"Sticki-ER": Functions of the Platelet Endoplasmic Reticulum.

IF 5.9 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Antioxidants & redox signaling Pub Date : 2024-10-01 Epub Date: 2024-03-27 DOI:10.1089/ars.2024.0566
Yvonne X Kong, Joyce Chiu, Freda H Passam
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引用次数: 0

Abstract

Significance: The primary role of platelets is to generate a thrombus by platelet activation. Platelet activation relies on calcium mobilization from the endoplasmic reticulum (ER). ER resident proteins, which are externalized upon platelet activation, are essential for the function of platelet surface receptors and intercellular interactions. Recent Advances: The platelet ER is a conduit for changes in cellular function in response to the extracellular milieu. ER homeostasis is maintained by an appropriate redox balance, regulated calcium stores and normal protein folding. Alterations in ER function and ER stress results in ER proteins externalizing to the cell surface, including members of the protein disulfide isomerase family (PDIs) and chaperones. Critical Issues: The platelet ER is central to platelet function, but our understanding of its regulation is incomplete. Previous studies have focused on the function of PDIs in the extracellular space, and much less on their intracellular role. How platelets maintain ER homeostasis and how they direct ER chaperone proteins to facilitate intercellular signalling is unknown. Future Directions: An understanding of ER functions in the platelet is essential as these may determine critical platelet activities such as secretion and adhesion. Studies are necessary to understand the redox reactions of PDIs in the intracellular versus extracellular space, as these differentially affect platelet function. An unresolved question is how platelet ER proteins control calcium release. Regulation of protein folding in the platelet and downstream pathways of ER stress require further evaluation. Targeting the platelet ER may have therapeutic application in metabolic and neoplastic disease.

"Sticki-ER":血小板内质网的功能。
重要意义:血小板是血液循环中最小的细胞(直径为 2 微米)。血小板活化是血栓形成的必要条件,它依赖于内质网(ER)的钙动员。血小板活化导致ER驻留蛋白被调动到血小板表面;这些蛋白对血小板受体的功能和细胞间相互作用至关重要:适当的氧化还原平衡、受调节的钙储存和正常的蛋白质折叠可维持ER的平衡。血小板ER平衡被破坏会导致ER应激,从而导致血小板活化。ER应激导致ER蛋白外排到细胞表面,包括蛋白二硫异构酶家族成员和伴侣蛋白:ER是血小板功能的核心,但我们对其调控的了解并不全面。以往的研究侧重于血小板蛋白二硫异构酶家族成员在细胞外空间的功能,而对其在细胞内的作用研究较少。血小板如何维持ER平衡以及如何引导ER伴侣蛋白促进细胞间信号传导尚不清楚:了解ER在血小板中的功能至关重要,因为这些功能可能决定血小板的关键活动,如分泌和粘附。有必要开展研究,以了解血小板二硫异构酶在细胞内和细胞外空间的氧化还原反应,因为这些反应会对血小板功能产生不同影响。尚未解决的问题是血小板ER蛋白如何控制钙释放和蛋白质折叠以应对ER压力。以血小板ER为靶点可能对代谢性和肿瘤性疾病有治疗作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Antioxidants & redox signaling
Antioxidants & redox signaling 生物-内分泌学与代谢
CiteScore
14.10
自引率
1.50%
发文量
170
审稿时长
3-6 weeks
期刊介绍: Antioxidants & Redox Signaling (ARS) is the leading peer-reviewed journal dedicated to understanding the vital impact of oxygen and oxidation-reduction (redox) processes on human health and disease. The Journal explores key issues in genetic, pharmaceutical, and nutritional redox-based therapeutics. Cutting-edge research focuses on structural biology, stem cells, regenerative medicine, epigenetics, imaging, clinical outcomes, and preventive and therapeutic nutrition, among other areas. ARS has expanded to create two unique foci within one journal: ARS Discoveries and ARS Therapeutics. ARS Discoveries (24 issues) publishes the highest-caliber breakthroughs in basic and applied research. ARS Therapeutics (12 issues) is the first publication of its kind that will help enhance the entire field of redox biology by showcasing the potential of redox sciences to change health outcomes. ARS coverage includes: -ROS/RNS as messengers -Gaseous signal transducers -Hypoxia and tissue oxygenation -microRNA -Prokaryotic systems -Lessons from plant biology
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