The expression patterns of RGS transcripts in platelets

Sung Dae Kim, Hye Jin Sung, Sun Kyu Park, Tae Wan Kim, Seung Chun Park, Sang Keun Kim, Jae Youl Cho, Man Hee Rhee

Research output: Contribution to journalArticlepeer-review

34 Scopus citations

Abstract

Regulators of G protein signalling (RGS) are involved in the negative regulation of cell activation processes and are involved in the pathophysiology of cardiovascular diseases. To get some further evidence for a role of RGS proteins in platelets, we determined the expression profile of RGS-specific mRNA in rat platelets using reverse transcription-polymerase chain reaction (RT-PCR) with a poly dT18 primer and transcript-specific primers. We found that RGS2, RGS3, RGS5, RGS6, RGS10, RGS14, RGS16 and RGS18, Leukemia-associated Rho-GEF factor (LARG), and Gα interacting protein (GAIP) were differentially expressed in platelets. The highest expression rate was found for RGS18 (about 1.3 fold when compared to GAPDH), followed by LARG, RGS6, RGS10 and RGS16 (0.7 to 0.95), whereas expression rates for RGS2, RGS3, RGS5, RGS14, and GAIP were in a range of 0.1 to 0.3. Our results suggest that G-protein-coupled receptor-mediated signalling in platelet may be regulated mainly by RGS 18, 16, 10, 6, and LARG.

Original languageEnglish
Pages (from-to)493-497
Number of pages5
JournalPlatelets
Volume17
Issue number7
DOIs
StatePublished - 1 Nov 2006

Keywords

  • Gene expression
  • Platelets
  • RGS
  • RT-PCR

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