Center for Excellence in Vascular Biology, Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
J Thromb Haemost. 2014 Nov;12(11):1764-75. doi: 10.1111/jth.12730. Epub 2014 Oct 13.
The paradigm of platelets as mere mediators of hemostasis has long since been replaced by a dual role: hemostasis and inflammation. Now recognized as key players in innate and adaptive immune responses, platelets have the capacity to interact with almost all known immune cells. These platelet-immune cell interactions represent a hallmark of immunity, as they can potently enhance immune cell functions and, in some cases, even constitute a prerequisite for host defense mechanisms such as NETosis. In addition, recent studies have revealed a new role for platelets in immunity: They are ubiquitous sentinels and rapid first-line immune responders, as platelet-pathogen interactions within the vasculature appear to precede all other host defense mechanisms. Here, we discuss recent advances in our understanding of platelets as inflammatory cells, and provide an exemplary review of their role in acute inflammation.
止血和炎症。现在被认为是先天和适应性免疫反应的关键参与者,血小板具有与几乎所有已知免疫细胞相互作用的能力。这些血小板-免疫细胞相互作用是免疫的标志,因为它们可以强有力地增强免疫细胞的功能,在某些情况下,甚至构成宿主防御机制(如 NETosis)的前提条件。此外,最近的研究揭示了血小板在免疫中的新作用:它们是无处不在的哨兵和快速的一线免疫反应者,因为血管内的血小板-病原体相互作用似乎先于所有其他宿主防御机制。在这里,我们讨论了我们对血小板作为炎症细胞的理解的最新进展,并对其在急性炎症中的作用进行了范例式回顾。