Distinct functions of the two isoforms of dopamine D2 receptors

被引:543
作者
Usiello, A
Baik, JH
Rougé-Pont, F
Picetti, R
Dierich, A
LeMeur, M
Piazza, PV
Borrelli, E
机构
[1] ULP, INSERM, CNRS, Inst Genet & Biol Mol & Cellulaire, F-67404 Illkirch Graffenstaden, CU Strasbourg, France
[2] Univ Bordeaux 2, INSERM, U259, F-33077 Bordeaux, France
关键词
D O I
10.1038/35041572
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Signalling through dopamine D2 receptors governs physiological functions related to locomotion, hormone production and drug abuse(1-7). D2 receptors are also known targets of antipsychotic drugs that are used to treat neuropsychiatric disorders such as schizophrenia(8). By a mechanism of alternative splicing, the D2 receptor gene encodes two molecularly distinct isoforms(9), D2S and D2L, previously thought to have the same function. Here we show that these receptors have distinct functions in vivo; D2L acts mainly at postsynaptic sites and D2S serves presynaptic autoreceptor functions. The cataleptic effects of the widely used antipsychotic haloperidol(1) are absent in D2L-deficient mice. This suggests that D2L is targeted by haloperidol, with implications for treatment of neuropsychiatric disorders. The absence of D2L reveals that D2S inhibits D1 receptor-mediated functions, uncovering a circuit of signalling interference between dopamine receptors.
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页码:199 / 203
页数:6
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