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维甲酸通过调节C/EBPβ磷酸化和下调Srebf1a表达来抑制脂肪生成。

Retinoic Acid Inhibits Adipogenesis Modulating C/EBPβ Phosphorylation and Down Regulating Srebf1a Expression.

作者信息

Ayala-Sumuano Jorge-Tonatiuh, Vélez-DelValle Cristina, Marsch-Moreno Meytha, Beltrán-Langarica Alicia, Hernández-Mosqueira Claudia, Kuri-Harcuch Walid

机构信息

Instituto de Neurobiología, Universidad Nacional Autónoma de México, Blvd, Juriquilla 3001, Juriquilla, Querétaro, Mexico.

Department of Cell Biology, Centro de Investigación y de Estudios Avanzados del IPN, Avenida Instituto Politécnico Nacional 2508, San Pedro Zacatenco, Mexico City, Mexico.

出版信息

J Cell Biochem. 2016 Mar;117(3):629-37. doi: 10.1002/jcb.25311. Epub 2015 Sep 29.

Abstract

Adipogenesis comprises a complex network of signaling pathways and transcriptional cascades; the GSK3β-C/EBPβ-srebf1a axis is a critical signaling pathway at early stages leading to the expression of PPARγ2, the master regulator of adipose differentiation. Previous work has demonstrated that retinoic acid inhibits adipogenesis affecting different signaling pathways. Here, we evaluated the anti-adipogenic effect of retinoic acid on the adipogenic transcriptional cascade, and the expression of adipogenic genes cebpb, srebf1a, srebf1c, pparg2, and cebpa. Our results demonstrate that retinoic acid blocks adipose differentiation during commitment, returning cells to an apparent non-committed state, since they have to be newly induced to adipose conversion after the retinoid is removed from the culture medium. Retinoic acid down regulates the expression of the adipogenic genes, srebf1a, srebf1c, pparg2, and cebpa; however, it did not down regulate the expression of cebpb, but it inhibited C/EBPβ phosphorylation at Thr188, a critical step for the progression of the adipogenic program. We also found that RA inhibition of adipogenesis did not increase the expression of dlk1, the gene encoding for Pref1, a well-known anti-adipogenic factor.

摘要

脂肪生成包括一个由信号通路和转录级联反应组成的复杂网络;糖原合成酶激酶3β(GSK3β)-C/EBPβ-固醇调节元件结合转录因子1a(srebf1a)轴是早期导致脂肪分化主要调节因子PPARγ2表达的关键信号通路。先前的研究表明,视黄酸通过影响不同的信号通路来抑制脂肪生成。在此,我们评估了视黄酸对脂肪生成转录级联反应以及脂肪生成相关基因cebpb、srebf1a、srebf1c、pparg2和cebpa表达的抗脂肪生成作用。我们的结果表明,视黄酸在细胞定向分化过程中阻断脂肪分化,使细胞回到明显未定向的状态,因为在从培养基中去除类视黄醇后,它们必须重新被诱导进行脂肪转化。视黄酸下调脂肪生成相关基因srebf1a、srebf1c、pparg2和cebpa的表达;然而,它并未下调cebpb的表达,但抑制了C/EBPβ在苏氨酸188位点的磷酸化,这是脂肪生成程序进展的关键步骤。我们还发现,视黄酸对脂肪生成的抑制并未增加dlk1的表达,dlk1是编码Pref1的基因,Pref1是一种著名的抗脂肪生成因子。

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