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Science 22 April 2005: Vol. 308. no. 5721, pp. 512 - 517 DOI: 10.1126/science.1109237
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Review
Transduction of Receptor Signals by ß-Arrestins
Robert J. Lefkowitz1,2* and
Sudha K. Shenoy2
The transmission of extracellular signals to the interior of the cell is a function of plasma membrane receptors, of which the seven transmembrane receptor family is by far the largest and most versatile. Classically, these receptors stimulate heterotrimeric G proteins, which control rates of generation of diffusible second messengers and entry of ions at the plasma membrane. Recent evidence, however, indicates another previously unappreciated strategy used by the receptors to regulate intracellular signaling pathways. They direct the recruitment, activation, and scaffolding of cytoplasmic signaling complexes via two multifunctional adaptor and transducer molecules, ß-arrestins 1 and 2. This mechanism regulates aspects of cell motility, chemotaxis, apoptosis, and likely other cellular functions through a rapidly expanding list of signaling pathways.
1 Howard Hughes Medical Institute, Durham, NC 27710, USA.
2 Duke University Medical Center, Durham, NC 27710, USA.
* To whom correspondence should be addressed. E-mail: lefko001{at}receptor-biol.duke.edu
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Science
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PNAS
104, 16657-16662
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282, 29549-29562
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Am J Physiol Endocrinol Metab
293, E932-E940
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Cardiovasc Res
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- Chemoattraction of Macrophages, T Lymphocytes, and Mast Cells Is Evolutionarily Conserved within the Human {alpha}-Defensin Family.
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FASEB J
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Cardiovasc Res
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- Molecular Scaffolds Regulate Bidirectional Crosstalk Between Wnt and Classical Seven-Transmembrane Domain Receptor Signaling Pathways.
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Sci. STKE
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- Membrane Glycoprotein M6a Interacts with the {micro}-Opioid Receptor and Facilitates Receptor Endocytosis and Recycling.
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- The Active Conformation of beta-Arrestin1: DIRECT EVIDENCE FOR THE PHOSPHATE SENSOR IN THE N-DOMAIN AND CONFORMATIONAL DIFFERENCES IN THE ACTIVE STATES OF beta-ARRESTINS1 AND -2.
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PNAS
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- Oxyntomodulin Differentially Affects Glucagon-Like Peptide-1 Receptor beta-Arrestin Recruitment and Signaling through G{alpha}.
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Am J Physiol Regulatory Integrative Comp Physiol
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- Differential effects of beta-arrestins on the internalization, desensitization and ERK1/2 activation downstream of protease activated receptor-2.
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Am J Physiol Cell Physiol
293, C346-C357
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- Calcium-Sensing Receptor Endocytosis Links Extracellular Calcium Signaling to Parathyroid Hormone-Related Peptide Secretion via a Rab11a-Dependent and AMSH-Sensitive Mechanism.
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- Modified Receptor Internalization upon Coexpression of 5-HT1B Receptor and 5-HT2B Receptors.
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- 5-Hydroxytryptamine4 Receptor Activation of the Extracellular Signal-regulated Kinase Pathway Depends on Src Activation but Not on G Protein or beta-Arrestin Signaling.
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Mol. Biol. Cell
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