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泛素在棕色脂肪细胞蛋白稳态和产热中的作用。

Role of Ubiquilins for Brown Adipocyte Proteostasis and Thermogenesis.

机构信息

Institute for Cardiovascular Prevention (IPEK), Ludwig-Maximilians-University, Munich, Germany.

German Center for Cardiovascular Research, Partner Site Munich Heart Alliance, Technische Universität München, Munich, Germany.

出版信息

Front Endocrinol (Lausanne). 2021 Sep 28;12:739021. doi: 10.3389/fendo.2021.739021. eCollection 2021.

DOI:10.3389/fendo.2021.739021
PMID:34650520
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8505974/
Abstract

The acclimatization of brown adipose tissue (BAT) to sustained cold exposure requires an adaptive increase in proteasomal protein quality control. Ubiquilins represent a recently identified family of shuttle proteins with versatile functions in protein degradation, such as facilitating substrate targeting and proteasomal degradation. However, whether ubiquilins participate in brown adipocyte function has not been investigated so far. Here, we determine the role of ubiquilins for proteostasis and non-shivering thermogenesis in brown adipocytes. We found that and are highly expressed in BAT and their expression was induced by cold and proteasomal inhibition. Surprisingly, silencing of ubiquilin gene expression (one or multiple in combinations) did not lead to aggravated ER stress or inflammation. Moreover, ubiquitin level and proteasomal activity under basal conditions were not impacted by loss of ubiquilins. Also, non-shivering thermogenesis measured by norepinephrine-induced respiration remained intact after loss of ubiquilins. In conclusion, ubiquilin proteins are highly abundant in BAT and regulated by cold, but they are dispensable for brown adipocyte proteostasis and thermogenesis.

摘要

棕色脂肪组织 (BAT) 对持续寒冷暴露的适应需要蛋白酶体蛋白质量控制的适应性增加。泛素是一类最近被发现的穿梭蛋白家族,在蛋白质降解中具有多种功能,例如促进底物靶向和蛋白酶体降解。然而,泛素是否参与棕色脂肪细胞的功能迄今尚未得到研究。在这里,我们确定了泛素在棕色脂肪细胞中的蛋白稳态和非颤抖性产热中的作用。我们发现 和 在 BAT 中高度表达,其表达受寒冷和蛋白酶体抑制诱导。令人惊讶的是,泛素基因表达(一种或多种组合)的沉默并没有导致内质网应激或炎症加重。此外,基础条件下泛素水平和蛋白酶体活性不受泛素缺失的影响。此外,去甲肾上腺素诱导的呼吸所测量的非颤抖性产热在泛素缺失后仍然完整。总之,泛素蛋白在 BAT 中含量丰富,受寒冷调节,但它们对于棕色脂肪细胞的蛋白稳态和产热是可有可无的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/226f/8505974/6f4f55060898/fendo-12-739021-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/226f/8505974/973985fdccbc/fendo-12-739021-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/226f/8505974/05c92bc087c4/fendo-12-739021-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/226f/8505974/5353513ae18e/fendo-12-739021-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/226f/8505974/6f4f55060898/fendo-12-739021-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/226f/8505974/973985fdccbc/fendo-12-739021-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/226f/8505974/05c92bc087c4/fendo-12-739021-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/226f/8505974/5353513ae18e/fendo-12-739021-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/226f/8505974/6f4f55060898/fendo-12-739021-g004.jpg

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本文引用的文献

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Structure, dynamics and functions of UBQLNs: at the crossroads of protein quality control machinery.UBQLNs 的结构、动态和功能:处于蛋白质质量控制机制的十字路口。
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Amyotrophic lateral sclerosis-linked UBQLN2 mutants inhibit endoplasmic reticulum to Golgi transport, leading to Golgi fragmentation and ER stress.肌萎缩侧索硬化相关 UBQLN2 突变体抑制内质网到高尔基体的运输,导致高尔基体碎片化和内质网应激。
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