ACRF Department of Cancer Biology and Therapeutics, The John Curtin School of Medical Research, The Australian National University, Canberra, ACT, Australia.
Research School of Electrical, Energy and Materials Engineering, The Australian National University, Canberra, ACT, Australia.
Front Immunol. 2020 Jan 31;11:78. doi: 10.3389/fimmu.2020.00078. eCollection 2020.
Platelets are small anucleate cells that are essential for many biological processes including hemostasis, thrombosis, inflammation, innate immunity, tumor metastasis, and wound healing. Platelets circulate in the blood and in order to perform all of their biological roles, platelets must be able to arrest their movement at an appropriate site and time. Our knowledge of how platelets achieve this has expanded as our ability to visualize and quantify discreet platelet events has improved. Platelets are exquisitely sensitive to changes in blood flow parameters and so the visualization of rapid intricate platelet processes under conditions found in flowing blood provides a substantial challenge to the platelet imaging field. The platelet's size (~2 μm), rapid activation (milliseconds), and unsuitability for genetic manipulation, means that appropriate imaging tools are limited. However, with the application of modern imaging systems to study platelet function, our understanding of molecular events mediating platelet adhesion from a single-cell perspective, to platelet recruitment and activation, leading to thrombus (clot) formation has expanded dramatically. This review will discuss current platelet imaging techniques and , describing how the advancements in imaging have helped answer/expand on platelet biology with a particular focus on hemostasis. We will focus on platelet aggregation and thrombus formation, and how platelet imaging has enhanced our understanding of key events, highlighting the knowledge gained through the application of imaging modalities to experimental models and . Furthermore, we will review the limitations of current imaging techniques, and questions in thrombosis research that remain to be addressed. Finally, we will speculate how the same imaging advancements might be applied to the imaging of other vascular cell biological functions and visualization of dynamic cell-cell interactions.
血小板是无核的小细胞,对于许多生物学过程至关重要,包括止血、血栓形成、炎症、先天免疫、肿瘤转移和伤口愈合。血小板在血液中循环,为了发挥其所有生物学作用,血小板必须能够在适当的部位和时间停止其运动。随着我们可视化和量化离散血小板事件的能力的提高,我们对血小板如何实现这一目标的了解也在不断扩大。血小板对血流参数的变化非常敏感,因此在流动血液中发现的条件下观察快速复杂的血小板过程对血小板成像领域提出了巨大挑战。血小板的大小(~2 μm)、快速激活(毫秒级)和不适合遗传操作,意味着适当的成像工具是有限的。然而,随着现代成像系统在研究血小板功能中的应用,我们对介导血小板黏附的分子事件的理解从单细胞角度扩展到血小板募集和激活,导致血栓(凝块)形成。这篇综述将讨论当前的血小板成像技术,并描述成像技术的进步如何帮助从单个细胞的角度回答/扩展血小板生物学,特别关注止血。我们将重点讨论血小板聚集和血栓形成,以及血小板成像如何增强我们对关键事件的理解,强调通过将成像模式应用于实验模型获得的知识。此外,我们将回顾当前成像技术的局限性,以及血栓形成研究中仍待解决的问题。最后,我们将推测同样的成像进展如何应用于其他血管细胞生物学功能的成像和动态细胞-细胞相互作用的可视化。