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TLR4 and Insulin Resistance.TLR4 与胰岛素抵抗。
Gastroenterol Res Pract. 2010;2010. doi: 10.1155/2010/212563. Epub 2010 Aug 10.
2
IL-6 and high glucose synergistically upregulate MMP-1 expression by U937 mononuclear phagocytes via ERK1/2 and JNK pathways and c-Jun.白细胞介素-6 和高糖通过 ERK1/2 和 JNK 通路及 c-Jun 协同上调 U937 单核吞噬细胞基质金属蛋白酶-1 的表达。
J Cell Biochem. 2010 May;110(1):248-59. doi: 10.1002/jcb.22532.
3
Adipocyte-mononuclear cell interaction, Toll-like receptor 4 activation, and high glucose synergistically up-regulate osteopontin expression via an interleukin 6-mediated mechanism.脂肪细胞-单核细胞相互作用、Toll 样受体 4 激活和高糖通过白细胞介素 6 介导的机制协同上调骨桥蛋白表达。
J Biol Chem. 2010 Feb 5;285(6):3916-3927. doi: 10.1074/jbc.M109.033951. Epub 2009 Dec 10.
4
TIMPs and cardiac remodeling: 'Embracing the MMP-independent-side of the family'.TIMPs 与心脏重构:“拥抱 MMP 家族的非依赖性一面”。
J Mol Cell Cardiol. 2010 Mar;48(3):445-53. doi: 10.1016/j.yjmcc.2009.09.013. Epub 2009 Sep 30.
5
Mechanisms of obesity and related pathologies: transcriptional control of adipose tissue development.肥胖及相关病理的机制:脂肪组织发育的转录调控
FEBS J. 2009 Oct;276(20):5729-37. doi: 10.1111/j.1742-4658.2009.07302.x. Epub 2009 Sep 15.
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Angiogenesis and development of adipose tissue.血管生成与脂肪组织发育。
Mol Cell Endocrinol. 2010 Apr 29;318(1-2):2-9. doi: 10.1016/j.mce.2009.08.006. Epub 2009 Aug 15.
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Activation of NF-kappaB by palmitate in endothelial cells: a key role for NADPH oxidase-derived superoxide in response to TLR4 activation.棕榈酸酯在内皮细胞中激活核因子κB:NADPH氧化酶衍生的超氧化物在响应Toll样受体4激活中的关键作用。
Arterioscler Thromb Vasc Biol. 2009 Sep;29(9):1370-5. doi: 10.1161/ATVBAHA.109.188813. Epub 2009 Jun 18.
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Saturated fatty acids produce an inflammatory response predominantly through the activation of TLR4 signaling in hypothalamus: implications for the pathogenesis of obesity.饱和脂肪酸主要通过激活下丘脑的TLR4信号传导产生炎症反应:对肥胖发病机制的影响。
J Neurosci. 2009 Jan 14;29(2):359-70. doi: 10.1523/JNEUROSCI.2760-08.2009.
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Adipose tissue macrophages, low grade inflammation and insulin resistance in human obesity.人体肥胖中的脂肪组织巨噬细胞、低度炎症与胰岛素抵抗
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Tlr-4 deficiency selectively protects against obesity induced by diets high in saturated fat.Tlr-4基因缺陷可选择性地预防由高饱和脂肪饮食诱导的肥胖。
Obesity (Silver Spring). 2008 Jun;16(6):1248-55. doi: 10.1038/oby.2008.210. Epub 2008 Apr 10.

TLR4 的激活以及脂肪细胞和单核细胞之间的 IL-6 介导的串扰协同刺激 MMP-1 的表达。

TLR4 activation and IL-6-mediated cross talk between adipocytes and mononuclear cells synergistically stimulate MMP-1 expression.

机构信息

Ralph H. Johnson Veterans Affairs Medical Center, and Division of Endocrinology, Diabetes, and Medical Genetics, Department of Medicine, Medical University of South Carolina, 114 Doughty Street, Charleston, South Carolina 29403, USA.

出版信息

Endocrinology. 2011 Dec;152(12):4662-71. doi: 10.1210/en.2011-1026. Epub 2011 Sep 27.

DOI:10.1210/en.2011-1026
PMID:21952248
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3230059/
Abstract

Obesity is associated with increased monocyte infiltration into adipose tissue and hence increased interaction between adipocytes and monocytes. Although it has been shown that matrix metalloproteinases (MMP) play a critical role in adipose tissue development, the effect of adipocyte and monocyte interaction on MMP production remains largely unknown. Furthermore, although it has been shown that Toll-like receptor 4 (TLR4), a receptor mediating innate immune response, plays an important role in the obesity-associated inflammation and insulin resistance, the effect of TLR4 activation in coculture of adipocytes and monocytes on MMP production has not been investigated. In this study, we cocultured adipocytes with U937 mononuclear cells in a Transwell coculture system and activated TLR4 with lipopolysaccharide or palmitic acid. We found that TLR4 activation and the coculture had a synergistic effect on MMP-1 production. In our further investigation on the underlying mechanisms, it was indicated that adipocyte-derived IL-6 and TLR4 activation acted in concert to synergistically stimulate MMP-1 expression by U937 cells. Taken together, this study has uncovered a novel mechanism potentially involved in MMP-1 up-regulation in adipose tissue, which may facilitate adipose tissue development and obesity.

摘要

肥胖与单核细胞浸润脂肪组织有关,因此脂肪细胞与单核细胞之间的相互作用增加。尽管已经表明基质金属蛋白酶(MMP)在脂肪组织发育中起关键作用,但脂肪细胞和单核细胞相互作用对 MMP 产生的影响在很大程度上仍不清楚。此外,尽管已经表明 Toll 样受体 4(TLR4)作为一种介导先天免疫反应的受体,在肥胖相关炎症和胰岛素抵抗中发挥重要作用,但 TLR4 激活在脂肪细胞和单核细胞共培养物中对 MMP 产生的影响尚未得到研究。在这项研究中,我们在 Transwell 共培养系统中培养脂肪细胞和 U937 单核细胞,并使用脂多糖或棕榈酸激活 TLR4。我们发现 TLR4 激活和共培养对 MMP-1 产生具有协同作用。在我们对潜在机制的进一步研究中,表明脂肪细胞来源的 IL-6 和 TLR4 激活协同作用,协同刺激 U937 细胞的 MMP-1 表达。总之,这项研究揭示了一种潜在参与 MMP-1 在脂肪组织中上调的新机制,这可能有助于脂肪组织发育和肥胖。