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蛋白酶体激活剂 PA28αβ 和 PA200 在棕色脂肪细胞分化和功能中的作用。

The role of proteasome activators PA28αβ and PA200 in brown adipocyte differentiation and function.

机构信息

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

German Center for Cardiovascular Research, Partner Site Munich Heart Alliance, Ludwig-Maximilians-University Hospital, Munich, Germany.

出版信息

Front Endocrinol (Lausanne). 2023 May 2;14:1176733. doi: 10.3389/fendo.2023.1176733. eCollection 2023.

Abstract

INTRODUCTION

Brown adipocytes produce heat through non shivering thermogenesis (NST). To adapt to temperature cues, they possess a remarkably dynamic metabolism and undergo substantial cellular remodeling. The proteasome plays a central role in proteostasis and adaptive proteasome activity is required for sustained NST. Proteasome activators (PAs) are a class of proteasome regulators but the role of PAs in brown adipocytes is unknown. Here, we studied the roles of PA28α (encoded by ) and PA200 (encoded by ) in brown adipocyte differentiation and function.

METHODS

We measured gene expression in mouse brown adipose tissue. In cultured brown adipocytes, we silenced and/or expression through siRNA transfection. We then assessed impact on the ubiquitin proteasome system, brown adipocyte differentiation and function.

RESULTS

We found that and are expressed in brown adipocytes in vivo and in vitro. Through silencing of Psme1 and/or Psme4 expression in cultured brown adipocytes, we found that loss of PAs did not impair proteasome assembly or activity, and that PAs were not required for proteostasis in this model. Loss of and/or did not impair brown adipocyte development or activation, suggesting that PAs are neither required for brown adipogenesis nor NST.

DISCUSSION

In summary, we found no role for and in brown adipocyte proteostasis, differentiation, or function. These findings contribute to our basic understanding of proteasome biology and the roles of proteasome activators in brown adipocytes.

摘要

简介

棕色脂肪细胞通过非颤抖产热(NST)产生热量。为了适应温度信号,它们具有显著的动态代谢,并经历大量的细胞重塑。蛋白酶体在蛋白质稳态中起着核心作用,适应性蛋白酶体活性是持续 NST 的必需条件。蛋白酶体激活剂(PA)是一类蛋白酶体调节剂,但 PA 在棕色脂肪细胞中的作用尚不清楚。在这里,我们研究了 PA28α(由 编码)和 PA200(由 编码)在棕色脂肪细胞分化和功能中的作用。

方法

我们测量了小鼠棕色脂肪组织中的基因表达。在培养的棕色脂肪细胞中,我们通过 siRNA 转染沉默 和/或 的表达。然后,我们评估了对泛素蛋白酶体系统、棕色脂肪细胞分化和功能的影响。

结果

我们发现 和 在体内和体外的棕色脂肪细胞中表达。通过在培养的棕色脂肪细胞中沉默 Psme1 和/或 Psme4 的表达,我们发现失去 PA 不会损害蛋白酶体的组装或活性,并且在这种模型中,PA 对于蛋白质稳态不是必需的。失去 和/或 并不影响棕色脂肪细胞的发育或激活,这表明 PA 既不是棕色脂肪细胞生成所必需的,也不是非颤抖产热所必需的。

讨论

总之,我们没有发现 和 在棕色脂肪细胞蛋白质稳态、分化或功能中的作用。这些发现有助于我们对蛋白酶体生物学和蛋白酶体激活剂在棕色脂肪细胞中的作用的基本理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6cc9/10187037/6983ab43b5d9/fendo-14-1176733-g001.jpg

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