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细胞外蛋白酶体的生物学

Biology of the Extracellular Proteasome.

机构信息

Department of Biomolecular Sciences, Weizmann Institute of Science, Rehovot 7610001, Israel.

出版信息

Biomolecules. 2022 Apr 21;12(5):619. doi: 10.3390/biom12050619.

DOI:10.3390/biom12050619
PMID:35625547
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9139032/
Abstract

Proteasomes are traditionally considered intracellular complexes that play a critical role in maintaining proteostasis by degrading short-lived regulatory proteins and removing damaged proteins. Remarkably, in addition to these well-studied intracellular roles, accumulating data indicate that proteasomes are also present in extracellular body fluids. Not much is known about the origin, biological role, mode(s) of regulation or mechanisms of extracellular transport of these complexes. Nevertheless, emerging evidence indicates that the presence of proteasomes in the extracellular milieu is not a random phenomenon, but rather a regulated, coordinated physiological process. In this review, we provide an overview of the current understanding of extracellular proteasomes. To this end, we examine 143 proteomic datasets, leading us to the realization that 20S proteasome subunits are present in at least 25 different body fluids. Our analysis also indicates that while 19S subunits exist in some of those fluids, the dominant proteasome activator in these compartments is the PA28α/β complex. We also elaborate on the positive correlations that have been identified in plasma and extracellular vesicles, between 20S proteasome and activity levels to disease severity and treatment efficacy, suggesting the involvement of this understudied complex in pathophysiology. In addition, we address the considerations and practical experimental methods that should be taken when investigating extracellular proteasomes. Overall, we hope this review will stimulate new opportunities for investigation and thoughtful discussions on this exciting topic that will contribute to the maturation of the field.

摘要

蛋白酶体传统上被认为是细胞内的复合物,通过降解短寿命的调节蛋白和清除受损蛋白,在维持蛋白质稳态方面发挥着关键作用。值得注意的是,除了这些研究充分的细胞内作用外,越来越多的证据表明,蛋白酶体也存在于细胞外体液中。对于这些复合物的起源、生物学作用、调节方式或细胞外运输机制,人们知之甚少。然而,新出现的证据表明,蛋白酶体在细胞外环境中的存在不是一种随机现象,而是一种受调控的、协调的生理过程。在这篇综述中,我们提供了对细胞外蛋白酶体的当前理解的概述。为此,我们检查了 143 个蛋白质组数据集,使我们认识到 20S 蛋白酶体亚基存在于至少 25 种不同的体液中。我们的分析还表明,虽然 19S 亚基存在于其中一些体液中,但这些隔室中主要的蛋白酶体激活剂是 PA28α/β 复合物。我们还详细阐述了在血浆和细胞外囊泡中已经确定的 20S 蛋白酶体与活性水平与疾病严重程度和治疗效果之间的正相关关系,这表明这个研究不足的复合物参与了病理生理学。此外,我们还讨论了在研究细胞外蛋白酶体时应考虑的因素和实际的实验方法。总的来说,我们希望这篇综述将为这一令人兴奋的课题的研究提供新的机会,并引发深入的讨论,从而促进该领域的成熟。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eee3/9139032/fa29f5231db8/biomolecules-12-00619-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eee3/9139032/c23dc00d6748/biomolecules-12-00619-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eee3/9139032/8e6d56505803/biomolecules-12-00619-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eee3/9139032/39073459f3b3/biomolecules-12-00619-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eee3/9139032/fa29f5231db8/biomolecules-12-00619-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eee3/9139032/c23dc00d6748/biomolecules-12-00619-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eee3/9139032/8e6d56505803/biomolecules-12-00619-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eee3/9139032/39073459f3b3/biomolecules-12-00619-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eee3/9139032/fa29f5231db8/biomolecules-12-00619-g004.jpg

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