Dopamine D2 and D3 receptors are linked to the actin cytoskeleton via interaction with filamin A

被引:159
作者
Lin, RW [1 ]
Karpa, K
Kabbani, N
Goldman-Rakic, P
Levenson, R
机构
[1] Yale Univ, Sch Med, Neurobiol Sect, New Haven, CT 06510 USA
[2] Penn State Univ, Coll Med, Dept Pharmacol, Hershey, PA 17033 USA
[3] Penn State Univ, Coll Med, Grad Program Neurosci, Hershey, PA 17033 USA
关键词
D O I
10.1073/pnas.011538198
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
We have used a yeast two-hybrid approach to uncover protein interactions involving the D2-like subfamily of dopamine receptors. Using the third intracellular loop of the D2S and D3 dopamine receptors as bait to screen a human brain cDNA library, we identified filamin A (FLN-A) as a protein that interacts with both the D2 and D3 subtypes, The interaction with FLN-A was specific for the D2 and D3 receptors and was independently confirmed in pull-down and coimmunoprecipitation experiments. Deletion mapping localized the dopamine receptor-FLN-A interaction to the N-terminal segment of the D2 and D3 dopamine receptors and to repeat 19 of FLN-A, In cultures of dissociated rat striatum, FLN-A and D2 receptors colocalized throughout neuronal somata and processes as well as in astrocytes. Expression of D2 dopamine receptors in FLN-A-deficient M2 melanoma cells resulted in predominant intracellular localization of the D2 receptors, whereas in FLN-A-reconstituted cells, the D2 receptor was predominantly localized at the plasma membrane. These results suggest that FLN-A may be required for proper cell surface expression of the D2 dopamine receptors, Association of D2 and D3 dopamine receptors with FLN-A provides a mechanism whereby specific dopamine receptor subtypes may be functionally linked to downstream signaling components via the actin cytoskeleton.
引用
收藏
页码:5258 / 5263
页数:6
相关论文
共 37 条
[1]  
Bellanger Jean-Michel, 1998, Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales, V192, P367
[2]   HALOPERIDOL-INDUCED PLASTICITY OF AXON TERMINALS IN RAT SUBSTANTIA NIGRA [J].
BENES, FM ;
PASKEVICH, PA ;
DOMESICK, VB .
SCIENCE, 1983, 221 (4614) :969-971
[3]   SYNAPTIC REARRANGEMENTS IN MEDIAL PREFRONTAL CORTEX OF HALOPERIDOL-TREATED RATS [J].
BENES, FM ;
PASKEVICH, PA ;
DAVIDSON, J ;
DOMESICK, VB .
BRAIN RESEARCH, 1985, 348 (01) :15-20
[4]  
CARRAWAY KL, 1998, SIGNALING CYTOSKELET
[5]  
CIVELLI O, 1993, ANN REV PHARM TOXICO, V32, P281
[6]   THE RETINOBLASTOMA PROTEIN ASSOCIATES WITH THE PROTEIN PHOSPHATASE TYPE-1 CATALYTIC SUBUNIT [J].
DURFEE, T ;
BECHERER, K ;
CHEN, PL ;
YEH, SH ;
YANG, YZ ;
KILBURN, AE ;
LEE, WH ;
ELLEDGE, SJ .
GENES & DEVELOPMENT, 1993, 7 (04) :555-569
[7]  
Edwards DN, 1997, DEVELOPMENT, V124, P3855
[8]   Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia [J].
Fox, JW ;
Lamperti, ED ;
Eksioglu, YZ ;
Hong, SE ;
Feng, YY ;
Graham, DA ;
Scheffer, IE ;
Dobyns, WB ;
Hirsch, BA ;
Radtke, RA ;
Berkovic, SF ;
Huttenlocher, PR ;
Walsh, CA .
NEURON, 1998, 21 (06) :1315-1325
[9]   A transmembrane domain-derived peptide inhibits D1 dopamine receptor function without affecting receptor oligomerization [J].
George, SR ;
Lee, SP ;
Varghese, G ;
Zeman, PR ;
Seeman, P ;
Ng, GYK ;
O'Dowd, BF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (46) :30244-30248
[10]   Dopamine D1 and adenosine A1 receptors form functionally interacting heteromeric complexes [J].
Ginés, S ;
Hillion, J ;
Torvinen, M ;
Le Crom, S ;
Casadó, V ;
Canela, EI ;
Rondin, S ;
Lew, JY ;
Watson, S ;
Zoli, M ;
Agnati, LF ;
Vernier, P ;
Lluis, C ;
Ferré, S ;
Fuxe, K ;
Franco, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (15) :8606-8611