Acsl4 degradation
WebApr 14, 2024 · Collectively, these data demonstrated that 20-HETE, a metabolite of AA, enhances ACSL4 degradation by activating the PKC signaling pathway and inducing the expression of E3 ubiquitin ligase FBXO10. WebMay 27, 2024 · Pretreatment of these cells with ferrostatin-1 (Fer-1), an arylalkylamine that was identified as one of the first chemical inhibitors of ferroptosis, which has been suggested to act by preventing oxidative damage to membrane lipids , blocked ACSL4 degradation completely (Fig. 2a). These data validate the integral role of ACSL4 in ferroptosis ...
Acsl4 degradation
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WebArachidonic acid induces ACSL4 protein degradation 1659 ACSL4 mRNA half-life determination g protein were incubated with anti-ACSL4 antibody or a control antibody (rabbit IgG) overnight at... WebIt has been reported that in hepatic cells and primary cortical neurons, ACSL4 is degraded mainly through the proteasome pathway [34,35]. However, as previously hypothesized, the lysosome...
WebFeb 12, 2024 · ACSL4 acyl-CoA synthetase long chain family member 4 Gene ID: 2182, updated on 12-Feb-2024 Gene type: protein coding Also known as: ACS4; FACL4; LACS4; MRX63; MRX68; XLID63 See all available tests in GTR for this gene Go to complete Gene record for ACSL4 Go to Variation Viewer for ACSL4 variants Summary WebMar 21, 2024 · ACSL4 (Acyl-CoA Synthetase Long Chain Family Member 4) is a Protein Coding gene. Diseases associated with ACSL4 include Intellectual Developmental Disorder, X-Linked 63 and Stroke, Ischemic.Among its related pathways are Fatty acid metabolism and Integration of energy metabolism.Gene Ontology (GO) annotations related to this …
WebFACL proteins are important for synthesis of cellular lipids and for β-oxidation degradation. Specifically, ACSL proteins catalyze the activation of long-chain fatty acids to acyl-CoAs, which can be metabolized to form CO2, triacylglycerol (TAG), phospholipids (PL) and cholesteryl esters (CE). WebAug 8, 2024 · The degradation of Nrf2 is mediated by Keap1-dependent ubiquitin-proteasome pathway under quiescent conditions ... ACSL4 forms acyl-CoAs by catalyzing fatty acids and affects the lipid composition . Activation of ACSL4 has been indicated to promote ferroptosis [47, 57].
WebMar 15, 2024 · Hepcidin acts by inducing endocytosis and subsequent degradation of FPN. The Tet1-RNF217-FPN axis, a newly recognized pathway, ... (ACSL4) and lysophosphatidylcholine acyltransferase 3 (LPCAT3) are important enzymes responsible for the biosynthesis and remodeling of PUFA-phosphatidylethanolamines .
WebAug 27, 2024 · As shown in Fig. 2A, the expression of ACSL4 mRNA was reduced >90% in the adrenal (P < 0.001), Leydig cells (P < 0.001), and ovary (P < 0.01) of KO mice … human ab serum gemini bioproductsWebNov 24, 2024 · Peroxisome-dependent and independent initiation of ferroptotic pathways. The peroxidation of PUFAs by ALOXs or POR to produce LOOH is an important step in promoting ferroptosis. The synthesis of ... human \u0026 beingsWebHepatic ACSL4 was significantly decreased in both of our NASH models and is also decreased by high-fat diet feeding in mice (36). Interestingly, free arachidonic acid causes ACSL4 to be... human ab serum hp1022WebMar 19, 2024 · Identification of p115 as a novel ACSL4 interacting protein and its role in regulating ACSL4 degradation. Journal of Proteomics, Volume 229, 2024, Article 103926. Show abstract. Long-chain acyl-CoA synthetase 4 (ACSL4) is an ACSL family member that exhibits unique substrate preference for arachidonic acid. ACSL4 has a functional role in … human ab serum sigma h4522Web图2c-d:acsl4低表达的肺腺癌患者的无进展生存期(pfs)和总生存期(os)更差。 作者对tcga数据库中524例肺腺癌患者进行通路富集分析,值得注意的是,gsea和go富集分析 … human ab serum gemini bioWebOverexpression of ACSL4 results in a higher rate of arachidonoyl-CoA synthesis, increased 20:4 incorporation into phosphatidylethanolamine, phosphatidylinositol, and triacylglycerol, and reduced cellular levels of unesterified 20:4. Additionally, ACSL4 regulates PGE 2 release from human smooth muscle cells. human ab serum vs fbsWebIt has been reported that in hepatic cells and primary cortical neurons, ACSL4 is degraded mainly through the proteasome pathway [34,35]. However, as previously hypothesized, … human abacus