Agonist-like activity of antibodies directed against the second extracellular loop of the human cardiac serotonin 5-HT4(e) receptor in transfected COS-7 cells

被引:9
作者
Bozon, V
Di Scala, E
Eftekhari, P
Hoebeke, J
Lezoualc'h, F
Fischmeister, R
Argibay, J
机构
[1] Fac Sci & Tech, CNRS UMR 6542, F-37200 Tours, France
[2] Fac Med Strasbourg, Inst Pharmacol, Strasbourg, France
[3] Inst Biol Mol & Cellulaire, CNRS UPR 9021, Strasbourg, France
[4] Fac Pharm Chatenay Malabry, INSERM U 466, Lab Cardiol Cellulaire & Mol, Chatenay Malabry, France
关键词
agonist-like; anti-peptide antibody; atrial fibrillation; cAMP; COS-7; cells; 5-HT4; receptor;
D O I
10.1080/10606820212394
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
We have previously reported that antipeptide antibodies directed against the second extracellular loop of the cardiac h5-HT4 receptor could block the activation of the L-type Ca channel in human atrial cardiomyocytes. In this paper we investigate the immunological and physiological activity of these antibodies, in a cell system expressing a larger amount of receptors than the atrial cells. The recombinant receptor was expressed at the surface of COS-7 cells under an active form (serotonin, EC50 = 1.81 x 10(-7) M), at a high level (375 +/- 25 fmol receptor/mg total protein) and was able to bind a specific ligand (GR113808) with a high affinity (Kd = 0.28 +/- 0.05 nM). In this system, the same anti-peptide antibodies used for the cardiac cells induced an "agonist-like" effect on the recombinant h5-HT4 receptor. These results are in line with those shown for others G-protein coupled receptors, as adrenoreceptors. In addition, this work showed that the effect of the antibodies is not only dependent on the epitopic region recognised but also on the molecular density and/or the cellular environment of the target receptors. Finally, our results support the hypothesis that the h5-HT4 receptor could be a new target for autoantibodies in patients with atrial arrhythmia.
引用
收藏
页码:113 / 121
页数:9
相关论文
共 48 条
[1]
The N-terminal amino group of [Tyr(8)]bradykinin is bound adjacent to analogous amino acids of the human and rat B-2 receptor [J].
AbdAlla, S ;
Jarnagin, K ;
MullerEsterl, W ;
Quitterer, U .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (44) :27382-27387
[2]
ASCIMENTO JH, 2001, AM J PHYSIOL-CELL PH, V281, pC1251
[3]
5-HT4(a) and 5-HT4(b) receptors have nearly identical pharmacology and are both expressed in human atrium and ventricle [J].
Bach, T ;
Syversveen, T ;
Kvingedal, AM ;
Krobert, KA ;
Brattelid, T ;
Kaumann, AJ ;
Levy, FO .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 2001, 363 (02) :146-160
[4]
The 5-HT4 receptor antagonist ML10375 inhibits the constitutive activity of human 5-HT4(c) receptor [J].
Blondel, O ;
Gastineau, M ;
Langlois, M ;
Fischmeister, R .
BRITISH JOURNAL OF PHARMACOLOGY, 1998, 125 (04) :595-597
[5]
Molecular and functional characterization of a 5-HT4 receptor cloned from human atrium [J].
Blondel, O ;
Vandecasteele, G ;
Gastineau, M ;
Leclerc, S ;
Dahmoune, Y ;
Langlois, M ;
Fischmeister, R .
FEBS LETTERS, 1997, 412 (03) :465-474
[6]
Blondel O, 1998, J NEUROCHEM, V70, P2252
[7]
Use of a G-protein-coupled receptor to communicate. A success during evolution [J].
Bockaert, J ;
Pin, JP .
COMPTES RENDUS DE L ACADEMIE DES SCIENCES SERIE III-SCIENCES DE LA VIE-LIFE SCIENCES, 1998, 321 (07) :529-551
[8]
THE 5-HT4 RECEPTOR - A PLACE IN THE SUN [J].
BOCKAERT, J ;
FOZARD, JR ;
DUMUIS, A ;
CLARKE, DE .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1992, 13 (04) :141-145
[9]
Claeysen S, 1999, MOL PHARMACOL, V55, P910
[10]
Dzimiri N, 1999, PHARMACOL REV, V51, P465