Characterization of multiple P2X receptors in cultured normal human epidermal keratinocytes

被引:49
作者
Inoue, K
Denda, M
Tozaki, H
Fujishita, K
Koizumi, S
Inoue, K
机构
[1] Shiseido Res Ctr, Kanazawa Ku, Yokohama, Kanagawa 2368643, Japan
[2] Natl Inst Hlth Sci, Div Biosignaling, Tokyo 158, Japan
[3] Kyushu Univ, Grad Sch Pharmaceut Sci, Fukuoka 812, Japan
[4] Natl Inst Hlth Sci, Div Pharmacol, Tokyo 158, Japan
关键词
ATP; channel; differentiation; intracellular calcium;
D O I
10.1111/j.0022-202X.2005.23683.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
ATP-gated ion channels (P2X) are expressed in human epidermis and cultured keratinocytes. The aim of this study was to characterize native P2X receptors in normal human epidermal keratinocytes (NHEK) using whole-cell patch clamp technique, RT-PCR, and determination of intracellular Ca2+ concentration ([Ca2+](i)). Application of ATP resulted in an inward current with a reversal potential of 0 mV. Response to ATP showed two types of currents: the slowly desensitizing response and the rapidly desensitizing response. The slowly desensitizing response was blocked by iso-pyridocaphosphate-6-azophenyl-2', 5' disulfonic acid (PPADS), a P2X receptor antagonist. We found that the expression of multiple P2X(2), P2X(3), P2X(5), and P2X(7) receptor subtype mRNA was increased in differentiated cells. On the other hand, the expression of G-protein-coupled P2Y(2) mRNA was downregulated in differentiated cells. Increases in [Ca2+](i) evoked by alpha beta-methylene ATP (alpha beta-meATP) and 2', 3'-O-(4-benzoylbenzoyl) ATP (BzATP) were elevated, whereas elevation of [Ca2+](i) evoked by uridine 5'-triphosphate (UTP) was decreased in differentiated cells. Application of ATP or UVB radiation increased the expression of P2X(1), P2X(2), P2X(3), and P2X(7) receptors in NHEK. Changes in the expression levels and cation influx via multiple P2X receptors might be involved in the regulation of differentiation and one of the epidermal external sensors.
引用
收藏
页码:756 / 763
页数:8
相关论文
共 35 条
[1]   Pharmacological and biophysical properties of the human P2X5 receptor [J].
Bo, XN ;
Jiang, LH ;
Wilson, HL ;
Kim, M ;
Burnstock, G ;
Surprenant, A ;
North, RA .
MOLECULAR PHARMACOLOGY, 2003, 63 (06) :1407-1416
[2]   Purinergic receptors: Their role in nociception and primary afferent neurotransmission [J].
Burnstock, G ;
Wood, JN .
CURRENT OPINION IN NEUROBIOLOGY, 1996, 6 (04) :526-532
[3]   Human keratinocytes express multiple P2Y-receptors:: Evidence for functional P2Y1, P2Y2, and P2Y4 receptors [J].
Burrell, HE ;
Bowler, WB ;
Gallagher, JA ;
Sharpe, GR .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2003, 120 (03) :440-447
[4]   A P2X PURINOCEPTOR EXPRESSED BY A SUBSET OF SENSORY NEURONS [J].
CHEN, CC ;
AKOPIAN, AN ;
SIVILOTTI, L ;
COLQUHOUN, D ;
BURNSTOCK, G ;
WOOD, JN .
NATURE, 1995, 377 (6548) :428-431
[5]   Cell damage excites nociceptors through release of cytosolic ATP [J].
Cook, SP ;
McCleskey, EW .
PAIN, 2002, 95 (1-2) :41-47
[6]   P2X purinergic receptor antagonist accelerates skin barrier repair and prevents epidermal hyperplasia induced by skin barrier disruption [J].
Denda, M ;
Inoue, K ;
Fuziwara, S ;
Denda, S .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2002, 119 (05) :1034-1040
[7]   Regulation of epidermal homeostasis through P2Y2 receptors [J].
Dixon, CJ ;
Bowler, WB ;
Littlewood-Evans, A ;
Dillon, JP ;
Bilbe, G ;
Sharpe, GR ;
Gallagher, JA .
BRITISH JOURNAL OF PHARMACOLOGY, 1999, 127 (07) :1680-1686
[8]   P2X receptors in autonomic and sensory neurons [J].
Evans, RJ ;
Surprenant, A .
SEMINARS IN THE NEUROSCIENCES, 1996, 8 (04) :217-223
[9]   ATP is released from rabbit urinary bladder epithelial cells by hydrostatic pressure changes - a possible sensory mechanism? [J].
Ferguson, DR ;
Kennedy, I ;
Burton, TJ .
JOURNAL OF PHYSIOLOGY-LONDON, 1997, 505 (02) :503-511
[10]   ATP-mediated cytotoxicity in microglial cells [J].
Ferrari, D ;
Chiozzi, P ;
Falzoni, S ;
DalSusino, M ;
Collo, G ;
Buell, G ;
DiVirgilio, F .
NEUROPHARMACOLOGY, 1997, 36 (09) :1295-1301