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本文引用的文献

1
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Am J Physiol Endocrinol Metab. 2010 Sep;299(3):E335-40. doi: 10.1152/ajpendo.00243.2010. Epub 2010 Jun 8.
2
Receptor interacting protein 140 regulates expression of uncoupling protein 1 in adipocytes through specific peroxisome proliferator activated receptor isoforms and estrogen-related receptor alpha.受体相互作用蛋白140通过特定的过氧化物酶体增殖物激活受体亚型和雌激素相关受体α调节脂肪细胞中解偶联蛋白1的表达。
Mol Endocrinol. 2007 Jul;21(7):1581-92. doi: 10.1210/me.2007-0103. Epub 2007 Apr 24.
3
Vitamin B6 conjugation to nuclear corepressor RIP140 and its role in gene regulation.维生素B6与核共抑制因子RIP140的结合及其在基因调控中的作用。
Nat Chem Biol. 2007 Mar;3(3):161-5. doi: 10.1038/nchembio861. Epub 2007 Feb 4.
4
Involvement of membrane protein GDE2 in retinoic acid-induced neurite formation in Neuro2A cells.膜蛋白GDE2参与维甲酸诱导Neuro2A细胞的神经突形成。
FEBS Lett. 2007 Feb 20;581(4):712-8. doi: 10.1016/j.febslet.2007.01.035. Epub 2007 Jan 24.
5
Vitamin B6 suppresses NF-kappaB activation in LPS-stimulated mouse macrophages.
Int J Mol Med. 2005 Dec;16(6):1071-5.
6
RIP140-targeted repression of gene expression in adipocytes.脂肪细胞中RIP140靶向的基因表达抑制
Mol Cell Biol. 2005 Nov;25(21):9383-91. doi: 10.1128/MCB.25.21.9383-9391.2005.
7
PPAR-gamma agonists inhibit toll-like receptor-mediated activation of dendritic cells via the MAP kinase and NF-kappaB pathways.过氧化物酶体增殖物激活受体γ激动剂通过丝裂原活化蛋白激酶和核因子κB途径抑制Toll样受体介导的树突状细胞活化。
Blood. 2005 Dec 1;106(12):3888-94. doi: 10.1182/blood-2004-12-4709. Epub 2005 Aug 16.
8
Corepressors selectively control the transcriptional activity of PPARgamma in adipocytes.共抑制因子选择性地控制脂肪细胞中PPARγ的转录活性。
Genes Dev. 2005 Feb 15;19(4):453-61. doi: 10.1101/gad.1263305. Epub 2005 Jan 28.
9
Antineoplastic effects of peroxisome proliferator-activated receptor gamma agonists.过氧化物酶体增殖物激活受体γ激动剂的抗肿瘤作用
Lancet Oncol. 2004 Jul;5(7):419-29. doi: 10.1016/S1470-2045(04)01509-8.
10
Nuclear receptor corepressor RIP140 regulates fat accumulation.核受体共抑制因子RIP140调节脂肪积累。
Proc Natl Acad Sci U S A. 2004 Jun 1;101(22):8437-42. doi: 10.1073/pnas.0401013101. Epub 2004 May 20.

维生素B6调节过氧化物酶体增殖物激活受体γ靶基因的mRNA表达。

Vitamin B6 regulates mRNA expression of peroxisome proliferator-activated receptor-γ target genes.

作者信息

Yanaka Noriyuki, Kanda Mayumi, Toya Keigo, Suehiro Haruna, Kato Norihisa

机构信息

Department of Bioresource Science and Technology, Graduate School of Biosphere Science, Hiroshima University, Higashi-Hiroshima 739-8528, Japan.

出版信息

Exp Ther Med. 2011 May;2(3):419-424. doi: 10.3892/etm.2011.238. Epub 2011 Mar 21.

DOI:10.3892/etm.2011.238
PMID:22977520
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3440721/
Abstract

We previously demonstrated that vitamin B6 suppresses tumorigenesis in the colon of mice and exerts an anti-inflammatory effect through the inhibition of NF-κB activation. As these effects resemble the pharmacological properties of thiazolidinedione (TZD), a synthetic peroxisome proliferator-activated receptor-γ (PPARγ) ligand, this study was designed to examine the effect of vitamin B6 on the activation of PPARγ and adipogenesis in 3T3-L1 adipocyte cells. Pyridoxal 5'-phosphate (PLP), one of the vitamin B6 derivatives, was shown to promote adipogenesis in the 3T3-L1 adipocytes. In addition, PLP specifically induced mRNA expression of PPARγ target genes in the 3T3-L1 adipocytes and enhanced the lipid accumulation and adipocyte fatty acid-binding protein (aP2) mRNA expression in NIH3T3 cells stably expressing PPARγ. Furthermore, the administration of vitamin B6 increased the expression of aP2 mRNA in mouse adipose tissues. Collectively, these observations suggest a novel function of vitamin B6 as an activator for PPARγ, which may contribute to the anti-tumor and anti-inflammatory effects of vitamin B6.

摘要

我们之前证明,维生素B6可抑制小鼠结肠肿瘤发生,并通过抑制核因子κB(NF-κB)激活发挥抗炎作用。由于这些作用类似于噻唑烷二酮(TZD)的药理特性,TZD是一种合成的过氧化物酶体增殖物激活受体γ(PPARγ)配体,本研究旨在检测维生素B6对3T3-L1脂肪细胞中PPARγ激活及脂肪生成的影响。维生素B6衍生物之一的磷酸吡哆醛(PLP)可促进3T3-L1脂肪细胞的脂肪生成。此外,PLP可特异性诱导3T3-L1脂肪细胞中PPARγ靶基因的mRNA表达,并增强稳定表达PPARγ的NIH3T3细胞中的脂质积累及脂肪细胞脂肪酸结合蛋白(aP2)mRNA表达。此外,给予维生素B6可增加小鼠脂肪组织中aP2 mRNA的表达。总体而言,这些观察结果提示维生素B6作为PPARγ激活剂的新功能,这可能有助于维生素B6的抗肿瘤和抗炎作用。