Receptor recruitment:: A mechanism for interactions between G protein-coupled receptors

被引:62
作者
Holtbäck, U
Brismar, H
DiBona, GF
Fu, M
Greengard, P
Aperia, A
机构
[1] Astrid Lindgrens Childrens Hosp, Dept Women & Childrens Hlth, Karolinska Inst, S-17176 Stockholm, Sweden
[2] Univ Iowa, Coll Med, Dept Internal Med, Iowa City, IA 52242 USA
[3] Univ Iowa, Coll Med, Dept Physiol, Iowa City, IA 52242 USA
[4] Gothenburg Univ, Wallenberg Lab, S-41345 Gothenburg, Sweden
[5] Rockefeller Univ, Mol & Cellular Neurosci Lab, New York, NY 10021 USA
关键词
D O I
10.1073/pnas.96.13.7271
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
There is a great deal of evidence for synergistic interactions between G protein-coupled signal transduction pathways in various tissues. As two specific examples, the potent effects of the biogenic amines norepinephrine and dopamine on sodium transporters and natriuresis can be modulated by neuropeptide Y and atrial natriuretic peptide, respectively. Here, we report, using a renal epithelial cell line, that both types of modulation involve recruitment of receptors from the interior of the cell to the plasma membrane. The results indicate that recruitment of G protein-coupled receptors may be a ubiquitous mechanism for receptor sensitization and may play a role in the modulation of signal transduction comparable to that of the well established phenomenon of receptor endocytosis and desensitization.
引用
收藏
页码:7271 / 7275
页数:5
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