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E3 ubiquitin ligase DTX4 is required for adipogenic differentiation in 3T3-L1 preadipocytes cell line

机译:e3泛素连接酶DTX4是3T3-L1前脂肪细胞细胞系中的脂肪生成分化所必需的

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Abstract Deltex4 (DTX4) is a member of the Deltex family of proteins. To date several lines of evidences suggest that Deltex family of proteins is closely linked to cell development and cell differentiation. However, little is known about the role of DTX4 in adipogenic differentiation. In this study, we assessed the impact of DTX4 on adipogenic differentiation in?vitro, we found that DTX4 protein expression gradually increased during adipogenic differentiation of 3T3-L1 preadipocytes cell line. While DTX4 stable knockdown by recombinant shRNA lentivirus (sh-DTX4) notably reduced the number of lipid droplets and down-regulated the expression of adipogenic transcription factors C/EBPα and PPARγ and adipogenic markers gene FABP4 and Adipsin. Besides, cell numbers and incorporation of 5-Ethynyl-2′-deoxyuridine (EdU) into cells were significantly decreased during mitotic clonal expansion (MCE) in sh-DTX4 cells postinduction. Furthermore, compared to recombinant shRNA lentivirus control group (sh-CON), the mRNA levels of Wnt signaling genes such as Wnt6, Wnt10b and β-catenin, were obviously elevated in sh-DTX4 group at day 3 of postinduction. Taken together, our results indicate that DTX4 stable knockdown inhibits adipogenesis of 3T3-L1 cells through inhibiting C/EBPα and PPARγ, arresting mitotic clonal expansion and regulating Wnt signaling pathway. Highlights ? DTX4 protein expression gradually increased during adipogenic differentiation in 3T3-L1 cells. ? Stable knockdown of DTX4 inhibits adipogenic differentiation. ? Stable knockdown of DTX4 impairs mitotic clonal expansion, elevates expression levels of WNT signaling genes. ]]>
机译:摘要Deltex4(DTX4)是蛋白质蛋白质的德国家族的成员。迄今为止,几条证据表明,德国蛋白质系列与细胞发育和细胞分化密切相关。然而,关于DTX4在脂肪生成分化中的作用很少。在这项研究中,我们评估了DTX4对体外脂肪异化分化的影响,我们发现DTX4蛋白表达在3T3-L1前脂肪细胞细胞系的脂肪生成分化期间逐渐增加。虽然DTX4通过重组shRNA慢病毒(SH-DTX4)稳定的敲低(SH-DTX4)显着降低了脂质液滴的数量,下调脂肪转录因子C /EBPα和PPARγ和脂肪生成标记物基因FABP4和Adipsin的表达。此外,在SH-DTX4细胞后的有丝分裂克隆膨胀(MCE)期间,细胞数和将5-乙炔基-2'-脱氧尿苷(EDU)掺入细胞中显着降低。此外,与重组ShRNA慢病毒对照组(SH-CON)相比,在PostInuction第3天的SH-DTX4组中,Wnt信号传导基因如Wnt6,Wnt10b和β-catenin的MRNA水平明显升高。我们的结果表明,DTX4稳定敲低通过抑制C /EBPα和PPARγ,抑制有丝分裂克隆膨胀和调节Wnt信号传导途径来抑制3T3-L1细胞的脂肪生成。强调 ? DTX4蛋白表达在3T3-L1细胞中的脂肪生成分化期间逐渐增加。还DTX4的稳定敲低抑制脂肪生成分化。还DTX4稳定敲低损害有丝分裂克隆膨胀,提升了WNT信号传导基因的表达水平。 ]]>

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