Journal article
Adenylyl cyclase interaction with the D2 dopamine receptor family; Differential coupling to Gi, Gz, and Gs
Cellular and Molecular Neurobiology, Vol.19(5), pp.653-664
Oct/1999
Abstract
1. The D2-type dopamine receptors are thought to inhibit adenylyl cyclase (AC), via coupling to pertussis toxin (PTX)-sensitive G proteins of the Gi family. We examined whether and to what extent the various D2 receptors (D-2S, D-2L, D-3S, D-3L, and D-4) couple to the PTX-insensitive G protein Gz, to produce inhibition of AC activity. 2. COS-7 cells were transiently transfected with the individual murine dopamine receptors alone, as well as together with the Lu subunit of Gz. PTX treatment was employed to inactivate endogenous alpha i, and coupling to Gi and Gz was estimated by measuring the inhibition of cAMP accumulation induced by quinpirole, in forskolin-stimulated cells. 3. D-2S or D-2L receptors can couple to the same extent to Gi and to Gz. The D-4 dopamine receptor couples preferably to Gz, resulting in about 60% quinpirole-induced inhibition of cAMP accumulation. The D-3S, and D-3L receptor isoforms couple slightly to Gz and result in 15 and 30% inhibition of cAMP accumulation, respectively. 4. We have demonstrated for the first time that the two D-3 receptor isoforms, and not any of the other D2 receptor subtypes, also couple to Gs in both COS-7 and CHO transfected cells, in the presence of PTX. 5. Thus, the differential coupling of the D2 dopamine receptor subtypes to various G proteins may add another aspect to the diversity of dopamine receptor function.
Details
- Title
- Adenylyl cyclase interaction with the D2 dopamine receptor family; Differential coupling to Gi, Gz, and Gs
- Creators
- J Obadiah (null)T Avidor-Reiss (null)CS Fishburn (null)Shari Carmon (null) - The Weizmann Institute of ScienceM Bayewitch (null)Zvi Vogel (null) - The Weizmann Institute of ScienceShai Fuchs (null) - 972WIS_INST___111B Levavi-Sivan (null)
- Resource Type
- Journal article
- Publication Details
- Cellular and Molecular Neurobiology, Vol.19(5), pp.653-664; Oct/1999
- Number of pages
- 12
- Language
- English
- DOI
- https://doi.org/10.1023/A:1006988603199
- Record Identifier
- 993266340803596
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