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Myometrial relaxation of mice via expression of two pore domain acid sensitive K+ (TASK-2) channels

  • Kyeong, Kyu-Sang (Department of Obstetrics and Gynecology, Chungbuk National University College of Medicine) ;
  • Hong, Seung Hwa (Department of Obstetrics and Gynecology, Chungbuk National University College of Medicine) ;
  • Kim, Young Chul (Department of Physiology, Chungbuk National University College of Medicine) ;
  • Choi, Woong (Department of Pharmacology, Chungbuk National University College of Medicine) ;
  • Myung, Sun Chul (Department of Urology, College of Medicine, Chung-Ang University) ;
  • Lee, Moo Yeol (Department of Physiology, College of Medicine, Chung-Ang University) ;
  • You, Ra Young (Department of Physiology, Chungbuk National University College of Medicine) ;
  • Kim, Chan Hyung (Department of Pharmacology, Chungbuk National University College of Medicine) ;
  • Kwon, So Yeon (VHS Medical Center) ;
  • Suzuki, Hikaru (Department of Physiology, Nagoya City University Medical School) ;
  • Park, Yeon Jin (Department of Obstetrics and Gynecology, Cheongju St. Mary's Hospital) ;
  • Jeong, Eun-Hwan (Department of Obstetrics and Gynecology, Chungbuk National University College of Medicine) ;
  • Kim, Hak Soon (Department of Obstetrics and Gynecology, Chungbuk National University College of Medicine) ;
  • Kim, Heon (Department of Preventive Medicine, Chungbuk National University College of Medicine) ;
  • Lim, Seung Woon (Department of Anesthesiology and Pain Medicine, Chungbuk National University College of Medicine) ;
  • Xu, Wen-Xie (Department of Physiology, Shanghai Jiaotong University, School of Medicine) ;
  • Lee, Sang Jin (Department of Medical Education, Chungbuk National University College of Medicine) ;
  • Ji, Il Woon (Department of Obstetrics and Gynecology, Chungbuk National University College of Medicine)
  • Received : 2016.07.04
  • Accepted : 2016.08.08
  • Published : 2016.09.01

Abstract

Myometrial relaxation of mouse via expression of two-pore domain acid sensitive (TASK) channels was studied. In our previous report, we suggested that two-pore domain acid-sensing $K^+$ channels (TASK-2) might be one of the candidates for the regulation of uterine circular smooth muscles in mice. In this study, we tried to show the mechanisms of relaxation via TASK-2 channels in marine myometrium. Isometric contraction measurements and patch clamp technique were used to verify TASK conductance in murine myometrium. Western blot and immunehistochemical study under confocal microscopy were used to investigate molecular identity of TASK channel. In this study, we showed that TEA and 4-AP insensitive non-inactivating outward $K^+$ current (NIOK) may be responsible for the quiescence of murine pregnant longitudinal myometrium. The characteristics of NIOK coincided with two-pore domain acid-sensing $K^+$ channels (TASK-2). NIOK in the presence of $K^+$ channel blockers was inhibited further by TASK inhibitors such as quinidine, bupivacaine, lidocaine, and extracellular acidosis. Furthermore, oxytocin and estrogen inhibited NIOK in pregnant myometrium. When compared to non-pregnant myometrium, pregnant myometrium showed stronger inhibition of NIOK by quinidine and increased immunohistochemical expression of TASK-2. Finally, TASK-2 inhibitors induced strong myometrial contraction even in the presence of L-methionine, a known inhibitor of stretch-activated channels in the longitudinal myometrium of mouse. Activation of TASK-2 channels seems to play an essential role for relaxing uterus during pregnancy and it might be one of the alternatives for preventing preterm delivery.

Keywords

References

  1. Parkington HC, Coleman HA. Excitability in uterine smooth muscle. Front Horm Res. 2001;27:179-200.
  2. Sanborn BM. Ion channels and the control of myometrial electrical activity. Semin Perinatol. 1995;19:31-40 https://doi.org/10.1016/S0146-0005(95)80045-X
  3. Garfield RE, Sims S, Daniel EE. Gap junctions: their presence and necessity in myometrium during parturition. Science. 1977;198:958-960. https://doi.org/10.1126/science.929182
  4. Wray S, Noble K. Sex hormones and excitation-contraction coupling in the uterus: the effects of oestrous and hormones. J Neuroendocrinol. 2008;20:451-461. https://doi.org/10.1111/j.1365-2826.2008.01665.x
  5. Cerri V, Tarantini M, Zuliani G, Schena V, Redaelli C, Nicolini U. Intravenous glucose infusion in labor does not affect maternal and fetal acid-base balance. J Matern Fetal Med. 2000;9:204-208.
  6. Sjostedt S. Acid-base balance of arterial blood during pregnancy, at delivery, and in the puerperium. Am J Obstet Gynecol. 1962;84:775-779. https://doi.org/10.1016/0002-9378(62)90032-7
  7. Harrison N, Larcombe-McDouall JB, Earley L, Wray S.An in vivo study of the effects of ischaemia on uterine contraction, intracellular pH and metabolites in the rat. J Physiol. 1994;476:349-354. https://doi.org/10.1113/jphysiol.1994.sp020136
  8. Brinkman CR. Circulation in the pregnant uterus. In: Carsten ME, Miller JD, editors. Uterine function: molecular and cellular aspects. New York: Plenum Press; 1990. p.519-537.
  9. Csapo A. Progesterone block. Am J Anat. 1956;98:273-291. https://doi.org/10.1002/aja.1000980206
  10. Tulchinsky D, Hobel CJ, Yeager E, Marshall JR. Plasma estrone, estradiol, estriol, progesterone, and 17-hydroxyprogesterone in human pregnancy. I. Normal pregnancy. Am J Obstet Gynecol. 1972;112:1095-1100. https://doi.org/10.1016/0002-9378(72)90185-8
  11. Walsh SW, Stanczyk FZ, Novy MJ. Daily hormonal changes in the maternal, fetal, and amniotic fluid compartments before parturition in a primate species. J Clin Endocrinol Metab. 1984;58:629-639. https://doi.org/10.1210/jcem-58-4-629
  12. Hong SH, Kyeong KS, Kim CH, Kim YC, Choi W, Yoo RY, Kim HS, Park YJ, Ji IW, Jeong EH, Kim HS, Xu WX, Lee SJ. Regulation of myometrial contraction by ATP-sensitive potassium (KATP) channel via activation of SUR2B and Kir 6.2 in mouse. J Vet Med Sci. 2016;78:1153-1159. https://doi.org/10.1292/jvms.15-0700
  13. Park JK, Kim YC, Sim JH, Choi MY, Choi W, Hwang KK, Cho MC, Kim KW, Lim SW, Lee SJ. Regulation of membrane excitability by intracellular pH (pHi) changers through $Ca^{2+}$-activated $K^{+}$ current (BK channel) in single smooth muscle cells from rabbit basilar artery. Pflugers Arch. 2007;454:307-319. https://doi.org/10.1007/s00424-007-0204-8
  14. Smith RC, McClure MC, Smith MA, Abel PW, Bradley ME. The role of voltage-gated potassium channels in the regulation of mouse uterine contractility. Reprod Biol Endocrinol. 2007;5:41-52. https://doi.org/10.1186/1477-7827-5-41
  15. Wray S, Burdyga T, Noble D, Noble K, Borysova L, Arrowsmith S. Progress in understanding electro-mechanical signalling in the myometrium. Acta Physiol (Oxf). 2015;213:417-431. https://doi.org/10.1111/apha.12431
  16. Anwer K, Oberti C, Perez GJ, Perez-Reyes N, McDougall JK, Monga M, Sanborn BM, Stefani E, Toro L. Calcium-activated $K^{+}$ channels as modulators of human myometrial contractile activity. Am J Physiol. 1993;265:C976-985. https://doi.org/10.1152/ajpcell.1993.265.4.C976
  17. Brayden JE, Nelson MT. Regulation of arterial tone by activation of calcium-dependent potassium channels. Science. 1992;256:532-535. https://doi.org/10.1126/science.1373909
  18. Bai X, Bugg GJ, Greenwood SL, Glazier JD, Sibley CP, Baker PN, Taggart MJ, Fyfe GK. Expression of TASK and TREK, two-pore domain $K^{+}$ channels, in human myometrium. Reproduction. 2005;129:525-530. https://doi.org/10.1530/rep.1.00442
  19. Ketchum KA, Joiner WJ, Sellers AJ, Kaczmarek LK, Goldstein SA. A new family of outwardly rectifying potassium channel proteins with two pore domains in tandem. Nature. 1995;376:690-695. https://doi.org/10.1038/376690a0
  20. O'Connell AD, Morton MJ, Hunter M. Two-pore domain $K^{+}$ channels-molecular sensors. Biochim Biophys Acta. 2002;1566:152-161. https://doi.org/10.1016/S0005-2736(02)00597-7
  21. Hong SH, Sung R, Kim YC, Suzuki H, Choi W, Park YJ, Ji IW, Kim CH, Myung SC, Lee MY, Kang TM, You RY, Lee KJ, Lim SW, Yun HY, Song YJ, Xu WX, Kim HS, Lee SJ. Mechanism of relaxation via TASK-2 channels in uterine circular muscle of mouse. Korean J Physiol Pharmacol. 2013;17:359-365. https://doi.org/10.4196/kjpp.2013.17.4.359
  22. Duprat F, Lesage F, Fink M, Reyes R, Heurteaux C, Lazdunski M. TASK, a human background $K^{+}$ channel to sense external pH variations near physiological pH. EMBO J. 1997;16:5464-5471. https://doi.org/10.1093/emboj/16.17.5464
  23. Kim YC, Suzuki H, Xu WX, Hashitani H, Choi W, Yun HY, Park SM, Youn SJ, Lee SJ, Lee SJ. Voltage-dependent $Ca^{2+}$ current identified in freshly isolated interstitial clls of cajal (ICC) of Guineapig stomach. Korean J Physiol Pharmacol. 2008;12:323-330. https://doi.org/10.4196/kjpp.2008.12.6.323
  24. Reyes R, Duprat F, Lesage F, Fink M, Salinas M, Farman N, Lazdunski M. Cloning and expression of a novel pH-sensitive two pore domain $K^{+}$ channel from human kidney. J Biol Chem. 1998;273:30863-30869. https://doi.org/10.1074/jbc.273.47.30863
  25. Buxton IL, Singer CA, Tichenor JN. Expression of stretch-activated two-pore potassium channels in human myometrium in pregnancy and labor. PLoS One. 2010;5:e12372. https://doi.org/10.1371/journal.pone.0012372
  26. Monaghan K, Baker SA, Dwyer L, Hatton WC, Sik Park K, Sanders KM, Koh SD. The stretch-dependent potassium channel TREK-1 and its function in murine myometrium. J Physiol. 2011;589:1221-1233. https://doi.org/10.1113/jphysiol.2010.203869
  27. Miller P, Kemp PJ, Lewis A, Chapman CG, Meadows HJ, Peers C. Acute hypoxia occludes hTREK-1 modulation: re-evaluation of the potential role of tandem P domain $K^{+}$ channels in central neuroprotection. J Physiol. 2003;548:31-37.
  28. Kang D, Mariash E, Kim D. Functional expression of TRESK-2, a new member of the tandem-pore $K^{+}$ channel family. J Biol Chem. 2004;279:28063-28070. https://doi.org/10.1074/jbc.M402940200
  29. Che T, Sun H, Li J, Yu X, Zhu D, Xue B, Liu K, Zhang M, Kunze W, Liu C. Oxytocin hyperpolarizes cultured duodenum myenteric intrinsic primary afferent neurons by opening BK(Ca) channels through $IP_3$ pathway. J Neurochem. 2012;121:516-525. https://doi.org/10.1111/j.1471-4159.2012.07702.x
  30. Soriano S, Ripoll C, Fuentes E, Gonzalez A, Alonso-Magdalena P, Ropero AB, Quesada I, Nadal A. Regulation of K(ATP) channel by 17${\beta}$-estradiol in pancreatic ${\beta}$-cells. Steroids. 2011;76:856-860.
  31. Druzin M, Malinina E, Grimsholm O, Johansson S. Mechanism of estradiol-induced block of voltage-gated $K^{+}$ currents in rat medial preoptic neurons. PLoS One. 2011;6:e20213. https://doi.org/10.1371/journal.pone.0020213
  32. Ma XY, Yu JM, Zhang SZ, Liu XY, Wu BH, Wei XL, Yan JQ, Sun HL, Yan HT, Zheng JQ. External $Ba^{2+}$ block of the two-pore domain potassium channel TREK-1 defines conformational transition in its selectivity filter. J Biol Chem. 2011;286:39813-39822. https://doi.org/10.1074/jbc.M111.264788
  33. Naderali EK, Wray S. Modulation of force induced by pH in the guinea-pig uterus examined at two stages of the oestrous cycle. J Reprod Fertil. 1999;117:153-157. https://doi.org/10.1530/jrf.0.1170153
  34. Taggart MJ, Sheader EA, Walker SD, Naderali EK, Moore S, Wray S. External alkalinization decreases intracellular Ca++ and spontaneous contractions in pregnant rat myometrium. Am J Obstet Gynecol. 1997;177:959-963. https://doi.org/10.1016/S0002-9378(97)70301-6
  35. Rooth G, Sjostedt S. The placental transfer of gases and fixed acids. Arch Dis Child. 1962;37:366-370. https://doi.org/10.1136/adc.37.194.366
  36. Parratt JR, Taggart MJ, Wray S. Functional effects of intracellular pH alteration in the human uterus: simultaneous measurements of pH and force. J Reprod Fertil. 1995;105:71-75. https://doi.org/10.1530/jrf.0.1050071
  37. Taggart M, Wray S. Simultaneous measurement of intracellular pH and contraction in uterine smooth muscle. Pflugers Arch. 1993;423:527-529. https://doi.org/10.1007/BF00374951
  38. Soloff MS, Fernstrom MA, Periyasamy S, Soloff S, Baldwin S, Wieder M. Regulation of oxytocin receptor concentration in rat uterine explants by estrogen and progesterone. Can J Biochem Cell Biol. 1983;61:625-630. https://doi.org/10.1139/o83-078
  39. Mesiano S, Welsh TN. Steroid hormone control of myometrial contractility and parturition. Semin Cell Dev Biol. 2007;18:321-331 https://doi.org/10.1016/j.semcdb.2007.05.003
  40. Khan RN, Matharoo-Ball B, Arulkumaran S, Ashford ML. Potassium channels in the human myometrium. Exp Physiol. 2001;86:255-264. https://doi.org/10.1113/eph8602181
  41. Khan RN, Smith SK, Morrison JJ, Ashford ML. $Ca^{2+}$ dependence and pharmacology of large-conductance $K^{+}$ channels in nonlabor and labor human uterine myocytes. Am J Physiol. 1997;273:C1721-1731. https://doi.org/10.1152/ajpcell.1997.273.5.C1721
  42. Wray S. Insights into the uterus. Exp Physiol. 2007;92:621-631. https://doi.org/10.1113/expphysiol.2007.038125

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