991;4(6):541–558. doi: 10.1002/glia.440040602. [DOI] [PubMed] [Google Scholar]
  13. Chiu S. Y., Scherer S. S., Blonski M., Kang S. S., Messing A. Axons regulate the expression of Shaker-like potassium channel genes in Schwann cells in peripheral nerve. Glia. 1994 Sep;12(1):1–11. doi: 10.1002/glia.440120102. [DOI] [PubMed] [Google Scholar]
  14. Chiu S. Y., Wilson G. F. The role of potassium channels in Schwann cell proliferation in Wallerian degeneration of explant rabbit sciatic nerves. J Physiol. 1989 Jan;408:199–222. doi: 10.1113/jphysiol.1989.sp017455. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Courtneidge S. A., Fumagalli S. A mitotic function for Src? Trends Cell Biol. 1994 Oct;4(10):345–347. doi: 10.1016/0962-8924(94)90074-4. [DOI] [PubMed] [Google Scholar]
  16. Du J., Zhang L., Weiser M., Rudy B., McBain C. J. Developmental expression and functional characterization of the potassium-channel subunit Kv3.1b in parvalbumin-containing interneurons of the rat hippocampus. J Neurosci. 1996 Jan 15;16(2):506–518. doi: 10.1523/JNEUROSCI.16-02-00506.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Erpel T., Courtneidge S. A. Src family protein tyrosine kinases and cellular signal transduction pathways. Curr Opin Cell Biol. 1995 Apr;7(2):176–182. doi: 10.1016/0955-0674(95)80025-5. [DOI] [PubMed] [Google Scholar]
  18. Fadool D. A., Holmes T. C., Berman K., Dagan D., Levitan I. B. Tyrosine phosphorylation modulates current amplitude and kinetics of a neuronal voltage-gated potassium channel. J Neurophysiol. 1997 Sep;78(3):1563–1573. doi: 10.1152/jn.1997.78.3.1563. [DOI] [PubMed] [Google Scholar]
  19. Fink M., Duprat F., Lesage F., Heurteaux C., Romey G., Barhanin J., Lazdunski M. A new K+ channel beta subunit to specifically enhance Kv2.2 (CDRK) expression. J Biol Chem. 1996 Oct 18;271(42):26341–26348. doi: 10.1074/jbc.271.42.26341. [DOI] [PubMed] [Google Scholar]
  20. Frech G. C., VanDongen A. M., Schuster G., Brown A. M., Joho R. H. A novel potassium channel with delayed rectifier properties isolated from rat brain by expression cloning. Nature. 1989 Aug 24;340(6235):642–645. doi: 10.1038/340642a0. [DOI] [PubMed] [Google Scholar]
  21. Fuhrer C., Sugiyama J. E., Taylor R. G., Hall Z. W. Association of muscle-specific kinase MuSK with the acetylcholine receptor in mammalian muscle. EMBO J. 1997 Aug 15;16(16):4951–4960. doi: 10.1093/emboj/16.16.4951. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Grant S. G., O'Dell T. J., Karl K. A., Stein P. L., Soriano P., Kandel E. R. Impaired long-term potentiation, spatial learning, and hippocampal development in fyn mutant mice. Science. 1992 Dec 18;258(5090):1903–1910. doi: 10.1126/science.1361685. [DOI] [PubMed] [Google Scholar]
  23. Grinspan J. B., Marchionni M. A., Reeves M., Coulaloglou M., Scherer S. S. Axonal interactions regulate Schwann cell apoptosis in developing peripheral nerve: neuregulin receptors and the role of neuregulins. J Neurosci. 1996 Oct 1;16(19):6107–6118. doi: 10.1523/JNEUROSCI.16-19-06107.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Hamill O. P., Marty A., Neher E., Sakmann B., Sigworth F. J. Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches. Pflugers Arch. 1981 Aug;391(2):85–100. doi: 10.1007/BF00656997. [DOI] [PubMed] [Google Scholar]
  25. Holmes T. C., Fadool D. A., Levitan I. B. Tyrosine phosphorylation of the Kv1.3 potassium channel. J Neurosci. 1996 Mar 1;16(5):1581–1590. doi: 10.1523/JNEUROSCI.16-05-01581.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Holmes T. C., Fadool D. A., Ren R., Levitan I. B. Association of Src tyrosine kinase with a human potassium channel mediated by SH3 domain. Science. 1996 Dec 20;274(5295):2089–2091. doi: 10.1126/science.274.5295.2089. [DOI] [PubMed] [Google Scholar]
  27. Hoppe D., Lux H. D., Schachner M., Kettenmann H. Activation of K+ currents in cultured Schwann cells is controlled by extracellular pH. Pflugers Arch. 1989 Oct;415(1):22–28. doi: 10.1007/BF00373137. [DOI] [PubMed] [Google Scholar]
  28. Huang X. Y., Morielli A. D., Peralta E. G. Tyrosine kinase-dependent suppression of a potassium channel by the G protein-coupled m1 muscarinic acetylcholine receptor. Cell. 1993 Dec 17;75(6):1145–1156. doi: 10.1016/0092-8674(93)90324-j. [DOI] [PubMed] [Google Scholar]
  29. Hugnot J. P., Salinas M., Lesage F., Guillemare E., de Weille J., Heurteaux C., Mattéi M. G., Lazdunski M. Kv8.1, a new neuronal potassium channel subunit with specific inhibitory properties towards Shab and Shaw channels. EMBO J. 1996 Jul 1;15(13):3322–3331. [PMC free article] [PubMed] [Google Scholar]
  30. Jessen K. R., Brennan A., Morgan L., Mirsky R., Kent A., Hashimoto Y., Gavrilovic J. The Schwann cell precursor and its fate: a study of cell death and differentiation during gliogenesis in rat embryonic nerves. Neuron. 1994 Mar;12(3):509–527. doi: 10.1016/0896-6273(94)90209-7. [DOI] [PubMed] [Google Scholar]
  31. Jonas E. A., Kaczmarek L. K. Regulation of potassium channels by protein kinases. Curr Opin Neurobiol. 1996 Jun;6(3):318–323. doi: 10.1016/s0959-4388(96)80114-0. [DOI] [PubMed] [Google Scholar]
  32. Jonas E. A., Knox R. J., Kaczmarek L. K., Schwartz J. H., Solomon D. H. Insulin receptor in Aplysia neurons: characterization, molecular cloning, and modulation of ion currents. J Neurosci. 1996 Mar 1;16(5):1645–1658. doi: 10.1523/JNEUROSCI.16-05-01645.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Konishi T. Voltage-dependent potassium channels in mouse Schwann cells. J Physiol. 1989 Apr;411:115–130. doi: 10.1113/jphysiol.1989.sp017564. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Köhr G., Seeburg P. H. Subtype-specific regulation of recombinant NMDA receptor-channels by protein tyrosine kinases of the src family. J Physiol. 1996 Apr 15;492(Pt 2):445–452. doi: 10.1113/jphysiol.1996.sp021320. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  36. Le Beau J. M., Tedeschi B., Walter G. Increased expression of pp60c-src protein-tyrosine kinase during peripheral nerve regeneration. J Neurosci Res. 1991 Feb;28(2):299–309. doi: 10.1002/jnr.490280217. [DOI] [PubMed] [Google Scholar]
  37. Lev S., Moreno H., Martinez R., Canoll P., Peles E., Musacchio J. M., Plowman G. D., Rudy B., Schlessinger J. Protein tyrosine kinase PYK2 involved in Ca(2+)-induced regulation of ion channel and MAP kinase functions. Nature. 1995 Aug 31;376(6543):737–745. doi: 10.1038/376737a0. [DOI] [PubMed] [Google Scholar]
  38. Maletic-Savatic M., Lenn N. J., Trimmer J. S. Differential spatiotemporal expression of K+ channel polypeptides in rat hippocampal neurons developing in situ and in vitro. J Neurosci. 1995 May;15(5 Pt 2):3840–3851. doi: 10.1523/JNEUROSCI.15-05-03840.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Mi H., Deerinck T. J., Ellisman M. H., Schwarz T. L. Differential distribution of closely related potassium channels in rat Schwann cells. J Neurosci. 1995 May;15(5 Pt 2):3761–3774. doi: 10.1523/JNEUROSCI.15-05-03761.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Migita K., Eguchi K., Kawabe Y., Nagataki S. Tyrosine phosphorylation participates in peripheral T-cell activation and programmed cell death in vivo. Immunology. 1995 Aug;85(4):550–555. [PMC free article] [PubMed] [Google Scholar]
  41. Mirsky R., Jessen K. R. Schwann cell development, differentiation and myelination. Curr Opin Neurobiol. 1996 Feb;6(1):89–96. doi: 10.1016/s0959-4388(96)80013-4. [DOI] [PubMed] [Google Scholar]
  42. Moarefi I., LaFevre-Bernt M., Sicheri F., Huse M., Lee C. H., Kuriyan J., Miller W. T. Activation of the Src-family tyrosine kinase Hck by SH3 domain displacement. Nature. 1997 Feb 13;385(6617):650–653. doi: 10.1038/385650a0. [DOI] [PubMed] [Google Scholar]
  43. Pappas C. A., Ritchie J. M. Effect of specific ion channel blockers on cultured Schwann cell proliferation. Glia. 1998 Feb;22(2):113–120. [PubMed] [Google Scholar]
  44. Pappas C. A., Ullrich N., Sontheimer H. Reduction of glial proliferation by K+ channel blockers is mediated by changes in pHi. Neuroreport. 1994 Dec 30;6(1):193–196. doi: 10.1097/00001756-199412300-00049. [DOI] [PubMed] [Google Scholar]
  45. Patel A. J., Lazdunski M., Honoré E. Kv2.1/Kv9.3, a novel ATP-dependent delayed-rectifier K+ channel in oxygen-sensitive pulmonary artery myocytes. EMBO J. 1997 Nov 17;16(22):6615–6625. doi: 10.1093/emboj/16.22.6615. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Prevarskaya N. B., Skryma R. N., Vacher P., Daniel N., Djiane J., Dufy B. Role of tyrosine phosphorylation in potassium channel activation. Functional association with prolactin receptor and JAK2 tyrosine kinase. J Biol Chem. 1995 Oct 13;270(41):24292–24299. doi: 10.1074/jbc.270.41.24292. [DOI] [PubMed] [Google Scholar]
  47. Qian D., Lev S., van Oers N. S., Dikic I., Schlessinger J., Weiss A. Tyrosine phosphorylation of Pyk2 is selectively regulated by Fyn during TCR signaling. J Exp Med. 1997 Apr 7;185(7):1253–1259. doi: 10.1084/jem.185.7.1253. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Ritchie J. M. Voltage-gated ion channels in Schwann cells and glia. Trends Neurosci. 1992 Sep;15(9):345–351. doi: 10.1016/0166-2236(92)90052-a. [DOI] [PubMed] [Google Scholar]
  49. Roche S., Fumagalli S., Courtneidge S. A. Requirement for Src family protein tyrosine kinases in G2 for fibroblast cell division. Science. 1995 Sep 15;269(5230):1567–1569. doi: 10.1126/science.7545311. [DOI] [PubMed] [Google Scholar]
  50. Ross C. A., Wright G. E., Resh M. D., Pearson R. C., Snyder S. H. Brain-specific src oncogene mRNA mapped in rat brain by in situ hybridization. Proc Natl Acad Sci U S A. 1988 Dec;85(24):9831–9835. doi: 10.1073/pnas.85.24.9831. [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. Salinas M., Duprat F., Heurteaux C., Hugnot J. P., Lazdunski M. New modulatory alpha subunits for mammalian Shab K+ channels. J Biol Chem. 1997 Sep 26;272(39):24371–24379. doi: 10.1074/jbc.272.39.24371. [DOI] [PubMed] [Google Scholar]
  52. Salinas M., de Weille J., Guillemare E., Lazdunski M., Hugnot J. P. Modes of regulation of shab K+ channel activity by the Kv8.1 subunit. J Biol Chem. 1997 Mar 28;272(13):8774–8780. doi: 10.1074/jbc.272.13.8774. [DOI] [PubMed] [Google Scholar]
  53. Songyang Z., Carraway K. L., 3rd, Eck M. J., Harrison S. C., Feldman R. A., Mohammadi M., Schlessinger J., Hubbard S. R., Smith D. P., Eng C. Catalytic specificity of protein-tyrosine kinases is critical for selective signalling. Nature. 1995 Feb 9;373(6514):536–539. doi: 10.1038/373536a0. [DOI] [PubMed] [Google Scholar]
  54. Songyang Z., Shoelson S. E., Chaudhuri M., Gish G., Pawson T., Haser W. G., King F., Roberts T., Ratnofsky S., Lechleider R. J. SH2 domains recognize specific phosphopeptide sequences. Cell. 1993 Mar 12;72(5):767–778. doi: 10.1016/0092-8674(93)90404-e. [DOI] [PubMed] [Google Scholar]
  55. Sontheimer H. Voltage-dependent ion channels in glial cells. Glia. 1994 Jun;11(2):156–172. doi: 10.1002/glia.440110210. [DOI] [PubMed] [Google Scholar]
  56. Stewart H. J., Bradke F., Tabernero A., Morrell D., Jessen K. R., Mirsky R. Regulation of rat Schwann cell Po expression and DNA synthesis by insulin-like growth factors in vitro. Eur J Neurosci. 1996 Mar;8(3):553–564. doi: 10.1111/j.1460-9568.1996.tb01240.x. [DOI] [PubMed] [Google Scholar]
  57. Swope S. L., Huganir R. L. Binding of the nicotinic acetylcholine receptor to SH2 domains of Fyn and Fyk protein tyrosine kinases. J Biol Chem. 1994 Nov 25;269(47):29817–29824. [PubMed] [Google Scholar]
  58. Syroid D. E., Maycox P. R., Burrola P. G., Liu N., Wen D., Lee K. F., Lemke G., Kilpatrick T. J. Cell death in the Schwann cell lineage and its regulation by neuregulin. Proc Natl Acad Sci U S A. 1996 Aug 20;93(17):9229–9234. doi: 10.1073/pnas.93.17.9229. [DOI] [PMC free article] [PubMed] [Google Scholar]
  59. Szabò I., Gulbins E., Apfel H., Zhang X., Barth P., Busch A. E., Schlottmann K., Pongs O., Lang F. Tyrosine phosphorylation-dependent suppression of a voltage-gated K+ channel in T lymphocytes upon Fas stimulation. J Biol Chem. 1996 Aug 23;271(34):20465–20469. doi: 10.1074/jbc.271.34.20465. [DOI] [PubMed] [Google Scholar]
  60. Thomas S. M., Brugge J. S. Cellular functions regulated by Src family kinases. Annu Rev Cell Dev Biol. 1997;13:513–609. doi: 10.1146/annurev.cellbio.13.1.513. [DOI] [PubMed] [Google Scholar]
  61. Trachtenberg J. T., Thompson W. J. Schwann cell apoptosis at developing neuromuscular junctions is regulated by glial growth factor. Nature. 1996 Jan 11;379(6561):174–177. doi: 10.1038/379174a0. [DOI] [PubMed] [Google Scholar]
  62. Trotter J., Boulter C. A., Sontheimer H., Schachner M., Wagner E. F. Expression of v-src arrests murine glial cell differentiation. Oncogene. 1989 Apr;4(4):457–464. [PubMed] [Google Scholar]
  63. Tsai W., Morielli A. D., Peralta E. G. The m1 muscarinic acetylcholine receptor transactivates the EGF receptor to modulate ion channel activity. EMBO J. 1997 Aug 1;16(15):4597–4605. doi: 10.1093/emboj/16.15.4597. [DOI] [PMC free article] [PubMed] [Google Scholar]
  64. Umemori H., Sato S., Yagi T., Aizawa S., Yamamoto T. Initial events of myelination involve Fyn tyrosine kinase signalling. Nature. 1994 Feb 10;367(6463):572–576. doi: 10.1038/367572a0. [DOI] [PubMed] [Google Scholar]
  65. Umemori H., Wanaka A., Kato H., Takeuchi M., Tohyama M., Yamamoto T. Specific expressions of Fyn and Lyn, lymphocyte antigen receptor-associated tyrosine kinases, in the central nervous system. Brain Res Mol Brain Res. 1992 Dec;16(3-4):303–310. doi: 10.1016/0169-328x(92)90239-8. [DOI] [PubMed] [Google Scholar]
  66. Wilson G. F., Chiu S. Y. Mitogenic factors regulate ion channels in Schwann cells cultured from newborn rat sciatic nerve. J Physiol. 1993 Oct;470:501–520. doi: 10.1113/jphysiol.1993.sp019872. [DOI] [PMC free article] [PubMed] [Google Scholar]
  67. Wilson G. F., Chiu S. Y. Potassium channel regulation in Schwann cells during early developmental myelinogenesis. J Neurosci. 1990 May;10(5):1615–1625. doi: 10.1523/JNEUROSCI.10-05-01615.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  68. Yu S. P., Yeh C. H., Sensi S. L., Gwag B. J., Canzoniero L. M., Farhangrazi Z. S., Ying H. S., Tian M., Dugan L. L., Choi D. W. Mediation of neuronal apoptosis by enhancement of outward potassium current. Science. 1997 Oct 3;278(5335):114–117. doi: 10.1126/science.278.5335.114. [DOI] [PubMed] [Google Scholar]
  69. Yu X. M., Askalan R., Keil G. J., 2nd, Salter M. W. NMDA channel regulation by channel-associated protein tyrosine kinase Src. Science. 1997 Jan 31;275(5300):674–678. doi: 10.1126/science.275.5300.674. [DOI] [PubMed] [Google Scholar]
  70. Zorick T. S., Lemke G. Schwann cell differentiation. Curr Opin Cell Biol. 1996 Dec;8(6):870–876. doi: 10.1016/s0955-0674(96)80090-1. [DOI] [PubMed] [Google Scholar]

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