Expression of human mu-opioid receptor cDNA in CHO cell.
- Author:
Wei LIU
1
;
Hai-Qing DUAN
;
Shu-Qin LI
;
Xiu-Li LIU
;
Zhao-Shan ZHANG
Author Information
1. Beijing Institute of Biotechnology, Beijing 100071, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Brain Chemistry;
CHO Cells;
Cricetinae;
Cricetulus;
DNA, Complementary;
biosynthesis;
genetics;
Humans;
Receptors, Opioid, mu;
biosynthesis;
genetics;
Transfection
- From:
Chinese Journal of Biotechnology
2004;20(3):372-376
- CountryChina
- Language:Chinese
-
Abstract:
Opioid receptor, is classified into three subtypes, mu, kappa and delta, with the mu-type receptor plays important roles in opioid analgesia and opioid addiction. The cDNA encoding mu-type receptor was obtained by RT-PCR from human brain RNA and was cloned into pcDNA3.1(+). The resultant recombinant plasmid pcDNAMORs were transfected into CHO cells by liposome. After PCR identification, the positive clone were treated with agonist and antiagonist were tested for their competence of signal transduction. CHO cells that contained mu-opioid receptor in the expression vector pcDNA3.1(+) acquired naloxone-blockable high-affinity specific binding of morphine and DAMGO. The concentration of cAMP in CHO cells transfected with pcDNAMOR was reduced after binding to morphine and DAMGO, and increased after binding naloxone. These results indicate that the mu-type receptor expreesd on the CHO cell has similar biological property as the nature receptor. The availability of these specific cell lines will facilitate the drug development and promote our understanding the mechanism underlying opiate addiction.
