Important advances have been made in the understanding of the pharmacology of bradykinin receptor. These studies point to a role of the receptor as a powerful hypotensive, proinflammatory mediator. The bradykinin B2 (BKB2) receptor has been identified as an agent in edema, pain and septic shock. At this time little is known of the structural events within the receptor ultimately regulating its functions. Better understanding of the structure/function events could lead to important new therapeutic approaches in dealing with such pathologic states as shock and hypertension. Our results lead us to formulate a working hypothesis stating that receptor uptake and resensitization are linked while receptor desensitization is a separate process. Signal transduction by the receptor is accomplished through a G-protein interaction with motifs within the 2nd, 3rd loops and the C-terminus interacting with the G-protein(s). Phosphorylation within the 2nd IC loop and distal C-terminus initiates receptor uptake. Phosphorylation within the 3rd IC loop initiates desensitization. Resensitization entails dephosphorylation of the receptor. 1. We will investigate receptor function utilizing targeted mutations and chimera exchange. We will continue to test amino acid motif-function relationship. We will explore charge/bulk interactions among distal motifs potentially interactive to produce function and explore the role of phosphorylation of serine/threonine residues in the 2nd and 3rd IC loops and the carboxylic (C) terminus. 2. We will determine regulation of receptor desensitization, resensitization and uptake. We will build on our findings. We will determine if internalization and resensitization are separate or simultaneous events and if uptake is necessary for resensitization. 3. With such procedures as knockout, and G-alpha unit chimera formation, we will determine G-protein/receptor interaction. Because of the evidently predominant BKB2R/Gq interaction we will initially focus on the Gq family with the BKB2 receptor. We will also focus on other subunits such as the G family.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
2R01HL025776-16
Application #
2616992
Study Section
Lung Biology and Pathology Study Section (LBPA)
Project Start
1981-02-01
Project End
2002-07-31
Budget Start
1998-08-01
Budget End
1999-07-31
Support Year
16
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Boston University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
604483045
City
Boston
State
MA
Country
United States
Zip Code
02118
Wilson, Jamie L; Warburton, Rod; Taylor, Linda et al. (2018) Unraveling endothelin-1 induced hypercontractility of human pulmonary artery smooth muscle cells from patients with pulmonary arterial hypertension. PLoS One 13:e0195780
Wilson, Jamie L; Rupasinghe, Chamila; Usheva, Anny et al. (2015) Modulating the dysregulated migration of pulmonary arterial hypertensive smooth muscle cells with motif mimicking cell permeable peptides. Curr Top Pept Protein Res 16:1-17
Wilson, Jamie L; Yu, Jun; Taylor, Linda et al. (2015) Hyperplastic Growth of Pulmonary Artery Smooth Muscle Cells from Subjects with Pulmonary Arterial Hypertension Is Activated through JNK and p38 MAPK. PLoS One 10:e0123662
Yu, Jun; Wilson, Jamie; Taylor, Linda et al. (2015) DNA microarray and signal transduction analysis in pulmonary artery smooth muscle cells from heritable and idiopathic pulmonary arterial hypertension subjects. J Cell Biochem 116:386-97
Yu, Jun; Rupasinghe, Chamila; Wilson, Jamie L et al. (2015) Targeting receptor tyrosine kinases and their downstream signaling with cell-penetrating peptides in human pulmonary artery smooth muscle and endothelial cells. Chem Biol Drug Des 85:586-97
Yao, Chunxiang; Yu, Jun; Taylor, Linda et al. (2015) Protein Expression by Human Pulmonary Artery Smooth Muscle Cells Containing a BMPR2 Mutation and the Action of ET-1 as Determined by Proteomic Mass Spectrometry. Int J Mass Spectrom 378:347-359
Green, Daniel S; Rupasinghe, Chamila; Warburton, Rod et al. (2013) A cell permeable peptide targeting the intracellular loop 2 of endothelin B receptor reduces pulmonary hypertension in a hypoxic rat model. PLoS One 8:e81309
Yatawara, Achani; Wilson, Jamie L; Taylor, Linda et al. (2013) C-terminus of ETA/ETB receptors regulate endothelin-1 signal transmission. J Pept Sci 19:257-62
Yu, Jun; Taylor, Linda; Wilson, Jamie et al. (2013) Altered expression and signal transduction of endothelin-1 receptors in heritable and idiopathic pulmonary arterial hypertension. J Cell Physiol 228:322-9
Wilson, Jamie L; Taylor, Linda; Polgar, Peter (2012) Endothelin-1 activation of ETB receptors leads to a reduced cellular proliferative rate and an increased cellular footprint. Exp Cell Res 318:1125-33

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