Abstract
Stable and inducible expression of human metabotropic glutamate receptor types 2, 5, and 8 was achieved in HEK293 cells using the ecdysone inducible system. Treatment of the respective cell lines with ponasterone A resulted in time- and concentration-dependent induction of receptor expression. In all cases, the functional activation of receptors was determined by measuring increases in intracellular calcium. The physiologically Gα1- coupled receptors mGluR2 and mGluR8 were successfully coupled to phospholipase C activation using the chimeric G protein Gαq/o. The pharmacological properties of recombinant receptors were characterized and proved to be similar to native receptors. Our data suggest that the ecdysone system has a number of characteristics that make it well suited for expressing mGluRs and that the combined use of this system and chimeric G proteins allows receptors to be characterized using a rapid and straightforward Ca2+ assay.
| Original language | English |
|---|---|
| Pages (from-to) | 841-848 |
| Number of pages | 8 |
| Journal | Journal of Biomolecular Screening |
| Volume | 10 |
| Issue number | 8 |
| DOIs | |
| Publication status | Published - Dec 2005 |
| Externally published | Yes |
Keywords
- Chimeric G proteins
- Inducible expression
- Metabotropic glutamate receptors
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