Characterization of Intermediate Conductance $K^+$ Channels in Submandibular Gland Acinar Cells

  • Cho, Sung-Man (Department of Physiology, College of Dentistry, Seoul National University and Dental Research Institute) ;
  • Piao, Zheng-Gen (Department of Physiology, College of Dentistry, Seoul National University and Dental Research Institute) ;
  • Kim, Yoon-Bae (Department of Physiology, College of Dentistry, Seoul National University and Dental Research Institute) ;
  • Kim, Joong-Soo (Department of Physiology, College of Dentistry, Seoul National University and Dental Research Institute) ;
  • Park, Kyung-Pyo (Department of Physiology, College of Dentistry, Seoul National University and Dental Research Institute)
  • 발행 : 2002.12.21

초록

There are some evidences that $K^+$ efflux evoked by muscarinic stimulation is not mainly mediated by large conductance $K^+$ (BK) channels in salivary gland. In this experiment, we therefore characterised non BK channels in rat submandibular gland acinar cells and examined the possibility of agonist effect on this channel using a patch clamp technique. Two types of $K^+$ channels were observed in these cells. BK channels were observed in 3 cells from total 6 cells and its average conductance was $152{\pm}7$ pS (n=3). The conductance of the another types of $K^+$ channel was estimated as $71{\pm}7$ pS (n=6). On the basis of the conductance of this channel, we defined this channel as intermediate conductance $K^+$ (IK) channels, which were observed from all 6 cells we studied. When we increased $Ca^{2+}$ concentration of the bath solution in inside-out mode, the IK channel activity was greatly increased, suggesting this channel is $Ca^{2+}$ sensitive. We next examined the effect of carbachol (CCh) and isoproterenol on the activity of the IK channels. $10^{-5}$ M isoproterenol significantly increased the open probability (Po) from $0.08{\pm}0.02$ to $0.21{\pm}0.03$ (n=4, P<0.05). Application of $10^{-5}$ M CCh also increased Po from $0.048{\pm}0.03$ to $0.55{\pm}0.33$ (n=5, P<0.05) at the maximum channel activity. The degree of BK channel activation induced by the same concentration of CCh was lower than that of IK channels; Po value was $0.011{\pm}0.003$ and $0.027{\pm}0.005$ in control and during CCh stimulation (n=3), respectively. The result suggests that IK channels exist in salivary acinar cells and its channel activity is regulated by muscaricinic and ${\beta}-adrenergic$ agonist. We conclude that IK channels also play a putative role in secretion as well as the BK channels in rat submandibular gland acinar cells.

키워드

참고문헌

  1. Christensen O, Hoffmann EK. Cell swelling activates K$^+$and Cl$^-$channels as well as nonselective, stretch-activated cation channels in Ehrlich ascites tumor cells. J Membr Biol 129(1): 13-36, 1992
  2. Cook DI, Wegman EA, Ishikawa T, Young JA. Cation channels in the parotid and mandibular glands of the sheep. In: Exocrine secretion II. P.Y.D.wong, J.A. Young. Editors. Pp.35-38. ISES. Hong Kong, 1990
  3. Devor DC, Frizzell RA. Calcium-mediated agonists activate an inwardly rectified K$^+$ channel in colonic secretory cells. Am J Physiol 265(5 Pt 1): C1271-C1280, 1993 https://doi.org/10.1152/ajpcell.1993.265.5.C1271
  4. Gallacher DV, Morris AP. A patch clamp study of potassium currents in resting and acetylcholine-stimulated mouse submandibular acinar cells. J Physiol 373: 379-395, 1986 https://doi.org/10.1113/jphysiol.1986.sp016054
  5. Hayashi T, Hirono C, Young JA, Cook DI. The Ach-induced whole cell currents in sheep parotid secretory cells. Do BK channels really carry the Ach-evoked whole cell K$^+$ current? J Membr Biol 144: 157-166, 1995
  6. Hayashi T, Young, JA, Cook DI. The ach-evoked Ca$^2+$-activated K$^+$ current in mouse mandibular secretory cells. Single channel studies. J Membr Biol 151: 19-27, 1996a https://doi.org/10.1007/s002329900054
  7. Hayashi T, Poronnik P, Young JA, Cook DI. The Ach-evoked Ca$^2+$- activated whole-cell K$^+$ current in mouse mandibular secretory cells. Whole-cell and fluorescence studies. J Membr Biol 152: 253-259, 1996b https://doi.org/10.1007/s002329900103
  8. Ishikawa T, Murakami M, Seo Y. Basolateral K$^+$ efflux is largely independent of maxi- K$^+$channels in rat submandibular glands during secretion. Pflügers Archiv 428: 516-525, 1994 https://doi.org/10.1007/BF00374573
  9. Ishikawa T, Murakami M. Tetraethylammonium-insensitive, Ca$^+$- activated whole-cell K$^+$ currents in rat submandibular acinar cells. Pflügers Arch 429: 748-750, 1995 https://doi.org/10.1007/BF00373998
  10. Jensen BS, Strobaek D, Christophersen P, Jorgensen TD, Hansen C, Silahtaroglu A, Olesen SP, Ahring PK. Characterization of the cloned human intermediate-conductance Ca$^2+$-activated K$^+$ channel. Am J Physiol 275(3 Pt 1): C848-C856, 1998 https://doi.org/10.1152/ajpcell.1998.275.3.C848
  11. Maruyama Y, Gallacher DV, Petersen OH. Volatage and Ca$^2+$- activated K$^+$ channel in basolateral acinar cell membranes in mammarian salivary glands. Nature 302, 827-829, 1987 https://doi.org/10.1038/302827a0
  12. Nauntofte B, Dissing S. K$^+$ transport and membrane potentials in isolated rat parotid acini. Am J Physiol 255: G878-G886, 1987
  13. Olesen SP, Bundgaard M. ATP-dependent closure and reactivation of inward rectifier K$^+$ channels in endothelial cells. Circ Res 73(3): 492-495, 1993 https://doi.org/10.1161/01.RES.73.3.492
  14. Park KP, Beck JS, Douglas IJ, Brown PD. Ca$^2+$-activated K$^+$ channels are involved in regulatory volume decrease in cells isolated from the rat lacrimal gland. J Membr Biol 141: 193-201, 1994
  15. Petersen OH. Stimulus-secretion coupling: cytosolic calcium signals and the control of ion channels in exocrine acinar cells. J Physiol 448: 1-51, 1992 https://doi.org/10.1113/jphysiol.1992.sp019028
  16. Sauve R, Parent L, Simoneau C, Roy G. External ATP triggers a biphasic activation process of a calcium-dependent K$^+$ channel in cultured bovine aortic endothelial cells. Pflügers Arch 412(5): 469-81, 1988 https://doi.org/10.1007/BF00582535
  17. Schmid A, Schulz I. Characterization of single potassium channels in mouse pancreatic acinar cells. J Physiol 484: 661-676, 1995 https://doi.org/10.1113/jphysiol.1995.sp020694
  18. Soltoff SP, McMillan MK, Cantley LC, Cragoe EJ, Talamo BR. Effects of muscarinic, alpha-adrenergic, and substance-P agonists and ionomycin on ion transport mechanisms in the rat parotid acinar cell. The dependence of ion transport on intracellular calcium. J Gen Physiol 95: 319-346, 1990 https://doi.org/10.1085/jgp.95.2.319
  19. Wright RD, Blair-West JR. The effects of channel blockers on ovine parotid secretion depend on the mode of stimulation. Exp Physiol 75: 339-348, 1990 https://doi.org/10.1113/expphysiol.1990.sp003408
  20. Young JA, Cook DI, Evans LA, Pirani D. Effects of ion transport inhibition on rat mandibular gland secretion. J Dent Res 66: 531-536, 1987 https://doi.org/10.1177/00220345870660022401