Phospholipase D2-dependent inhibition of the nuclear hormone receptor PPARgamma by cyclic phosphatidic acid. - Test2 - elhamkhani - TriplyDB

Phospholipase D2-dependent inhibition of the nuclear hormone receptor PPARgamma by cyclic phosphatidic acid.

Phospholipase D2-dependent inhibition of the nuclear hormone receptor PPARgamma by cyclic phosphatidic acid.

http://www.wikidata.org/entity/Q36246883

about

Mammalian phospholipase D physiological and pathological roles Lipidome in colorectal cancer Revealing a steroid receptor ligand as a unique PPARγ agonist Structural evidence of the species-dependent albumin binding of the modified cyclic phosphatidic acid with cytotoxic properties Potential of Natural Products in the Inhibition of Adipogenesis through Regulation of PPARγ Expression and/or Its Transcriptional Activity Phospholipases D1 and D2 Suppress Appetite and Protect against Overweight Lysophosphatidic acid activates peroxisome proliferator activated receptor-γ in CHO cells that over-express glycerol 3-phosphate acyltransferase-1 The mito-DAMP cardiolipin blocks IL-10 production causing persistent inflammation during bacterial pneumonia Cellular and physiological roles for phospholipase D1 in cancer.Structural determinants of the transient receptor potential 1 (TRPV1) channel activation by phospholipid analogs Lysophosphatidic acid in atherosclerotic diseases Aiming drug discovery at lysophosphatidic acid targets.Phospholipase D toxins of brown spider venom convert lysophosphatidylcholine and sphingomyelin to cyclic phosphates Endogenous ligands for nuclear receptors: digging deeper.Deficiencies of the lipid-signaling enzymes phospholipase D1 and D2 alter cytoskeletal organization, macrophage phagocytosis, and cytokine-stimulated neutrophil recruitment.PTB-associated splicing factor (PSF) is a PPARγ-binding protein and growth regulator of colon cancer cells.The phospholipase A1 activity of lysophospholipase A-I links platelet activation to LPA production during blood coagulation Cyclic phosphatidic acid stimulates cAMP production and inhibits growth in human colon cancer cells.Phospholipase D: enzymology, functionality, and chemical modulation Lipin-1 phosphatidic phosphatase activity modulates phosphatidate levels to promote peroxisome proliferator-activated receptor γ (PPARγ) gene expression during adipogenesis.Pharmacological repression of PPARγ promotes osteogenesis Phosphatidic Acid (PA) can Displace PPARα/LXRα Binding to The EGFR Promoter Causing its Transrepression in Luminal Cancer Cells Alterations in lipid signaling underlie lipodystrophy secondary to AGPAT2 mutations.PPAR γ Networks in Cell Signaling: Update and Impact of Cyclic Phosphatidic Acid.CDP-diacylglycerol synthases regulate the growth of lipid droplets and adipocyte development.Roles for the lipid-signaling enzyme MitoPLD in mitochondrial dynamics, piRNA biogenesis, and spermatogenesis.PLD1 regulates adipogenic differentiation through mTOR - IRS-1 phosphorylation at serine 636/639.Phospholipase D (PLD) drives cell invasion, tumor growth and metastasis in a human breast cancer xenograph model.Take-over: multiple mechanisms of inter-adipocyte communication.Nuclear sphingolipid metabolism.Blocking the peroxisome proliferator-activated receptor (PPAR): an overview.Disentangling biological signaling networks by dynamic coupling of signaling lipids to modifying enzymes.Modes-of-Action Related to Repeated Dose Toxicity: Tissue-Specific Biological Roles of PPAR γ Ligand-Dependent Dysregulation in Nonalcoholic Fatty Liver Disease.Phospholipid regulation of the nuclear receptor superfamily.Release of cyclic phosphatidic acid from gelatin-based hydrogels inhibit colon cancer cell growth and migration.The PTB-Associated Splicing Factor/Peroxisome Proliferator-Activated Receptor Gamma Axis Regulates Autophagosome Formation in Human Pancreatic Cancer Cells.PPARs and lipid ligands in inflammation and metabolism.The Role of PPARγ in the Transcriptional Control by Agonists and Antagonists.Cyclic phosphatidic acid inhibits alkyl-glycerophosphate-induced downregulation of histone deacetylase 2 expression and suppresses the inflammatory response in human coronary artery endothelial cells.A metabolomics strategy for detecting protein-metabolite interactions to identify natural nuclear receptor ligands.

P2860

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P2860

Phospholipase D2-dependent inhibition of the nuclear hormone receptor PPARgamma by cyclic phosphatidic acid.

http://www.wikidata.org/entity/Q36246883

description

2010 nî lūn-bûn

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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2010年论文

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2010年论文

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name

Phospholipase D2-dependent inh ...... a by cyclic phosphatidic acid.

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Phospholipase D2-dependent inh ...... a by cyclic phosphatidic acid.

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type

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Phospholipase D2-dependent inh ...... a by cyclic phosphatidic acid.

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Phospholipase D2-dependent inh ...... a by cyclic phosphatidic acid.

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Phospholipase D2-dependent inh ...... a by cyclic phosphatidic acid.

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Phospholipase D2-dependent inh ...... a by cyclic phosphatidic acid.

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J.MOLCEL.2010.07.022

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Phospholipase D2-dependent inh ...... a by cyclic phosphatidic acid.

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Abby L Parrill

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Alyssa Bolen

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Ayako Uchiyama

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Chunxiang Zhang

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Daniel L Baker

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Fabio Re

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Gabor Tigyi

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Guangwei Du

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Huazhang Guo

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Junming Yue

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P2860

Phospholipase D2 localizes to the plasma membrane and regulates angiotensin II receptor endocytosis

Oxidized LDL regulates macrophage gene expression through ligand activation of PPARgamma

PPARgamma promotes monocyte/macrophage differentiation and uptake of oxidized LDL

Phospholipase D2, a distinct phospholipase D isoform with novel regulatory properties that provokes cytoskeletal reorganization

Insulin-induced phospholipase D1 and phospholipase D2 activity in human embryonic kidney-293 cells mediated by the phospholipase C gamma and protein kinase C alpha signalling cascade

Identification of a physiologically relevant endogenous ligand for PPARalpha in liver

A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION

Asymmetry in the PPARgamma/RXRalpha crystal structure reveals the molecular basis of heterodimerization among nuclear receptors

Structural basis for antagonist-mediated recruitment of nuclear co-repressors by PPARalpha

Molecular recognition of nitrated fatty acids by PPARγ

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421-432

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3

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39

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Tamotsu Tsukahara

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2010-08-01T00:00:00Z

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20705243

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3446787

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