| Literature DB >> 19782129 |
Robin S Gill1, Marilyn S Hsiung, Chi S Sum, Natalie Lavine, Stewart D Clark, Hubert H M Van Tol.
Abstract
Dopamine receptors are GPCRs that play important roles in locomotion, reward, and cognitive processes. Previously, we demonstrated that this receptor transactivates PDGFRbeta to modulate ERK1/2 and NMDA receptor activity. Downregulation of maturely glycosylated PDGFRbeta by prolonged exposure to PDGF-BB eliminated PDGF-BB-mediated ERK1/2 activation. The DRD4-mediated ERK1/2 response was only partially blunted by PDGF-BB-mediated downregulation, but remained sensitive to the PDGFRbeta kinase inhibitor tyrphostin A9. Tunicamycin prevented the N-linked glycosylation and maturation of PDGFRbeta as well as its activation by PDGF-BB. However, upon tunicamycin treatment, DRD4 continued to signal to ERK1/2 in a tyrphostin A9-sensitive manner. Collectively, our observations indicate that DRD4, unlike PDGF-BB, can activate a pool of intracellularly located PDGFRbeta.Entities:
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Year: 2009 PMID: 19782129 DOI: 10.1016/j.cellsig.2009.09.031
Source DB: PubMed Journal: Cell Signal ISSN: 0898-6568 Impact factor: 4.315