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撤稿:血小板存储损伤:当前蛋白质组学方法。

Retracted: Platelet storage lesion: current proteomics approach.

机构信息

Department of Transfusion Medicine and Blood Bank, Chhatrapati Shahuji Maharaj Medical University, Lucknow, Uttar Pradesh, India.

出版信息

Platelets. 2011 Feb 22. doi: 10.3109/09537104.2010.547958.

Abstract

The platelet storage lesion (PSL) is best defined as the sum of all deleterious changes leading to progressive damage in platelet structure and function that arise from the time blood is drawn from a donor to the time platelets are transfused to a recipient. Proteomics, the analysis of all proteins of a system at a defined state, has gained increasing interest in hematology as a diagnostic tool. The application of proteomics in transfusion medicine holds promise to revolutionize quality assessment and therapeutic monitoring. The potential of proteomics as a viable tool for the identification of the PSL has since increased dramatically with the development of mass spectrometry and has required the development of quantitative proteomic techniques such as differential gel electrophoresis, isotope-coded affinity tagging, and isotope tagging for relative and absolute quantitation. In principle, two main areas in the field of proteomics have been developed, each of them having its pros and cons. These fields are "profiling" and "functional" proteomics. With the recent implementation of pathogen reduction technologies (PRT) a new dimension of challenges has appeared on the horizon. The treatment of platelet concentrates with either UV-A and a photo sensitizer or UV-C revealed acceleration of PSL development. In conclusion, proteomics thus provides an excellent tool to decode complex processes by identifying novel platelet-expressed proteins and analysing functional changes of the platelet proteome. These recent results suggest that protein kinases might represent one important group of proteins involved in the development of PSL and provide a potential target for inhibition in order to reduce development of PSL. Bacterial risk receives and deserves a lot of attention when it comes to extension of platelet storage; however, determining the quality of platelets during storage needs to be treated with equal importance. As a platelet's life span is 7-10 days, extension of the platelet's shelf life by 2-3 days would improve platelet inventory and efforts of donor recruitment tremendously, as well as to the overall cost of provision of this blood product to patients.

摘要

血小板储存损伤(PSL)最好被定义为从捐献者采血到输注给受者的时间内,导致血小板结构和功能进行性损伤的所有有害变化的总和。蛋白质组学,即分析特定状态下系统的所有蛋白质,作为一种诊断工具,在血液学中越来越受到关注。蛋白质组学在输血医学中的应用有望彻底改变质量评估和治疗监测。随着质谱技术的发展,以及需要开发定量蛋白质组学技术,如差异凝胶电泳、同位素编码亲和标记和相对和绝对定量的同位素标记,蛋白质组学作为识别 PSL 的可行工具的潜力已大大增加。原则上,蛋白质组学领域已经发展出两个主要领域,每个领域都有其优缺点。这些领域是“分析”和“功能”蛋白质组学。随着最近实施病原体减少技术(PRT),新的挑战出现了。用紫外线-A 和光敏剂或紫外线-C 处理血小板浓缩物会加速 PSL 的发展。总之,蛋白质组学通过识别新的血小板表达蛋白和分析血小板蛋白质组的功能变化,为解码复杂过程提供了极好的工具。这些最新结果表明,蛋白激酶可能代表参与 PSL 发展的一个重要蛋白质组,并为抑制 PSL 发展提供了一个潜在的靶点。在延长血小板储存时间方面,细菌风险受到了很多关注;然而,在储存期间确定血小板的质量也需要同等重视。由于血小板的寿命为 7-10 天,将血小板的货架寿命延长 2-3 天将极大地改善血小板库存和献血者招募工作,以及为患者提供这种血液产品的总体成本。

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