Cystic fibrosis transmembrane conductance regulator (CFTR) confers glibenclamide sensitivity to outwardly rectifying chloride channel (ORCC) in Hi-5 insect cells

被引:18
作者
Julien, M
Verrier, B
Cerutti, M
Chappe, V
Gola, M
Devauchelle, G
Becq, F [1 ]
机构
[1] INRA CNRS, Stn Rech Pathol Comparee, F-30380 St Christol Lez Ales, France
[2] CNRS, UPR 9024, Neurobiol Lab, F-13402 Marseille 20, France
关键词
Trichoplusia ni insect cells (Hi-5); baculovirus; cystic fibrosis transmembrane conductance; regulator (CFTR) chloride channel; glibenclamide; outwardly rectifying chloride channel (ORCC);
D O I
10.1007/s002329900512
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Increasing evidence is now accumulating for the involvement of the cystic fibrosis transmembrane conductance regulator (CFTR) in the control of the outwardly rectifying chloride channel (ORCC). We have examined the sensitivity of ORCC to the sulfonylurea drug glibenclamide in Hi-5 (Trichoplusia ni) insect cells infected with recombinant baculovirus expressing either wild-type CFTR, Delta F508-CFTR or E. coli beta galactosidase cDNA and in control cells either infected with virus alone or uninfected. Iodide efflux and single channel patch-clamp experiments confirmed that forskolin and 1-methyl-3-isobutyl xanthine (IBMX) or 7-methyl-1,3 dipropyl xanthine (DPMX) activate CFTR channels (unitary conductance: 9.1 +/- 1.6 pS) only in cells expressing CFTR. In contrast, we identified 4-acetamido-4'-isothiocyanatostilbene-2,2'-disulfonic acid (SITS)-sensitive ORCC in excised membrane patches in any of the cells studied, with similar conductance (22 +/- 2.5 pS at -80 mV; 55 +/- 4.1 pS at +80 mV) and properties. In the presence of 500 mu M SITS, channel open probability (P-o) of ORCC was reversibly reduced to 0.05 +/- 0.01 in CFTR-cells, to 0.07 +/- 0.02 in non-CFTR expressing cells and to 0.05 +/- 0.02 in Delta F508-cells. In Hi-5 cells that did not express CFTR, glibenclamide failed to inhibit ORCC activity even at high concentrations (100 mu M), whereas 500 mu M SITS reversibly inhibited ORCC. In contrast in cells expressing CFTR or Delta F508, glibenclamide dose dependently (IC50 = 17 mu M, Hill coefficient 1.2) and reversibly inhibited ORCC. Cytoplasmic application of 100 mu M glibenclamide reversibly reduced P-o from 0.88 +/- 0.03 to 0.09 +/- 0.02 (wash: P-o = 0.85 +/- 0.1) in CFTR cells and from 0.89 +/- 0.05 to 0.08 +/- 0.05 (wash: P-o = 0.87 +/- 0.1) in Delta F508 cells. In non-CFTR expressing cells, glibenclamide (100 mu M) was without effect on P-o (control: P-o = 0.89 +/- 0.09, glib.: P-o = 0.86 +/- 0.02; wash: P-o = 0.87 +/- 0.05). These data strongly suggest that the expression of CFTR confers glibenclamide sensitivity to the ORCC in Hi-5 cells.
引用
收藏
页码:229 / 239
页数:11
相关论文
共 51 条
[1]   THE SULFONYLUREA RECEPTOR [J].
ASHCROFT, SJH ;
ASHCROFT, FM .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1175 (01) :45-49
[2]   DEFECTIVE ACIDIFICATION OF INTRACELLULAR ORGANELLES IN CYSTIC-FIBROSIS [J].
BARASCH, J ;
KISS, B ;
PRINCE, A ;
SAIMAN, L ;
GRUENERT, D ;
ALAWQATI, Q .
NATURE, 1991, 352 (6330) :70-73
[3]   ANION CHANNELS IN A HUMAN PANCREATIC-CANCER CELL-LINE (CAPAN-1) OF DUCTAL ORIGIN [J].
BECQ, F ;
FANJUL, M ;
MAHIEU, I ;
BERGER, Z ;
GOLA, M ;
HOLLANDE, E .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1992, 420 (01) :46-53
[4]   ABC1, an ATP binding cassette transporter required for phagocytosis of apoptotic cells, generates a regulated anion flux after expression in Xenopus laevis oocytes [J].
Becq, F ;
Hamon, Y ;
Bajetto, A ;
Gola, M ;
Verrier, B ;
Chimini, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (05) :2695-2699
[5]   cAMP- and Ca2+-independent activation of cystic fibrosis transmembrane conductance regulator channels by phenylimidazothiazole drugs [J].
Becq, F ;
Verrier, B ;
Chang, XB ;
Riordan, JR ;
Hanrahan, JW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (27) :16171-16179
[6]   PHOSPHORYLATION-REGULATED LOW-CONDUCTANCE CL-CHANNELS IN A HUMAN PANCREATIC DUCT CELL-LINE [J].
BECQ, F ;
HOLLANDE, E ;
GOLA, M .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1993, 425 (1-2) :1-8
[7]   Structural basis for specificity and potency of xanthine derivatives as activators of the CFTR chloride channel [J].
Chappe, V ;
Mettey, Y ;
Vierfond, JM ;
Hanrahan, JW ;
Gola, M ;
Verrier, B ;
Becq, F .
BRITISH JOURNAL OF PHARMACOLOGY, 1998, 123 (04) :683-693
[8]   DEFECTIVE INTRACELLULAR-TRANSPORT AND PROCESSING OF CFTR IS THE MOLECULAR-BASIS OF MOST CYSTIC-FIBROSIS [J].
CHENG, SH ;
GREGORY, RJ ;
MARSHALL, J ;
PAUL, S ;
SOUZA, DW ;
WHITE, GA ;
ORIORDAN, CR ;
SMITH, AE .
CELL, 1990, 63 (04) :827-834
[9]   ALTERED CHLORIDE-ION CHANNEL KINETICS ASSOCIATED WITH THE DELTA-F508 CYSTIC-FIBROSIS MUTATION [J].
DALEMANS, W ;
BARBRY, P ;
CHAMPIGNY, G ;
JALLAT, S ;
DOTT, K ;
DREYER, D ;
CRYSTAL, RG ;
PAVIRANI, A ;
LECOCQ, JP ;
LAZDUNSKI, M .
NATURE, 1991, 354 (6354) :526-528
[10]   PROCESSING OF MUTANT CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR IS TEMPERATURE-SENSITIVE [J].
DENNING, GM ;
ANDERSON, MP ;
AMARA, JF ;
MARSHALL, J ;
SMITH, AE ;
WELSH, MJ .
NATURE, 1992, 358 (6389) :761-764