Your privacy, your choice

We use essential cookies to make sure the site can function. We also use optional cookies for advertising, personalisation of content, usage analysis, and social media.

By accepting optional cookies, you consent to the processing of your personal data - including transfers to third parties. Some third parties are outside of the European Economic Area, with varying standards of data protection.

See our privacy policy for more information on the use of your personal data.

for further information and to change your choices.

Skip to main content
Fig. 6 | Cellular & Molecular Biology Letters

Fig. 6

From: Transactivation of the EGF receptor as a novel desensitization mechanism for G protein-coupled receptors, illustrated by dopamine D2-like and β2 adrenergic receptors

Fig. 6

Induction of the GPCR desensitization causes the interaction between D2-like receptors. HEK-293 cells were transfected with EGFR-GFP along with FLAG-tagged D2-like receptors. “ + ” and “w/+” represent the cells treated with the corresponding agonist for 5 min and washed/rechallenged, respectively. The cell lysates were immunoprecipitated with FLAG beads. Co-IP/lysate and IP were immunoblotted with antibodies against GFP and FLAG. A FLAG-tagged D2R and D3R were used. Cells were treated with 10 μM of dopamine. **p < 0.01 compared with other groups of the cells expressing D3R or D4R (n = 3). B FLAG-tagged D3R and D4R were used. Cells were treated with 10 μM of dopamine. **p < 0.01 compared with other groups of the cells expressing D3R or D4R (n = 4). C FLAG-tagged WT-D3R and C147K-D3R were used. Cells were treated with 100 nM of quinpirole. **p < 0.01 compared with other groups of the cells expressing WT-D3R or C147K-D3R (n = 4). D FLAG-tagged WT-D2R and K149C-D2R were used. Cells were treated with 10 μM of dopamine. **p < 0.01 compared with other groups of the cells expressing WT-D2R or K149C-D2R (n = 3)

Back to article page