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血小板 BTK 在肺炎链球菌性肺炎脓毒症期间维持肺血管完整性中是必需的。

Platelet Btk is Required for Maintaining Lung Vascular Integrity during Murine Pneumococcal Pneumosepsis.

机构信息

Center for Experimental and Molecular Medicine (CEMM), Amsterdam UMC, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.

Amsterdam Infection and Immunity Institute (AI&II), Amsterdam UMC, Amsterdam, The Netherlands.

出版信息

Thromb Haemost. 2019 Jun;119(6):930-940. doi: 10.1055/s-0039-1681046. Epub 2019 Mar 14.

Abstract

Platelet Bruton's tyrosine kinase (Btk) is an essential signalling protein for the collagen receptor glycoprotein VI (GPVI) and podoplanin receptor C-type-lectin-like receptor-2, which are platelet receptors implicated in the maintenance of vascular integrity during inflammation. Moreover, platelets, platelet GPVI and Btk are important for host defence during murine bacterial pneumosepsis. The aim of this study was to determine the role of platelet Btk in vascular integrity and host defence during murine pneumosepsis caused by the common human pathogens and . Using the Cre-loxP system, male platelet-specific Btk-deficient mice (PF4creBtk/Y) were created. Similar to platelets from total Btk-deficient mice, platelets from PF4creBtk/Y mice showed abrogated aggregation and P-selectin expression when stimulated with the GPVI ligand cross-linked collagen-related peptide. Upon infection with , PF4creBtk/Y mice showed increased lung bleeding, but unimpaired anti-bacterial defence. During pneumosepsis evoked by , platelet Btk deficiency was not associated with lung bleeding and did not impact on host defence, even when platelet function was further compromised by blocking secondary platelet activation by the P2Y receptor antagonist clopidogrel. Together, these data indicate that, while platelet Btk is not important for anti-bacterial defence in pneumosepsis, its role in maintaining vascular integrity in the lung depends on the causative pathogen.

摘要

血小板布鲁顿酪氨酸激酶 (Btk) 是胶原蛋白受体糖蛋白 VI (GPVI) 和 podoplanin 受体 C 型凝集素样受体-2 的必需信号蛋白,这些血小板受体参与炎症过程中血管完整性的维持。此外,血小板、血小板 GPVI 和 Btk 在小鼠细菌性肺炎败血症的宿主防御中也很重要。本研究旨在确定血小板 Btk 在由常见人类病原体 和 引起的小鼠肺炎败血症中的血管完整性和宿主防御中的作用。使用 Cre-loxP 系统,创建了雄性血小板特异性 Btk 缺陷小鼠 (PF4creBtk/Y)。与来自总 Btk 缺陷小鼠的血小板相似,当用交联的胶原相关肽刺激 GPVI 配体时,来自 PF4creBtk/Y 小鼠的血小板显示出聚集和 P-选择素表达的阻断。在感染 后,PF4creBtk/Y 小鼠表现出增加的肺出血,但抗细菌防御不受影响。在由 引起的肺炎败血症中,血小板 Btk 缺乏与肺出血无关,也不影响宿主防御,即使通过阻断 P2Y 受体拮抗剂氯吡格雷对血小板的二次激活来进一步损害血小板功能。总之,这些数据表明,虽然血小板 Btk 在肺炎败血症中的抗细菌防御中不重要,但它在维持肺血管完整性中的作用取决于致病病原体。

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