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446 items found for " myeloid cells"
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- Sweet taste receptor agonists attenuate macrophage IL‐1β expression and eosinophilic inflammation...
attenuate macrophage IL‐1β expression and eosinophilic inflammation linked to autophagy deficiency in myeloid cells "Background Eosinophilic inflammation is a hallmark of refractory chronic rhinosinusitis (CRS Autophagy deficiency in myeloid cells plays a causal role in eosinophilic CRS (ECRS) via macrophage IL trehalose and saccharin on macrophage IL‐1β production and eosinophilia in the mouse model of ECRS with myeloid cell‐specific autophagy‐related gene 7 ( Atg7 ) deletion.
- GPR84 signaling promotes intestinal mucosal inflammation via enhancing NLRP3 inflammasome activation
medium-chain free fatty acid receptor GPR84 is a G protein-coupled receptor primarily expressed in myeloid cells that constitute the innate immune system, including neutrophils, monocytes, and macrophages in These results define a unique role of GPR84 in innate immune cells and intestinal inflammation, and suggest
- 📰 GPCR Weekly News, January 15 to 21, 2024
podocytopathy in kidney disease Hepatocyte GPCR signaling regulates IRF3 to control hepatic stellate cell transdifferentiation GPCRs in Oncology and Immunology The orphan G protein-coupled receptor 141 expressed in myeloid cells functions as an inflammation suppressor Methods & Updates in GPCR Research G-Protein Coupled Receptor with advanced gastroenteropancreatic neuroendocrine tumors Neurocrine Biosciences Announces Conference Call
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- Activation of orphan receptor GPR132 induces cell differentiation in acute myeloid leukemia
< GPCR News < GPCRs in Oncology and Immunology Activation of orphan receptor GPR132 induces cell differentiation in acute myeloid leukemia Published date November 1, 2022 Abstract Blocked cellular differentiation is a critical pathologic hallmark of acute myeloid leukemia (AML). Here, we showed that genetic activation of the orphan GPCR GPR132 significantly induced cell differentiation We further showed that the combination of 8GL and an mTOR inhibitor synergistically elicited AML cell
- Mutation Patterns Predict Drug Sensitivity in Acute Myeloid Leukemia
< GPCR News < GPCRs in Oncology and Immunology Mutation Patterns Predict Drug Sensitivity in Acute Myeloid Experimental design: We performed targeted sequencing, high-throughput drug screening, and single-cell genomic profiling on leukemia cell samples derived from patients with AML. The application of single-cell genomic sequencing unveiled the co-occurrence of variants at the individual cell level, highlighting the presence of distinct subclones within patients with AML.
- S1P Signaling Genes as Prominent Drivers of BCR-ABL1-Independent Imatinib Resistance and Six Herbal Compounds as Potential Drugs for Chronic Myeloid Leukemia
of BCR-ABL1-Independent Imatinib Resistance and Six Herbal Compounds as Potential Drugs for Chronic Myeloid Leukemia Published date July 1, 2024 Abstract "Imatinib (IM), a breakthrough in chronic myeloid leukemia Functional annotation revealed their roles in critical cellular processes such as proliferation and GPCR , leukemia Source Contribute to the GPCR News Coming soon Become a Contributor Classified GPCR News Call