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饮食限制以组织特异性和胱硫醚 γ-裂解酶依赖的方式改变哺乳动物的蛋白质过硫化物组。

Dietary restriction transforms the mammalian protein persulfidome in a tissue-specific and cystathionine γ-lyase-dependent manner.

机构信息

Department of Cardiovascular and Metabolic Sciences, Cleveland Clinic Lerner Research Institute, Cleveland, OH, USA.

Proteomics and Metabolomics Core Laboratory, Cleveland Clinic Lerner Research Institute, Cleveland, OH, USA.

出版信息

Nat Commun. 2021 Mar 19;12(1):1745. doi: 10.1038/s41467-021-22001-w.

Abstract

Hydrogen sulfide (HS) is a cytoprotective redox-active metabolite that signals through protein persulfidation (R-SSH). Despite the known importance of persulfidation, tissue-specific persulfidome profiles and their associated functions are not well characterized, specifically under conditions and interventions known to modulate HS production. We hypothesize that dietary restriction (DR), which increases lifespan and can boost HS production, expands tissue-specific persulfidomes. Here, we find protein persulfidation enriched in liver, kidney, muscle, and brain but decreased in heart of young and aged male mice under two forms of DR, with DR promoting persulfidation in numerous metabolic and aging-related pathways. Mice lacking cystathionine γ-lyase (CGL) have overall decreased tissue protein persulfidation numbers and fail to functionally augment persulfidomes in response to DR, predominantly in kidney, muscle, and brain. Here, we define tissue- and CGL-dependent persulfidomes and how diet transforms their makeup, underscoring the breadth for DR and HS to impact biological processes and organismal health.

摘要

硫化氢(HS)是一种具有细胞保护作用的氧化还原活性代谢物,通过蛋白质过硫化(R-SSH)信号转导。尽管过硫化作用的重要性已被广泛认识,但组织特异性过硫化组谱及其相关功能尚未得到很好的描述,特别是在已知调节 HS 产生的条件和干预下。我们假设,饮食限制(DR)可以增加寿命并促进 HS 的产生,从而扩大组织特异性过硫化组谱。在这里,我们发现年轻和老年雄性小鼠在两种形式的 DR 下,肝脏、肾脏、肌肉和大脑中的蛋白质过硫化作用丰富,但心脏中的过硫化作用减少,DR 促进了许多代谢和衰老相关途径中的过硫化作用。缺乏胱硫醚γ-裂解酶(CGL)的小鼠组织蛋白过硫化数量总体减少,并且无法响应 DR 功能性地增加过硫化组谱,主要是在肾脏、肌肉和大脑中。在这里,我们定义了组织和 CGL 依赖性的过硫化组谱,以及饮食如何改变它们的组成,强调了 DR 和 HS 对生物过程和机体健康的广泛影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f74/7979915/3bf7df009acd/41467_2021_22001_Fig1_HTML.jpg

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