The topic of the original funded grant proposal was phosphoinositide regulation of the heat- and capsaicin sensitive TRPV1, and the cold- and menthol-sensitive TRPM8 channels. The current renewal proposal continues to study phosphoinositide regulation of TRPV1, and addresses an important unsolved problem, brought to light by a recent higher resolution structure in lipid nanodiscs, which found that the capsaicin/vanilloid binding site is occupied by a phosphoinositide, and proposed that it stabilizes the channel in the resting state, and vanilloids activate TRPV1 by replacing the lipid. PI(4,5)P2 and PI(4)P however are well established positive cofactors/regulators of TRPV1, which is difficult to reconcile with this model. The exact nature of the phosphoinositide lipid, however, is not well resolved in the structure.
In Aim1 we will elucidate the nature of the phosphoinositide in the vanilloid binding site, using the combination of computational modeling, site directed mutagenesis, whole cell and excised patch electrophysiology and planar lipid bilayers. The TRPM3 ion channel is expressed in Dorsal Root Ganglion (DRG) neurons; its genetic deletion in mice results in altered sensitivity to noxious heat. TRPM3 is activated by heat, and chemical agonists, such as Pregnenolone Sulphate (PregS) and CIM0216. We found that this channel requires phosphoinositides for activity, and we also found that agonists of phospholipase C (PLC)-coupled receptors inhibit TRPM3. This inhibition, however, was not alleviated by intracellular delivery of excess PI(4,5)P2, and was reduced by a protein that binds the ?? subunits of heterotrimeric G-proteins (G?? sink). This finding points to the dominance of G?? signaling over PLC activation in regulating TRPM3. Activation of Gi-coupled receptors that do not activate PLC also robustly inhibited TRPM3 activity, and the effect was reduced by G?? sinks. Co-expression of G?? in intact cells, and application of purified G?? to excised inside-out patches also inhibited TRPM3, and we detected biochemical interaction between TRPM3 and G? by co-immunoprecipitation. These data suggest that G?? subunits are direct negative regulators of TRPM3. We also found that activation of endogenous Gi- coupled GABAB and opioid receptors inhibited PregS-induced Ca2+ signals in DRG neurons.
In Aims 2 and 3, we will test predictions of our model of TRPM3 regulation, and elucidate the molecular determinants of this effect using a combination of molecular biology, patch clamp, planar lipid bilayer, skin-nerve electrophysiology, fluorescence-based cellular imaging techniques, and animal behavior.

Public Health Relevance

Chronic pain is an unmet medical need; associated costs have been estimated in the United States at hundreds billions of dollars annually. Intense heat causes pain, and hypersensitivity to thermal stimuli is a major symptom in chronic pain. We study the molecular regulation of TRPV1 and TRPM3, two important noxious heat sensing ion channels, and our work has the potential to lead to better therapeutic strategies against pain.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS055159-12
Application #
9927674
Study Section
Biophysics of Neural Systems Study Section (BPNS)
Program Officer
Silberberg, Shai D
Project Start
2007-07-01
Project End
2023-05-31
Budget Start
2020-06-01
Budget End
2021-05-31
Support Year
12
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Rutgers University
Department
Pharmacology
Type
Schools of Medicine
DUNS #
078795851
City
Newark
State
NJ
Country
United States
Zip Code
07103
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Kasimova, Marina A; Yazici, Aysenur Torun; Yudin, Yevgen et al. (2018) A hypothetical molecular mechanism for TRPV1 activation that invokes rotation of an S6 asparagine. J Gen Physiol 150:1554-1566
Beckerman, Pazit; Bi-Karchin, Jing; Park, Ae Seo Deok et al. (2017) Transgenic expression of human APOL1 risk variants in podocytes induces kidney disease in mice. Nat Med 23:429-438
Badheka, Doreen; Yudin, Yevgen; Borbiro, Istvan et al. (2017) Inhibition of Transient Receptor Potential Melastatin 3 ion channels by G-protein ?? subunits. Elife 6:
Elokely, Khaled; Velisetty, Phanindra; Delemotte, Lucie et al. (2016) Understanding TRPV1 activation by ligands: Insights from the binding modes of capsaicin and resiniferatoxin. Proc Natl Acad Sci U S A 113:E137-45
Velisetty, Phanindra; Borbiro, Istvan; Kasimova, Marina A et al. (2016) A molecular determinant of phosphoinositide affinity in mammalian TRPV channels. Sci Rep 6:27652
Rohacs, Tibor (2016) Phosphoinositide signaling in somatosensory neurons. Adv Biol Regul 61:2-16
Carnevale, Vincenzo; Rohacs, Tibor (2016) TRPV1: A Target for Rational Drug Design. Pharmaceuticals (Basel) 9:
Yudin, Yevgen; Lutz, Brianna; Tao, Yuan-Xiang et al. (2016) Phospholipase C ?4 regulates cold sensitivity in mice. J Physiol 594:3609-28
Borbiro, Istvan; Badheka, Doreen; Rohacs, Tibor (2015) Activation of TRPV1 channels inhibits mechanosensitive Piezo channel activity by depleting membrane phosphoinositides. Sci Signal 8:ra15

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