Sennett Christopher, Pula Giordano
Biomedical Institute for Multimorbidity (BIM), Hull York Medical School (HYMS), University of Hull, Hull HU6 7RX, UK.
Cells. 2025 Feb 25;14(5):335. doi: 10.3390/cells14050335.
Neutrophil extracellular traps (NETs) have received significant attention in recent years for their role in both the immune response and the vascular damage associated with inflammation. Platelets have been described as critical components of NETs since the initial description of this physio-pathological response of neutrophils. Platelets have been shown to play a dual role as responders and also as stimulators of NETs. The direct interaction with DNA leads to the entrapment of platelets into NETs, a phenomenon that significantly contributes to the thrombotic complications of inflammation and neutrophil activation, while the direct and paracrine stimulation of neutrophils by platelets has been shown to initiate the process of NET formation. In this review, we provide a comprehensive description of our current understanding of the molecular mechanisms underlying the entrapping of platelets into NETs and, in parallel, the platelet-driven cellular responses promoting NET formation. We then illustrate established examples of the contribution of NETs to vascular pathologies, describe the important questions that remain to be answered regarding the contribution of platelets to NET formation and NET-dependent cardiovascular complication, and highlight the fundamental steps taken towards the application of our understanding of platelets' contribution to NETs for the development of novel cardiovascular therapies.
近年来,中性粒细胞胞外陷阱(NETs)因其在免疫反应以及与炎症相关的血管损伤中的作用而受到广泛关注。自对中性粒细胞这种生理病理反应进行首次描述以来,血小板就被认为是NETs的关键组成部分。血小板已被证明在NETs中扮演双重角色,既是反应者,也是NETs的刺激者。与DNA的直接相互作用会导致血小板被困在NETs中,这一现象显著促成了炎症和中性粒细胞活化的血栓形成并发症,而血小板对中性粒细胞的直接和旁分泌刺激已被证明可启动NET形成过程。在这篇综述中,我们全面阐述了目前对血小板被困在NETs中的分子机制的理解,同时也阐述了血小板驱动的促进NET形成的细胞反应。然后,我们举例说明了NETs对血管病变的作用,描述了关于血小板对NET形成和NET依赖性心血管并发症的作用仍有待解答的重要问题,并强调了在将我们对血小板在NETs中作用的理解应用于开发新型心血管疗法方面所迈出的基本步骤。