2019
DOI: 10.1016/j.bbalip.2018.12.015
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Arginylation regulates adipogenesis by regulating expression of PPARγ at transcript and protein level

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Cited by 9 publications
(6 citation statements)
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“…A 366.3-kb copy-gain CNV encompassing FGFR2 and ATE1 was identified in a proband also deficient for BBS5 (Table 1). ATE1 is reported to affect adipogenesis and adipocyte function (19). Another 858-kb copy-gain CNV affecting the LIPI gene, which is involved in regulation of fat metabolism (20), was identified in a severely obese proband (Table 2).…”
Section: Variants Of Uncertain Significance: Point Mutations In Obesity Genesmentioning
confidence: 99%
“…A 366.3-kb copy-gain CNV encompassing FGFR2 and ATE1 was identified in a proband also deficient for BBS5 (Table 1). ATE1 is reported to affect adipogenesis and adipocyte function (19). Another 858-kb copy-gain CNV affecting the LIPI gene, which is involved in regulation of fat metabolism (20), was identified in a severely obese proband (Table 2).…”
Section: Variants Of Uncertain Significance: Point Mutations In Obesity Genesmentioning
confidence: 99%
“…Peroxisome proliferator-activated receptors (PPARs) are ligand-activated nuclear hormone receptor superfamily transcription factors, consisting of three members, PPARα, PPARγ and PPARδ. Previous studies showed that PPARγ participates in many biological processes, such as adipogenesis, energy metabolism and cellular proliferation (4,5). PPARγ coactivator-1α (PGC-1α) forms a complex with PPARγ, coactivates multiple transcription factors and coordinately governs transcriptional control of several metabolic processes (6).…”
Section: Introductionmentioning
confidence: 99%
“…PPARγ coactivator-1α (PGC-1α) forms a complex with PPARγ, coactivates multiple transcription factors and coordinately governs transcriptional control of several metabolic processes (6). PPARγ downregulation has been found to be associated with pathogenesis of various CVDs, including HF (4,5). PPARγ activation increases glucose and free fatty acid uptake and glycerol lipid biosynthesis (7)(8)(9).…”
Section: Introductionmentioning
confidence: 99%
“…When confluency of the cells reached approximately 70%, the cells were exposed to different doses of the extract CRACE for 24 h or 48 h; subsequently, and cell survivability was measured by MTT (Sigma M2128) assay following standard procedure [16, 17]. 3T3-L1 cells were differentiated following previously reported method with minor modifications [18, 19]. Briefly, 3T3-L1 cells were seeded (3 X 10 5 cells/well of a 35 mm dish) in maintenance medium and allowed to grow till 100% confluency.…”
Section: Methodsmentioning
confidence: 99%
“…Accumulated intracellular lipid was stained with Oil Red O (ORO) as described before with few modifications [19]. Briefly, cells were stained with 3:2 of 0.3% ORO in isopropanol and water for 5–10 min followed by three 60% isopropanol washes, and three water washes.…”
Section: Methodsmentioning
confidence: 99%