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血小板活化因子(PAF):细胞间相互作用中的信号传导与黏附

Platelet-activating factor (PAF): signalling and adhesion in cell-cell interactions.

作者信息

Zimmerman G A, Elstad M R, Lorant D E, Mclntyre T M, Prescott S M, Topham M K, Weyrich A S, Whatley R E

机构信息

Nora Eccles Harrison Cardiovascular Research and Training Institute, University of Utah, Salt Lake City, Utah.

出版信息

Adv Exp Med Biol. 1996;416:297-304. doi: 10.1007/978-1-4899-0179-8_47.

Abstract

Signalling by PAF is closely linked to adhesive interactions between cells of the inflammatory and vascular systems. It acts as a juxtacrine signal that alters the activity of beta 2 integrins on myeloid leukocytes (Figure 1), and works in concert with P-selectin at the surfaces of endothelial cells (Figure 2 and text). Observations in models of flow and in vivo support the original experiments using cultured endothelium under static conditions that indicated that PAF acts at this vascular interface. P-selectin modifies and integrates signals delivered through the PAF receptor on monocytes (Figure 4). Adhesion via P-selectin and engagement of beta 2 integrins modify signals leading to PAF synthesis (text and Figure 5). The intimate relationship between adhesive events and signalling by PAF may be a critical determinant in its roles in physiologic and pathologic responses.

摘要

血小板活化因子(PAF)信号传导与炎症和血管系统细胞间的黏附相互作用密切相关。它作为一种旁分泌信号,可改变髓系白细胞上β2整合素的活性(图1),并在内皮细胞表面与P-选择素协同发挥作用(图2及正文)。在流动模型和体内进行的观察结果支持了最初在静态条件下使用培养内皮细胞所做的实验,这些实验表明PAF在这个血管界面发挥作用。P-选择素可修饰并整合通过单核细胞上的PAF受体传递的信号(图4)。通过P-选择素的黏附以及β2整合素的结合会改变导致PAF合成的信号(正文及图5)。黏附事件与PAF信号传导之间的密切关系可能是其在生理和病理反应中发挥作用的关键决定因素。

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