Blood pressure regulation relies on the ability of membrane proteins to transduce variations in physical stimuli (e.g., hemodynamic forces) into electrical signals. The transient receptor potential vanilloid 4 (TRPV4) is a pu- tative mechanosensitive Ca2+ channel expressed in endothelial and smooth muscle cells and in perivascular sensory neurons. Although TRPV4 has been implicated in endothelium- and perivascular nerve-dependent vasorelaxation, its precise gating mechanism remains elusive. Three mechanisms have been proposed to activate TRPV4 after mechanical stimulation: 1) downstream of the phospholipase A2 (PLA2)-dependent formation of omega (w)-6 arachidonic acid (AA) and its metabolites, epoxyeicosatrienoic acids (EETs); 2) downstream of purinergic P2Y2 receptor activation, mediated by adenosine triphosphate release; and 3) direct activation by membrane stretch. Our long-term goal is to delineate the mechanisms by which ion channels decode exogenous and endogenous stimuli to regulate cellular function. In this proposal, the overall objective is to establish the molecular basis underlying TRPV4 activation. The central hypothesis is that TRPV4 activation is regulated by the mechanical properties of the membrane via lipid remodeling. The rationale for the proposed research plan is that once the precise mechanism of TRPV4 activation has been elucidated, it will be possible to define strategies that target TRPV4 to control systemic blood pressure. The hypothesis will be tested by pursuing three Specific Aims: 1) Determine the effect of w-6 and w-3 fatty acids on TRPV4 activity in C. elegans; 2) Test the hypothesis that w-3 fatty acid derivatives enhance TRPV4 activity in vascular cells; and 3) Determine how changes in the mechanical properties of the membrane regulates TRPV4 gating. We will leverage genetic, behavioral, functional, biochemical, and biophysical approaches to uncover the contribution of fatty acids and their metabolites to TRPV4 function. The research plan is innovative because it will determine the individual contribution of w-3 and w-6 fatty acids and their eicosanoid derivatives to TRPV4 gating. The proposed research is significant because it is expected to have broad translational importance in targeting TRPV4 to regulate vascular and neuronal function.
The proposed research is relevant to public health because dietary consumption of polyunsaturated fatty acids (PUFAs) is known to prevent cardiovascular diseases; however, the mechanisms and molecular targets of PUFAs and their metabolites remain largely unknown. Members of the transient receptor potential (TRP) channel family act as biological sensors by decoding various physiological cues in the environment to regulate cellular function, including vascular tone. The proposed study is relevant to NIH?s mission because it will provide the molecular basis by which dietary fatty acids modulate TRP channels function in the vascular system.
|Azumaya, Caleigh M; Sierra-Valdez, Francisco; Cordero-Morales, Julio F et al. (2018) Cryo-EM structure of the cytoplasmic domain of murine transient receptor potential cation channel subfamily C member 6 (TRPC6). J Biol Chem 293:10381-10391|
|Sierra-Valdez, Francisco; Azumaya, Caleigh M; Romero, Luis O et al. (2018) Structure-function analyses of the ion channel TRPC3 reveal that its cytoplasmic domain allosterically modulates channel gating. J Biol Chem 293:16102-16114|
|Cordero-Morales, Julio F; Vásquez, Valeria (2018) How lipids contribute to ion channel function, a fat perspective on direct and indirect interactions. Curr Opin Struct Biol 51:92-98|
|Li, Dong; Zou, Xiao-Ying; El-Ayachi, Ikbale et al. (2018) Human Dental Pulp Stem Cells and Gingival Mesenchymal Stem Cells Display Action Potential Capacity In Vitro after Neuronogenic Differentiation. Stem Cell Rev :|
|Sierra-Valdez, Francisco J; Stein, Richard A; Velissety, Phanindra et al. (2018) Purification and Reconstitution of TRPV1 for Spectroscopic Analysis. J Vis Exp :|
|Velisetty, Phanindra; Stein, Richard A; Sierra-Valdez, Francisco J et al. (2017) Expression and Purification of the Pain Receptor TRPV1 for Spectroscopic Analysis. Sci Rep 7:9861|