Visualization of agonist-induced sequestration and down-regulation of a green fluorescent protein-tagged β2-adrenergic receptor

被引:151
作者
Kallal, L [1 ]
Gagnon, AW [1 ]
Penn, RB [1 ]
Benovic, JL [1 ]
机构
[1] Thomas Jefferson Univ, Kimmel Canc Inst, Dept Microbiol & Immunol, Philadelphia, PA 19107 USA
关键词
D O I
10.1074/jbc.273.1.322
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To date, the visualization of beta(2)-adrenergic receptor (beta(2)AR) trafficking has been largely limited to immunocytochemical analyses of acute internalization events of epitope-tagged receptors in various transfection systems, The development of a beta(2)AR conjugated with green fluorescent protein (beta(2)AR-GFP) provides the opportunity for a more extensive optical analysis of beta(2)AR sequestration, down-regulation, and recycling in cells. Here we demonstrate that stable expression of beta(2)AR-GFP in HeLa cells enables a detailed temporal and spatial analysis of these events, Time dependent colocalization of beta(2)AR-GFP with rhodamine-labeled transferrin and rhodamine-labeled dextran following agonist exposure demonstrates receptor distribution to early endosomes (sequestration) and lysosomes (down-regulation), respectively. The observed temporal distribution of beta(2)AR-GFP was consistent with measures of receptor sequestration and down-regulation generated by radioligand-receptor binding assays. Cells stimulated with different beta-agonists revealed time courses of beta(2)AR-GFP redistribution reflective of the intrinsic activity of each agonist.
引用
收藏
页码:322 / 328
页数:7
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