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Molecular basis of parathyroid hormone receptor signaling and trafficking: a family B GPCR paradigm
Authors:Jean-Pierre Vilardaga  Guillermo Romero  Peter A Friedman  Thomas J Gardella
Institution:(1) Laboratory for GPCR Biology, Department of Pharmacology and Chemical Biology, School of Medicine, University of Pittsburgh, E1357 Thomas E. Starzl Biochemical Science Tower, 200 Lothrop Street, Pittsburgh, PA 15261, USA;(2) Endocrine Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA
Abstract:The parathyroid hormone (PTH) receptor type 1 (PTHR), a G protein-coupled receptor (GPCR), transmits signals to two hormone systems—PTH, endocrine and homeostatic, and PTH-related peptide (PTHrP), paracrine—to regulate different biological processes. PTHR responds to these hormonal stimuli by activating heterotrimeric G proteins, such as GS that stimulates cAMP production. It was thought that the PTHR, as for all other GPCRs, is only active and signals through G proteins on the cell membrane, and internalizes into a cell to be desensitized and eventually degraded or recycled. Recent studies with cultured cell and animal models reveal a new pathway that involves sustained cAMP signaling from intracellular domains. Not only do these studies challenge the paradigm that cAMP production triggered by activated GPCRs originates exclusively at the cell membrane but they also advance a comprehensive model to account for the functional differences between PTH and PTHrP acting through the same receptor.
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