Search Results
15 items found for "GRK"
- Combinatorial depletions of G-protein coupled receptor kinases in immune cells identify pleiotropic and cell type-specific functions
type-specific functions Published date November 1, 2022 Abstract G-protein coupled receptor kinases (GRKs However, there is growing evidence that GRKs can also control cellular functions beyond GPCR regulation Immune cells commonly express two to four members of the GRK family (GRK2, GRK3, GRK5, GRK6) simultaneously In particular, we are missing comprehensive studies comparing the role of this GRK interplay for (a) To address this issue, we generated mouse models of single, combinatorial and complete GRK knockouts
- Chemoattractant receptor signaling in humoral immunity
After ligand binding, GPCRs are phosphorylated by different GPCR kinases (GRKs) at distinct sites on However, the molecular mechanisms by which individual GRKs are selectively targeted to GPCRs have been domain-containing (COMMD) 3 and 8 (COMMD3/8 complex) functions as an adaptor that recruits a specific GRK Authors Taiichiro Shirai , Akiko Nakai , Kazuhiro Suzuki Tags B cell migration , COMMD3/8 complex , GRK
- Ep 112 with Julia Gardner
She recently led a project that demonstrated the GPCR kinases (GRKs) can translocate to endosomes, and that the subcellular localization of the GRKs affects a GPCR's biased signaling profile.
- Ep 132 with Dr. Richard Premont
initial project to identify and clone taste receptors was unsuccessful, but led to the identification of GRK5 and continued focus on GRKs (particularly GRKs 4,5,6) and arrestins as GPCR regulators and as mediators regulation of G protein-coupled receptor signaling particularly by the G protein-coupled receptor kinase (GRK
- Ep 130 with Dr. Richard Premont
initial project to identify and clone taste receptors was unsuccessful, but led to the identification of GRK5 and continued focus on GRKs (particularly GRKs 4,5,6) and arrestins as GPCR regulators and as mediators regulation of G protein-coupled receptor signaling particularly by the G protein-coupled receptor kinase (GRK
- Ep 133 with Dr. Richard Premont
initial project to identify and clone taste receptors was unsuccessful, but led to the identification of GRK5 and continued focus on GRKs (particularly GRKs 4,5,6) and arrestins as GPCR regulators and as mediators regulation of G protein-coupled receptor signaling particularly by the G protein-coupled receptor kinase (GRK
- Ep 131 with Dr. Richard Premont
initial project to identify and clone taste receptors was unsuccessful, but led to the identification of GRK5 and continued focus on GRKs (particularly GRKs 4,5,6) and arrestins as GPCR regulators and as mediators regulation of G protein-coupled receptor signaling particularly by the G protein-coupled receptor kinase (GRK
- Structure-based discovery of functionally selective 5-HT1A receptor agonists
has been spokesman of the Research Training Group "Medicinal Chemistry of Selective GPCR Ligands" (GRK
- Ep 111 with Chloe Hicks
differential signaling outputs of biased agonists, and demonstrating the ligand specificity behind GRK
- Distinct Activation Mechanisms of CXCR4 and ACKR3 Revealed by Single-Molecule Analysis of their Conformational Landscapes
By contrast, ACKR3 recruits GPCR kinases (GRKs) and β-arrestins and promiscuously responds to CXCL12,
- DANGER Signals Activate G-Protein Receptor Kinases Suppressing Neutrophil Function and Predisposing to Infection After Tissue Trauma
GPCR kinases (GRKs) can regulate GPCR activation. Heme also activates GRK2. GRK2 inhibitors like paroxetine restore functions. GRK2 activation via TLR9 prevented actin reorganization, implicating histone deacetylases (HDACs). and a novel TLR-activated GRK2 pathway impairing cytoskeletal organization. Simultaneous GRK2/HDAC inhibition rescues susceptibility to infection after tissue injury.
- Ep 152 with Dr Arthur Christopoulos
They discussed various modulatory elements, such as RAMPs, G proteins, and GRKs, with Arthur recounting
- miR-19a may function as a biomarker of oral squamous cell carcinoma (OSCC) by regulating the signaling pathway of miR-19a/GRK6/GPCRs/PKC in a Chinese population
as a biomarker of oral squamous cell carcinoma (OSCC) by regulating the signaling pathway of miR-19a/GRK6 Wang , Danhua Ma , He Zhang , Jiayan Fan , Hongyan Gao , Xinyu Xia , Wei Wu , Yuyuan Shi Tags GPCR , GRK6
- Prediction of survival and immunotherapy response by the combined classifier of G protein-coupled receptors and tumor microenvironment in melanoma
analysis and luciferase assays were performed to establish a potential signaling pathway of miR-19a/GRK6 Results: We found that miR-19a, GPR39 mRNA and PKC mRNA were upregulated while GRK6 mRNA was downregulated Moreover, in silico analysis confirmed a potential binding site of miR-19a on the 3'UTR of GRK6 mRNA, and the subsequent luciferase assays confirmed the molecular binding between GRK6 and miR-19a. We further identified that the over-expression of miR-19a could regulate the signaling between GRK6,
- Unveiling Non-Canonical Functions for Gαq Signaling Pathways
Ribas has also described a new protective role of G protein-coupled receptor kinase 2 (GRK2), a known