Toward standardization and a concerted vision for platelet proteomics research: communication from the SSC of the ISTH.

IF 5.5 2区 医学 Q1 HEMATOLOGY
Patricia Martínez-Botía, Samuel Tassi Yunga, Paulina Szklanna, Ozgun Babur, Andrew Emili, Phillip A Wilmarth, Johan W M Heemskerk, Patricia B Maguire, Aaron F J Iding, Sofia Ramström, Ángel García, Joseph E Aslan, Laura Gutiérrez
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引用次数: 0

Abstract

Over the past 3 decades, omics technologies have revolutionized our understanding of platelet molecular content and organization, enabling the systematic analyses of platelet physiology. Among these approaches, proteomics has been especially significant in discovering as well as validating molecular mechanisms of platelet function in health and disease. However, several conceptual and practical challenges continue to limit the full utility of platelet proteomics tools and data. Methodological and analytical inconsistencies remain a key concern, with biological and technical variables exerting substantial influence on study outcomes and interpretation. These issues are compounded by the rapid pace of proteomics tool development and dataset collection, outstripping efforts to standardize best practices and ensure consensus, as platelet proteomics consolidates itself as a tool for research even outside the thrombosis and hemostasis field. In this communication from the International Society on Thrombosis and Haemostasis Scientific and Standardization Committee, we highlight recent advances in platelet proteomics studies, and we identify where collective efforts can strengthen experimental design, execution, and analysis. As a practical recommendation, we encourage platelet biologists to recognize current discrepancies and advance efforts to standardize and customize methods and reporting practices, including blood collection, platelet isolation, data acquisition, and data interpretation. By aligning protocols and ensuring detailed reporting, the field can more effectively integrate proteomics findings and accelerate our understanding of platelet biology.

在过去的三十年里,全息技术彻底改变了我们对血小板分子内容和组织的认识,使我们能够对血小板生理学进行系统分析。在这些方法中,蛋白质组学在发现和验证健康与疾病中血小板功能的分子机制方面尤为重要。然而,一些概念和实践上的挑战仍然限制着血小板蛋白质组学工具和数据的充分发挥作用。方法和分析的不一致仍然是一个主要问题,生物和技术变量对研究结果和解释产生了重大影响。随着血小板蛋白质组学逐渐成为血栓与止血领域以外的研究工具,蛋白质组学工具的快速开发和数据集的快速收集使这些问题变得更加复杂。在国际血栓与止血学会(ISTH)科学与标准化委员会(SSC)的这篇通讯中,我们重点介绍了血小板蛋白质组学研究的最新进展,并指出了集体努力可以加强实验设计、执行和分析的地方。作为一项切实可行的建议,我们鼓励血小板生物学家认识到目前存在的差异,并努力推进方法和报告实践的标准化和定制化,包括血液采集、血小板分离、数据采集和数据解读。通过统一方案和确保详细的报告,该领域可以更有效地整合蛋白质组学研究结果,加快我们对血小板生物学的理解。
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来源期刊
Journal of Thrombosis and Haemostasis
Journal of Thrombosis and Haemostasis 医学-外周血管病
CiteScore
24.30
自引率
3.80%
发文量
321
审稿时长
1 months
期刊介绍: The Journal of Thrombosis and Haemostasis (JTH) serves as the official journal of the International Society on Thrombosis and Haemostasis. It is dedicated to advancing science related to thrombosis, bleeding disorders, and vascular biology through the dissemination and exchange of information and ideas within the global research community. Types of Publications: The journal publishes a variety of content, including: Original research reports State-of-the-art reviews Brief reports Case reports Invited commentaries on publications in the Journal Forum articles Correspondence Announcements Scope of Contributions: Editors invite contributions from both fundamental and clinical domains. These include: Basic manuscripts on blood coagulation and fibrinolysis Studies on proteins and reactions related to thrombosis and haemostasis Research on blood platelets and their interactions with other biological systems, such as the vessel wall, blood cells, and invading organisms Clinical manuscripts covering various topics including venous thrombosis, arterial disease, hemophilia, bleeding disorders, and platelet diseases Clinical manuscripts may encompass etiology, diagnostics, prognosis, prevention, and treatment strategies.
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