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在黄鼠脂肪组织从冬眠中苏醒的过程中,促炎性晚期糖基化终末产物受体(AGE-RAGE)信号通路被激活。

Pro-inflammatory AGE-RAGE signaling is activated during arousal from hibernation in ground squirrel adipose.

作者信息

Logan Samantha M, Storey Kenneth B

机构信息

Institute of Biochemistry, Departments of Biology and Chemistry, Carleton University, Ottawa, Ontario, Canada.

出版信息

PeerJ. 2018 Jun 4;6:e4911. doi: 10.7717/peerj.4911. eCollection 2018.

Abstract

BACKGROUND

Inflammation is generally suppressed during hibernation, but select tissues (e.g. lung) have been shown to activate both antioxidant and pro-inflammatory pathways, particularly during arousal from torpor when breathing rates increase and oxidative metabolism fueling the rewarming process produces more reactive oxygen species. Brown and white adipose tissues are now understood to be major hubs for the regulation of immune and inflammatory responses, yet how these potentially damaging processes are regulated by fat tissues during hibernation has hardly been studied. The advanced glycation end-product receptor (RAGE) can induce pro-inflammatory responses when bound by AGEs (which are glycated and oxidized proteins, lipids, or nucleic acids) or damage associated molecular pattern molecules (DAMPs, which are released from dying cells).

METHODS

Since gene expression and protein synthesis are largely suppressed during torpor, increases in AGE-RAGE pathway proteins relative to a euthermic control could suggest some role for these pro-inflammatory mediators during hibernation. This study determined how the pro-inflammatory AGE-RAGE signaling pathway is regulated at six major time points of the torpor-arousal cycle in brown and white adipose from a model hibernator, . Immunoblotting, RT-qPCR, and a competitive ELISA were used to assess the relative gene expression and protein levels of key regulators of the AGE-RAGE pathway during a hibernation bout.

RESULTS

The results of this study revealed that RAGE is upregulated as animals arouse from torpor in both types of fat, but AGE and DAMP levels either remain unchanged or decrease. Downstream of the AGE-RAGE cascade, was more highly expressed during arousal in brown adipose.

DISCUSSION

An increase in RAGE protein levels and elevated mRNA levels of the downstream transcription factor during arousal suggest the pro-inflammatory response is upregulated in adipose tissue of the hibernating ground squirrel. It is unlikely that this cascade is activated by AGEs or DAMPs. This research sheds light on how a fat-but-fit organism with highly regulated metabolism may control the pro-inflammatory AGE-RAGE pathway, a signaling cascade that is often dysregulated in other obese organisms.

摘要

背景

在冬眠期间,炎症通常受到抑制,但特定组织(如肺)已被证明会激活抗氧化和促炎途径,尤其是在从蛰伏状态苏醒期间,此时呼吸频率增加,为复温过程提供能量的氧化代谢会产生更多活性氧。现在已知棕色和白色脂肪组织是免疫和炎症反应调节的主要枢纽,但在冬眠期间这些潜在的破坏性过程如何由脂肪组织调节几乎尚未得到研究。晚期糖基化终产物受体(RAGE)在与晚期糖基化终产物(AGEs,即糖基化和氧化的蛋白质、脂质或核酸)或损伤相关分子模式分子(DAMPs,从垂死细胞释放)结合时可诱导促炎反应。

方法

由于在蛰伏期间基因表达和蛋白质合成在很大程度上受到抑制,相对于正常体温对照,AGE-RAGE途径蛋白的增加可能表明这些促炎介质在冬眠期间发挥了某种作用。本研究确定了在一种冬眠动物的棕色和白色脂肪的蛰伏-苏醒周期的六个主要时间点,促炎的AGE-RAGE信号通路是如何被调节的。在一次冬眠期间,使用免疫印迹、RT-qPCR和竞争性ELISA来评估AGE-RAGE途径关键调节因子的相对基因表达和蛋白质水平。

结果

本研究结果表明,在两种类型的脂肪中,随着动物从蛰伏状态苏醒,RAGE上调,但AGE和DAMP水平要么保持不变,要么下降。在AGE-RAGE级联反应的下游,在棕色脂肪苏醒期间表达更高。

讨论

苏醒期间RAGE蛋白水平的增加以及下游转录因子mRNA水平的升高表明,冬眠地松鼠的脂肪组织中促炎反应上调。该级联反应不太可能由AGEs或DAMPs激活。这项研究揭示了一种代谢高度调节的肥胖但健康的生物体如何控制促炎的AGE-RAGE途径——这是一种在其他肥胖生物体中经常失调的信号级联反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9642/5991297/229687848bbf/peerj-06-4911-g001.jpg

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