共 207 条
Regulation of receptor trafficking by GRKs and arrestins
被引:508
作者:

Moore, Catherine A. C.
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机构:
Thomas Jefferson Univ, Dept Biochem & Mol Biol, Philadelphia, PA 19107 USA Thomas Jefferson Univ, Dept Biochem & Mol Biol, Philadelphia, PA 19107 USA

Milano, Shawn K.
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h-index: 0
机构:
Thomas Jefferson Univ, Dept Biochem & Mol Biol, Philadelphia, PA 19107 USA Thomas Jefferson Univ, Dept Biochem & Mol Biol, Philadelphia, PA 19107 USA

Benovic, Jeffrey L.
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机构:
Thomas Jefferson Univ, Dept Biochem & Mol Biol, Philadelphia, PA 19107 USA Thomas Jefferson Univ, Dept Biochem & Mol Biol, Philadelphia, PA 19107 USA
机构:
[1] Thomas Jefferson Univ, Dept Biochem & Mol Biol, Philadelphia, PA 19107 USA
关键词:
GPCR;
endocytosis;
internalization;
sorting;
D O I:
10.1146/annurev.physiol.69.022405.154712
中图分类号:
Q4 [生理学];
学科分类号:
071003 ;
摘要:
To ensure that extracellular stimuli are translated into intracellular signals of appropriate magnitude and specificity most signaling cas, cades are tightly regulated. One of the major mechanisms involved in the regulation of G protein-coupled receptors (GPCRs) involves their endocytic trafficking. GPCR endocytic trafficking entails the targeting of receptors to discrete endocytic sites at the plasma membrane, followed by receptor internalization and intracellular sorting. This regulates the level of cell surface receptors, the sorting of receptors to degradative or recycling pathways, and in some cases the specific signaling pathways. In this chapter we discuss the mechanisms that regulate receptor endocytic trafficking, emphasizing the role of GPCR kinases (GRKs) and arrestins in this process.
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页码:451 / 482
页数:32
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