Research Summary:
Internal membrane compartments as hubs of signaling To function properly, cells and tissue must receive and interpret a large variety of signals. They do so, in part, through signaling receptors, some of which reside on cell surfaces known as plasma membranes. We study adrenergic receptors, which are targets of commonly used medicines including alpha and beta blockers. By developing a new class of sensors that allow for detection and visualization of signaling events in living cells, we made the unexpected finding that signaling cues to cells not only act on cell surface receptors but also on internal cellular compartments. This observation raises numerous questions pertaining to fundamental aspects of cell signaling and suggests that cells have spatially compartmentalized signaling hubs. This basic biological insight has clinical implications as well. For example, certain beta-blockers are known to have differential clinical efficacies but the underlying reasons for these differences are not known. We have found that different beta blockers act on distinct hubs of signaling. Beyond their well-established roles in cardiac physiology, adrenergic receptors regulate a wide variety of important physiologically and behavioral processes. We are using our newly developed tools to investigate the consequences of signaling from internal compartments on a range of cellular, physiological, and behavioral outcomes.
Publications
Subcellular activation of β-adrenergic receptors using a spatially restricted antagonist.
cAMP signaling: a remarkably regional affair.
Selective activation of intracellular β1AR using a spatially restricted antagonist.
Cardiac contraction and relaxation are regulated by distinct subcellular cAMP pools.
The organic cation transporter 2 regulates dopamine D1 receptor signaling at the Golgi apparatus.
Emerging Role of Compartmentalized G Protein-Coupled Receptor Signaling in the Cardiovascular Field.
Genetically Encoding Quinoline Reverses Chromophore Charge and Enables Fluorescent Protein Brightening in Acidic Vesicles.
Functional selectivity of GPCR-directed drug action through location bias.
Retromer Endosome Exit Domains Serve Multiple Trafficking Destinations and Regulate Local G Protein Activation by GPCRs.
The α-Arrestin ARRDC3 Regulates the Endosomal Residence Time and Intracellular Signaling of the β2-Adrenergic Receptor.
Effects of endocytosis on receptor-mediated signaling.
G protein βγ subunits regulate cardiomyocyte hypertrophy through a perinuclear Golgi phosphatidylinositol 4-phosphate hydrolysis pathway.
G protein-coupled receptor (GPCR) signaling via heterotrimeric G proteins from endosomes.
Investigating signaling consequences of GPCR trafficking in the endocytic pathway.
GPCR signaling along the endocytic pathway.
Regulation of constitutive cargo transport from the trans-Golgi network to plasma membrane by Golgi-localized G protein betagamma subunits.
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