Suppr超能文献

肿瘤坏死因子(TNF)α作为地中海金头鲷(Sparus aurata L.)脂肪组织量的调节因子。

Tumour necrosis factor (TNF)alpha as a regulator of fat tissue mass in the Mediterranean gilthead sea bream (Sparus aurata L.).

作者信息

Saera-Vila Alfonso, Calduch-Giner Josep Alvar, Navarro Isabel, Pérez-Sánchez Jaume

机构信息

Instituto de Acuicultura de Torre de la Sal (CSIC), 12595 Ribera de Cabanes, Castellón, Spain.

出版信息

Comp Biochem Physiol B Biochem Mol Biol. 2007 Mar;146(3):338-45. doi: 10.1016/j.cbpb.2006.11.003. Epub 2006 Nov 21.

Abstract

The study was undertaken to analyze the lipolytic effect and transcriptional regulation of tumour necrosis factor (TNF)alpha in gilthead sea bream (Sparus aurata L.). The study was also focused on the transcriptional regulation and analysis of the 5-flanking region of lipoprotein lipase (LPL) in an attempt to identify cis-regulatory elements that would support the TNFalpha-mediated effects. The lipolytic effect of TNFalpha was evidenced by the increased release of glycerol in the culture medium of freshly isolated adipocytes. This observation, in addition to the summer up-regulation of TNFalpha transcripts in liver and mesenteric adipose tissue, supported a key role of TNFalpha as a fish limiting factor of tissue fat mass. Accordingly, TNFalpha expression in liver and mesenteric adipose tissue was reduced by fasting. Furthermore, the up-regulated expression of TNFalpha in the skeletal muscle of older fish can represent an adaptive response to limit the enhanced lipid influx towards muscle. A close positive association between LPL and TNFalpha transcripts supported the contribution of TNFalpha as a part of a regulatory network that exerts an inhibitory tonus upon the expression of LPL, which in turns limits the tissue uptake of fatty acids and the ultimate increase of tissue lipid reservoirs. The precise mechanism for the inhibition of LPL gene expression by TNFalpha remains to be established in fish, but analysis of the 5'-flanking region evidenced the conservation through vertebrate evolution of a functional OCT-1/NF-Y site that would mediate the TNFalpha effects on LPL expression.

摘要

本研究旨在分析肿瘤坏死因子(TNF)α对金头鲷(Sparus aurata L.)的脂解作用及其转录调控。该研究还聚焦于脂蛋白脂肪酶(LPL)5'侧翼区域的转录调控与分析,试图识别能够支持TNFα介导效应的顺式调控元件。新鲜分离的脂肪细胞培养基中甘油释放量增加,证明了TNFα的脂解作用。这一观察结果,连同肝脏和肠系膜脂肪组织中TNFα转录本在夏季的上调,支持了TNFα作为鱼类组织脂肪量限制因子的关键作用。因此,禁食可降低肝脏和肠系膜脂肪组织中TNFα的表达。此外,老年鱼骨骼肌中TNFα表达上调可能是一种适应性反应,以限制脂质向肌肉的大量流入。LPL与TNFα转录本之间紧密的正相关关系支持了TNFα作为调控网络一部分的作用,该网络对LPL的表达施加抑制性张力,进而限制脂肪酸的组织摄取以及组织脂质储备的最终增加。TNFα抑制LPL基因表达的确切机制在鱼类中仍有待确定,但对5'侧翼区域的分析表明,功能性OCT-1/NF-Y位点在脊椎动物进化过程中具有保守性,该位点可介导TNFα对LPL表达的影响。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验