Tokarz-Deptuła Beata, Baraniecki Łukasz, Palma Joanna, Stosik Michał, Deptuła Wiesław
Institute of Biology, University of Szczecin, 71-412 Szczecin, Poland.
Doctoral School, University of Szczecin, 70-384 Szczecin, Poland.
Int J Mol Sci. 2024 Nov 24;25(23):12611. doi: 10.3390/ijms252312611.
The article characterises platelets, pointing out the role and contribution of their numerous receptors determining their specific and broad immune activity. Three types of platelet receptors are described, that is, extracellular and intracellular receptors-TLR (toll-like receptors), NLR (NOD-like receptor), and RLR (RIG-I-like receptor); extracellular receptors-selectins and integrins; and their other extracellular receptors-CLR (C-type lectin receptor), CD (cluster of differentiation), TNF (tumour necrosis factor), among others. Outlining the contribution of these numerous platelet receptors to the intravascular immunity, it has been shown that they are formed by their fusion with pathogen-associated molecular patterns (PAMPs), damage-associated molecular patterns (DAMPs), and lifestyle-associated molecular patterns (LAMPs). They are initiating and effector components of signal transduction of these cells, and their expression and quantity determine the specific and broad functions of platelets towards influencing vascular endothelial cells, but mainly PRRs (pattern recognition receptors) of blood immune cells. These facts make platelets the fundamental elements that shape not only intravascular homeostasis, as previously indicated, but they become the determinants of immunity in blood vessels. Describing the reactions of the characterised three groups of platelet receptors with PAMP, DAMP and LAMP molecules, the pathways and participation of platelets in the formation and construction of intravascular immune status, in physiological states, but mainly in pathological states, including bacterial and viral infections, are presented, making these cells essential elements in the health and disease of mammals, including humans.
本文对血小板进行了特征描述,指出了其众多受体在决定其特异性和广泛免疫活性方面的作用及贡献。文中描述了三种类型的血小板受体,即细胞外和细胞内受体——Toll样受体(TLR)、NOD样受体(NLR)和RIG-I样受体(RLR);细胞外受体——选择素和整合素;以及其他细胞外受体——C型凝集素受体(CLR)、分化簇(CD)、肿瘤坏死因子(TNF)等。概述了这些众多血小板受体对血管内免疫的贡献,研究表明它们是通过与病原体相关分子模式(PAMP)、损伤相关分子模式(DAMP)和生活方式相关分子模式(LAMP)融合而形成的。它们是这些细胞信号转导的起始和效应成分,其表达和数量决定了血小板对血管内皮细胞,尤其是血液免疫细胞的模式识别受体(PRR)产生影响的特异性和广泛功能。这些事实使血小板不仅如前文所述成为塑造血管内稳态的基本要素,而且还成为血管免疫的决定因素。文中描述了所表征的三组血小板受体与PAMP、DAMP和LAMP分子的反应,介绍了血小板在生理状态下,尤其是在包括细菌和病毒感染在内的病理状态下参与血管内免疫状态形成和构建的途径,这使得这些细胞成为包括人类在内的哺乳动物健康和疾病的关键要素。