Acidic pH-activated $Cl^-$ Current and Intracellular $Ca^{2+}$ Response in Human Keratinocytes

  • Park, Su-Jung (Departments of physiology, Seoul National University College of Medicine) ;
  • Choi, Won-Woo (Departments of Dermatology, Seoul National University College of Medicine, Laboratory of Cutaneous Aging Research, Clinical Research Institute, Seoul National University Hospital, Institute of Dermatological Science, Seoul National University) ;
  • Kwon, Oh-Sang (Departments of Dermatology, Seoul National University College of Medicine, Laboratory of Cutaneous Aging Research, Clinical Research Institute, Seoul National University Hospital, Institute of Dermatological Science, Seoul National University) ;
  • Chung, Jin-Ho (Departments of Dermatology, Seoul National University College of Medicine, Laboratory of Cutaneous Aging Research, Clinical Research Institute, Seoul National University Hospital, Institute of Dermatological Science, Seoul National University) ;
  • Eun, Hee-Chul (Departments of Dermatology, Seoul National University College of Medicine, Laboratory of Cutaneous Aging Research, Clinical Research Institute, Seoul National University Hospital, Institute of Dermatological Science, Seoul National University) ;
  • Earm, Young-E (Departments of physiology, Seoul National University College of Medicine) ;
  • Kim, Sung-Joon (Kidney Research Institute, Seoul National University)
  • Published : 2008.08.31

Abstract

The layers of keratinocytes form an acid mantle on the surface of the skin. Herein, we investigated the effects of acidic pH on the membrane current and $[Ca^{2+}]_c$ of human primary keratinocytes from foreskins and human keratinocyte cell line (HaCaT). Acidic extracellular pH ($pH_e{\leq}5.5$) activated outwardly rectifying $Cl^-$ current ($I_{Cl,pH}$) with slow kinetics of voltage-dependent activation. $I_{Cl,pH}$ was potently inhibited by an anion channel blocker 4,4'-diisothiocyanostilbene-2,2'-disulphonic acid (DIDS, 73.5% inhibition at 1${\mu}$M). $I_{Cl,pH}$ became more sensitive to $pH_e$ by raising temperature from $24^{circ}C$ to $37^{circ}C$. HaCaT cells also expressed $Ca^{2+}$-activated $Cl^-$ current ($I_{Cl,Ca}$), and the amplitude of $I_{Cl,Ca}$ was increased by relatively weak acidic $pH_e$ (7.0 and 6.8). Interestingly, the acidic $pH_e$ (5.0) also induced a sharp increase in the intracellular [$Ca^{2+}$] (${\triangle}[Ca^{2+}]_{acid}$) of HaCaT cells. The ${\triangle}[Ca^{2+}]_{acid}$ was independent of extracellular $Ca^{2+}$, and was abolished by the pretreatment with PLC inhibitor, U73122. In primary human keratinocytes, 5 out of 28 tested cells showed ${\triangle}[Ca^{2+}]_{acid}$. In summary, we found $I_{Cl,pH}$ and ${\triangle}[Ca^{2+}]_{acid}$ in human keratinocytes, and these ionic signals might have implication in pathophysiological responses and differentiation of epidermal keratinocytes.

Keywords

References

  1. Auzanneau C, Thoreau V, Kitzis A, Becq F. A novel voltage-dependent chloride current activated by extracellular acidic pH in cultured rat Sertoli cells. J Biol Chem 278: 19230-19236, 2003 https://doi.org/10.1074/jbc.M301096200
  2. Behne MJ, Meyer JW, Hanson KM, Barry NP, Murata S, Crumrine D, Clegg RW, Gratton E, Holleran WM, Elias PM, Mauro TM. NEH1 regulates the stratum corneum permeability barrier homeostasis. J Biol Chem 277: 47299-47406, 2002
  3. Boyce ST, Ham RG. Calcium-regulated differentiation of normal human epidermal keratinocytes in chemically defined clonal culture and serum-free serial culture. J Invest Dermatol 81(1 Suppl): 33s-40s, 1983 https://doi.org/10.1111/1523-1747.ep12540422
  4. Elias PM, Ahn SK, Brown BE, Crumrine D, Feingold KR. Origin of the epidermal calcium gradient: regulation by barrier status and role of active vs passive mechanisms. J Invest Dermatol 119: 1269-1274, 2002 https://doi.org/10.1046/j.1523-1747.2002.19622.x
  5. Fluhr JW, Kao J, Jain M, Ahn SK, Feingold KR, Elias PM. Generation of free fatty acids from phospholipids regulates stratum corneum acidification and integrity. J Invest Dermatol 117: 44-51, 2001 https://doi.org/10.1046/j.0022-202x.2001.01399.x
  6. Fluhr JW, Mao-Qiang M, Brown BE, Hachem J-P, Moskowitz DG, Demerjian M, Haftek M, Serre G, Crumrine D, Mauro TM, Elias PM, Feingold KR. Functional consequences of a neutral pH in neonatal rat stratum corneum. J Invest Dermatol 123: 140-151, 2004 https://doi.org/10.1111/j.0022-202X.2004.22726.x
  7. Frosch P, Kligman AM. Method for appraising the sting capacity of topically applied substances. J Soc Cosmetic Chem 28: 197-209, 1977
  8. Hachem J-P, Crumrine D, Fluhr J, Brown BE, Feingold KR, Elias PM. pH directly regulates epidermal permeability barrier homeostasis, and stratum corneum integrity/cohesion. J Invest Dermatol 121: 345-353, 2003 https://doi.org/10.1046/j.1523-1747.2003.12365.x
  9. Hirayama Y, Kuruma A, Hiraoka M, Kawano S. Calcium-activated $Cl_-$ current is enhanced by acidosis and contributes to the shortening of action potential duration in rabbit ventricular myocytes. Jpn J Physiol 52: 293-300, 2002 https://doi.org/10.2170/jjphysiol.52.293
  10. Ishii S, Kihara Y, Shimizu T. Identification of T cell death- associated gene 8 (TDAG8) as a novel acid sensing G-protein- coupled receptor. J Biol Chem 280: 9083-9087, 2005 https://doi.org/10.1074/jbc.M407832200
  11. Koegel H, Alzheimer C. Expression and biological significance of $Ca^2+$-activated ion channels in human keratinocytes. FASEB J 15: 145-154, 2001 https://doi.org/10.1096/fj.00-0055com
  12. Lambert S, Oberwinkler J. Characterization of a proton-activated, outwardly rectifying anion channel. J Physiol 567: 191-213, 2005
  13. Lang F, Foller M, Lang KS, Lang PA, Ritter M, Gulbins E, Vereninov A, Huber SM. Ion channels in cell proliferation and apoptotic cell death. J Memb Biol 205: 147-157, 2005 https://doi.org/10.1007/s00232-005-0780-5
  14. Lehen'kyi V, Beck B, Polakowska R, Charveron M, Bordat P, Skryma R, Prevarskaya N. TRPV6 is a $Ca^2+$ entry channel essential for $Ca^2+$-induced differentiation of human keratinocytes. J Biol Chem 282: 22582-22591, 2007 https://doi.org/10.1074/jbc.M611398200
  15. Ludwig M-G, Vanek M, Guerini D, Gasser JA, Jones CE, Junker W, Hofstetter H, Wolf RM, Seuwen K. Proton-sensing G-protein coupled receptors. Nature 425: 93-98, 2003 https://doi.org/10.1038/nature01905
  16. Menkin V. Chemical mediators in relation to cytologic constituents in inflammation. Am J Pathol 34: 921-941, 1958
  17. Menon GK, Elias PM, Lee SH, Feingold KR. Localization of calcium in murine epidermis following disruption and repair of the permeability barrier. Cell Tissue Res 270: 503-512, 1992 https://doi.org/10.1007/BF00645052
  18. Murakami N, Yokomizo T, Okuno T, Shimizu T. G2A is a proton- sensing G-protein-coupled receptor antagonized by lysophosphatidylcholine. J Biol Chem 279: 42484-42491, 2004 https://doi.org/10.1074/jbc.M406561200
  19. Nilius B, Droogmans G. Amazing chloride channels: an overview. Acta Physiol Scand 177: 119-147, 2003 https://doi.org/10.1046/j.1365-201X.2003.01060.x
  20. Nobles M, Higgins CF, Sardini A. Extracellular acidification elicits a chloride current that shares characteristics with $I_Cl(swell)$. Am J Physiol Cell Physiol 287: C1426-C1435, 2004 https://doi.org/10.1152/ajpcell.00549.2002
  21. Okada Y, Maeno E, Shimizu T, Manabe K, Mori S, Nabekura T. Dual roles of plasmalemmal chloride channels in induction of cell death. Pflugers Arch 448: 287-295, 2004 https://doi.org/10.1007/s00424-004-1276-3
  22. Silver RB. Ratio imaging: practical considerations for measuring intracellular calcium and pH in living tissue. Methods Cell Biol 56: 237-251, 1998 https://doi.org/10.1016/S0091-679X(08)60429-X
  23. Smith JB, Dwyer SD, Smith L. Lowering extracellular pH evokes inositol polyphosphate formation and calcium mobilization. J Biol Chem 264: 8723-8728, 1989
  24. Tu C-L, Chang W, Bikle DD. The extracellular calcium-sensing receptor is required for calcium-induced differentiation in human keratinocytes. J Biol Chem 276: 41079-41085, 2001 https://doi.org/10.1074/jbc.M107122200
  25. Wang H-Y, Shimizu T, Numata T, Okada Y. Role of acid-sensitive outwardly rectifying anion channels in acidosis-induced cell death in human epithelial cells. Pflugers Arch 454: 223-233, 2007 https://doi.org/10.1007/s00424-006-0193-z
  26. Willis CM, Shaw S, Lacharriere ODE, Baverel M, Reiche L, Jourdain R, Bastien P, Wilkinson J. Sensitive skin: an epidemiological study. Br J Dermatol 145: 258-263, 2001 https://doi.org/10.1046/j.1365-2133.2001.04343.x
  27. Yamamoto S, Ehara T. Acidic extracellular pH-activated outwardly rectifying chloride current in mammalian cardiac myocytes. Am J Physiol Heart Circ Physiol 290: H1905-H1914, 2006 https://doi.org/10.1152/ajpheart.00965.2005
  28. Yuspa SH, Kilkenny AE, Steinert PM, Roop DR. Expression of murine epidermal differentiation markers is tightly regulated by restricted extracellular calcium concentrations in vitro. J Cell Biol 109: 1207-1217, 1989 https://doi.org/10.1083/jcb.109.3.1207