DARPP-32 and phosphatase inhibitor-1, two structurally related inhibitors of protein phosphatase-1, are both present in striatonigral neurons.

TitleDARPP-32 and phosphatase inhibitor-1, two structurally related inhibitors of protein phosphatase-1, are both present in striatonigral neurons.
Publication TypeJournal Article
Year of Publication1988
AuthorsNairn AC, Hemmings HC, Walaas SI, Greengard P
JournalJ Neurochem
Volume50
Issue1
Pagination257-62
Date Published1988 Jan
ISSN0022-3042
KeywordsAnimals, Basal Ganglia, Carrier Proteins, Corpus Striatum, Dopamine and cAMP-Regulated Phosphoprotein 32, Electrophoresis, Polyacrylamide Gel, Intracellular Signaling Peptides and Proteins, Kainic Acid, Male, Muscles, Nerve Tissue Proteins, Neurons, Phosphoproteins, Phosphorylation, Proteins, Rats, Rats, Inbred Strains, Substantia Nigra
Abstract

DARPP-32 (dopamine- and cyclic AMP-regulated phosphoprotein of Mr = 32,000) and phosphatase inhibitor-1, two previously characterized inhibitors of protein phosphatase-1, were identified in both the neostriatum and the substantia nigra. Phosphatase inhibitor-1 was partially purified from bovine caudate nucleus and found to be distinct from DARPP-32 in some of its biochemical properties. The neuronal localization of DARPP-32 and phosphatase inhibitor-1 within the rat neostriatum and substantia nigra was investigated by studying the effects of kainic acid. Injection into the neostriatum of kainic acid, which destroys striatonigral neurons and striatonigral fibers, decreased the amounts of DARPP-32 and phosphatase inhibitor-1 to the same extent, both in the lesioned neostriatum and in the ipsilateral substantia nigra. The specific activity of protein phosphatase-1 in the neostriatum was unaffected by kainic acid. The results indicate that, in rat brain, DARPP-32 and phosphatase inhibitor-1 are both present in striatal neurons and in striatonigral fibers, and that they probably coexist in at least a subpopulation of striatonigral neurons. In contrast, protein phosphatase-1 does not appear to be enriched in any specific neuronal subpopulation in the neostriatum.

Alternate JournalJ. Neurochem.
PubMed ID3335843
Grant ListMH-40899 / MH / NIMH NIH HHS / United States