The expression patterns of RGS transcripts in platelets

被引:30
作者
Kim, Sung Dae
Sung, Hye Jin
Park, Sun Kyu
Kim, Tae Wan
Park, Seung Chun
Kim, Sang Keun
Cho, Jae Youl
Rhee, Man Hee [1 ]
机构
[1] Kyungpook Natl Univ, Coll Vet Med, Lab Vet Physiol & Signalling, Taegu 702701, South Korea
[2] Chungnam Natl Univ, Coll Vet Med, Taejon 302305, South Korea
[3] Kangweon Natl Univ, Sch Biotechnol & Bioengn, Chunchon 200701, South Korea
关键词
platelets; RGS; gene expression; RT-PCR;
D O I
10.1080/09537100600758123
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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 dT(18) primer and transcript-specific primers. We found that RGS2, RGS3, RGS5, RGS6, RGS10, RGS14, RGS16 and RGS18, Leukemia-associated Rho-GEF factor (LARG), and G alpha 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.
引用
收藏
页码:493 / 497
页数:5
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