Differential regulation of the Cdk5-dependent phosphorylation sites of inhibitor-1 and DARPP-32 by depolarization

Chan Nguyen, Tomohisa Hosokawa, Mahomi Kuroiwa, Nancy Y. Ip, Akinori Nishi, Shin Ichi Hisanaga, James A. Bibb

Research output: Contribution to journalArticlepeer-review

4 Scopus citations


While cyclin-dependent kinase 5 (Cdk5) is of growing importance to neuronal signaling, its regulation remains relatively unexplored. Examination of the mechanism by which NMDA modulates the phosphorylation of protein phosphatase inhibitor-1 at Ser6 and Ser67 and dopamine- and cAMP-regulated phosphoprotein Mr 32 000 at Thr75 revealed that generalized depolarization, rather than specific activation of NMDA receptors, was sufficient to induce decreases in these Cdk5 sites. Although no evidence for the involvement of the Cdk5 cofactors p35 or p39, or for L- and T-type voltage-gated Ca2+ channels, was found, evaluation of the role of phosphatases and extracellular cations revealed differential regulation of the three sites. NMDA-induced decreases in the phosphorylation of Thr75 of dopamine- and cAMP-regulated phosphoprotein Mr 32 000 required protein phosphatase 1/2A activity and extracellular Ca2+. In contrast, the effects on Ser6 and Ser67 of inhibitor-1 were not cation specific; either Na+ or Ca2+ sufficed. Furthermore, while the decrease in phosphorylation of Ser6 was partially dependent on protein phosphatase 2B, that of Ser67 was independent of the major protein serine/threonine phosphatases, likely indicating the presence of a pathway by which NMDA inhibits Cdk5 activity. Thus, in the striatum the regulation of phosphorylation of Cdk5-dependent sites by NMDA occurs through multiple distinct pathways.

Original languageEnglish (US)
Pages (from-to)1582-1593
Number of pages12
JournalJournal of Neurochemistry
Issue number4
StatePublished - Nov 2007


  • Cyclin-dependent kinase 5
  • Depolarization
  • Dopamine- and cAMP-regulated phosphoprotein
  • N-methyl-d-aspartate
  • Protein phosphatase
  • Protein phosphatase inhibitor-1

ASJC Scopus subject areas

  • Biochemistry
  • Cellular and Molecular Neuroscience


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