Differential distribution of PDE4D splice variant mRNAs in rat brain suggests association with specific pathways and presynaptical localization

被引:49
作者
Miró, X
Pérez-Torres, S
Puigdomènech, P
Palacios, JM
Mengod, G
机构
[1] CSIC, IDIBAPS, IIBB, Dept Neurochem, Barcelona 08036, Spain
[2] CSIC, Cid, Inst Mol Biol, Dept Mol Genet, E-08034 Barcelona, Spain
关键词
in situ hybridization; emesis; area postrema; depression; serotonergic cells; rolipram;
D O I
10.1002/syn.10100
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
cAMP plays an important role as a second-messenger molecule controlling multiple cellular processes. Its hydrolysis provides an important mechanism by which cAMP levels are regulated. This is performed by a large multigene family of cyclic nucleotide phosphodiesterases (PDEs). Members of the PDE4 enzyme family are selectively inhibited by rolipram. Five different mRNA splice forms for PDE4D have been isolated. Here, we analyzed the regional distribution of the mRNAs coding for the splice variants PDE4D1, PDE4D2, PDE4D3, PDE4D4, and PDE4D5 in the rat brain by in situ hybridization histochemistry using specific radiolabeled oligonucleotides. We found that all five splice variants showed a distinct distribution pattern and, in some cases, in association with specific brain pathways. The most relevant differences were in hippocampal formation, medial habenula, basal ganglia, and area postrema, at both the regional and cellular level. The dorsal and median raphe nuclei exclusively contained PDE4D2 mRNA transcripts, probably located on serotonergic cells. PDE4D1 mRNA was expressed in some white matter cells. PDE4D1 and PDE4D2 mRNA splice forms presented a similar distribution in the area postrema, whereas for PDE4D4 and PDE4D5 the cellular distribution presented a complementary pattern. The differential expression of PDE4D mRNA splice variants in the area postrema is consistent with their possible involvement in emesis control and suggests new molecular targets for a more selective drug design. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:259 / 269
页数:11
相关论文
共 59 条
[1]
Andres KH, 1999, J COMP NEUROL, V407, P130, DOI 10.1002/(SICI)1096-9861(19990428)407:1<130::AID-CNE10>3.0.CO
[2]
2-8
[3]
Sub-family selective actions in the ability of Erk2 MAP kinase to phosphorylate and regulate the activity of PDE4 cyclic AMP-specific phosphodiesterases [J].
Baillie, GS ;
MacKenzie, SJ ;
McPhee, I ;
Houslay, MD .
BRITISH JOURNAL OF PHARMACOLOGY, 2000, 131 (04) :811-819
[4]
The unique N-terminal domain of the cAMP phosphodiesterase PDE4D4 allows for interaction with specific SH3 domains [J].
Beard, MB ;
O'Connell, JC ;
Bolger, GB ;
Houslay, MD .
FEBS LETTERS, 1999, 460 (01) :173-177
[6]
A FAMILY OF HUMAN PHOSPHODIESTERASES HOMOLOGOUS TO THE DUNCE LEARNING AND MEMORY GENE-PRODUCT OF DROSOPHILA-MELANOGASTER ARE POTENTIAL TARGETS FOR ANTIDEPRESSANT DRUGS [J].
BOLGER, G ;
MICHAELI, T ;
MARTINS, T ;
STJOHN, T ;
STEINER, B ;
RODGERS, L ;
RIGGS, M ;
WIGLER, M ;
FERGUSON, K .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (10) :6558-6571
[7]
Bolger GB, 1997, BIOCHEM J, V328, P539
[8]
BORISON HL, 1953, PHARMACOL REV, V5, P193
[9]
Lipopolysaccharide induces expression of tumour necrosis factor alpha in rat brain: inhibition by methylprednisolone and by rolipram [J].
Buttini, M ;
Mir, A ;
Appel, K ;
Wiederhold, KH ;
Limonta, S ;
GebickeHaerter, PJ ;
Boddeke, HWGM .
BRITISH JOURNAL OF PHARMACOLOGY, 1997, 122 (07) :1483-1489
[10]
EXCITATION OF AREA POSTREMA NEURONS BY TRANSMITTERS, PEPTIDES, AND CYCLIC-NUCLEOTIDES [J].
CARPENTER, DO ;
BRIGGS, DB ;
KNOX, AP ;
STROMINGER, N .
JOURNAL OF NEUROPHYSIOLOGY, 1988, 59 (02) :358-369