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首页> 外文期刊>Biochimica et biophysica acta. Molecular cell research >Cul3 neddylation is crucial for gradual lipid droplet formation during adipogenesis
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Cul3 neddylation is crucial for gradual lipid droplet formation during adipogenesis

机译:Cul3 Neddylation对于脂肪生成期间的逐渐脂质液滴形成至关重要

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Cullin 3 (Cul3) belongs to the family of cullins (Cul1-7) providing the scaffold for cullin-RING ubiquitin (Ub) ligases (CRLs), which are activated by neddylation and represent essential E3 ligases of the Ub proteasome system. During adipogenic differentiation neddylated Cul3 accumulates in LiSa-2 preadipocytes. Downregulation of Cul3 and inhibition of neddylation by MLN4924 blocks the formation of lipid droplets (LDs), the lipid storage organelles and markers of adipogenesis. Neddylation of Cul3 coincides with an increase of Rab18, a GTPase associated with LDs. Immunoprecipitation and confocal fluorescence microscopy revealed physical association of Cul3 and Rab18 at the membrane of LDs. RhoA, a suppressor of adipogenesis decreased during differentiation. Our results in LiSa-2 cells, but also mouse embryonic fibroblasts revealed a connection between Cul3, Rab18 and RhoA. Downregulation of Cul3 led to a marked increase in RhoA protein expression after 6 days of LiSa-2 cell differentiation, suggesting that Cul3 is involved in the regulation of RhoA stability.
机译:Cullin 3(Cul3)属于提供Cullin-Ring泛素(UB)连接的支架(CUL1-7)的Cullins(CUL1-7),其通过NedDylation激活并代表UB蛋白酶体系的基本E3连接酶。在脂肪生成的分化期间,Neddylated Cul3在Lisa-2前脂肪细胞中累积。 CUL3的下调和MLN4924阻断脂质液滴(LDS),脂质储存机组和脂肪发生标记的形成。 Cul3的Neddylation与Rab18的增加一致,与LD相关的GTP酶。免疫沉淀和共聚焦荧光显微镜显示CUL3和RAB18在LDS膜上的物理缔合。 RhoA,脂肪发生的抑制因子在分化期间降低。我们的结果在LISA-2细胞中,但小鼠胚胎成纤维细胞显示CUL3,RAB18和RHOA之间的连接。 CUL3的下调导致RISA-2细胞分化6天后RHOA蛋白表达的显着增加,表明CUL3参与了RHOA稳定性的调节。

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