Intracellular trafficking of angiotensin II and its AT(1) and AT(2) receptors: Evidence for selective sorting of receptor and ligand

被引:202
作者
Hein, L
Meinel, L
Pratt, RE
Dzau, VJ
Kobilka, BK
机构
[1] UNIV WURZBURG, DEPT PHARMACOL, WURZBURG, GERMANY
[2] HARVARD UNIV, BRIGHAM & WOMENS HOSP, SCH MED, DEPT MED, BOSTON, MA 02115 USA
[3] STANFORD UNIV, SCH MED, HOWARD HUGHES MED INST, FALK CARDIOVASC RES CTR, STANFORD, CA 94305 USA
[4] STANFORD UNIV, SCH MED, HOWARD HUGHES MED INST, DEPT MED, STANFORD, CA 94305 USA
关键词
D O I
10.1210/me.11.9.1266
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Angiotensin II (Ang II) binds to two different receptor subtypes, AT(1) and AT(2) receptors, In many cases, receptor stimulation by Ang II is followed by a rapid desensitization of the intracellular signal transduction and a decrease in cell surface receptor number, The present study was designed to examine by immunofluorescence microscopy the cellular trafficking pathways of Ang II and its A(1a) and AT(2) receptors in human embryonal kidney 293 cells stably expressing these receptor subtypes, Fluorescently labeled Ang II and AT(1a) receptors were rapidly internalized into endosomes. AT(2) receptors were localized in the plasma membrane and did not undergo endocytosis upon agonist stimulation, After removal of agonist, AT(1a) receptors recycled to the plasma membrane, whereas fluorescently labeled Ang II was targeted to the lysosomal pathway, Even though no further loss of surface receptor was measurable by ligand binding at steady state, fluorescein-Ang II was continuously internalized, and cycling of receptor between endosomal vesicles and the plasma membrane was detected by antibody feeding, These experiments provide evidence for subtype-specific receptor sorting and internalization of Ang II and its AT(1a) receptor as a receptor-ligand complex, and they suggest that the sequestration of receptors into endosomes is in dynamic equilibrium with receptor cycling to the plasma membrane, Finally, internalization of AT(1a) receptors and Ang II persists after desensitization mechanisms have attenuated Ca2+ and inositol 1,4,5-trisphosphate signaling.
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页码:1266 / 1277
页数:12
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