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血小板分离和核苷酸酶测定:揭示血管系统与免疫系统之间通讯的功能方面。

Platelets isolation and ectonucleotidase assay: Revealing functional aspects of the communication between the vasculature and the immune system.

机构信息

Laboratory of Vascular Biochemistry, Center for Natural and Human Sciences, Federal University of ABC, Santo André, SP, Brazil.

Laboratory of Vascular Biochemistry, Center for Natural and Human Sciences, Federal University of ABC, Santo André, SP, Brazil.

出版信息

J Immunol Methods. 2024 Oct;533:113746. doi: 10.1016/j.jim.2024.113746. Epub 2024 Aug 22.

Abstract

Platelets are enucleated fragments of cells with a diversity of internal granules. They are responsible for functions related to hemostasis, coagulation, and inflammation. The activation of these processes depends on a cascade coordinated by cytokines, chemokines, and components of purinergic signaling, such as ATP, ADP, and adenosine. Platelets express distinct components of the purinergic system: P2X1, P2Y1, PY12, and P2Y14 receptors; and the ectonucleotidases NTPDase, NPP, and 5NTE (ecto-5'-nucleotidase). Except for P2Y14, which has not yet exhibited a known function, all other components relate to the biological processes mentioned before. Platelets are known to display specific responses to microorganisms, being capable of recognizing pathogen-associated molecular patterns (PAMPs), engulfing certain classes of viruses, and participating in NETosis. Platelet function dysregulation implicates various pathophysiological processes, including cardiovascular diseases (CVDs) and infections. In COVID-19 patients, platelets exhibit altered purinergic signaling and increased activation, contributing to inflammation. Excessive platelet activation can lead to complications from thrombosis, which can affect the circulation of vital organs. Therefore, controlling the activation is necessary to end the inflammatory process and restore homeostasis. Ectonucleotidases, capable of hydrolyzing ATP, ADP, and AMP, are of fundamental importance in activating platelets, promising pharmacological targets for clinical use as cardiovascular protective drugs. In this review, we revisit platelet biology, the purinergic receptors and ectonucleotidases on their surface, and their importance in platelet activity. Additionally, we describe methods for isolating platelets in humans and murine, as well as the main techniques for detecting the activity of ectonucleotidases in platelets. Considering the multitude of functions revealed by platelets and their potential use as potent bioreactors able to secrete and present molecules involved in the communication of the vasculature with the immune system, it is crucial to deeply understand platelet biology and purinergic signaling participation to contribute to the developing of therapeutic strategies in diseases of the cardiovascular, inflammatory, and immune systems.

摘要

血小板是具有多种内部颗粒的细胞去核碎片。它们负责与止血、凝血和炎症相关的功能。这些过程的激活取决于细胞因子、趋化因子和嘌呤能信号成分(如 ATP、ADP 和腺苷)协调的级联反应。血小板表达独特的嘌呤能系统成分:P2X1、P2Y1、PY12 和 P2Y14 受体;以及核苷酸酶 NTPDase、NPP 和 5NTE(外核苷酸酶)。除了尚未表现出已知功能的 P2Y14 外,所有其他成分都与前面提到的生物学过程有关。已知血小板对微生物表现出特定的反应,能够识别病原体相关分子模式(PAMPs),吞噬某些类别的病毒,并参与 NETosis。血小板功能失调涉及多种病理生理过程,包括心血管疾病(CVDs)和感染。在 COVID-19 患者中,血小板表现出改变的嘌呤能信号和增加的激活,导致炎症。血小板过度激活可导致血栓形成并发症,从而影响重要器官的循环。因此,控制激活对于结束炎症过程和恢复体内平衡是必要的。能够水解 ATP、ADP 和 AMP 的外核苷酸酶在激活血小板方面具有重要意义,是作为心血管保护药物临床应用的有前途的药理学靶点。在这篇综述中,我们重新审视了血小板生物学、表面的嘌呤能受体和外核苷酸酶及其在血小板活性中的重要性。此外,我们描述了在人类和鼠类中分离血小板的方法,以及检测血小板中外核苷酸酶活性的主要技术。考虑到血小板所揭示的多种功能及其作为能够分泌和呈现参与血管与免疫系统通讯的分子的有效生物反应器的潜在用途,深入了解血小板生物学和嘌呤能信号参与对于开发心血管、炎症和免疫系统疾病的治疗策略至关重要。

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