Millán Jaime, Williams Lynn, Ridley Anne J
Ludwig Institute for Cancer Research, University College London, UK.
Methods Enzymol. 2006;406:643-55. doi: 10.1016/S0076-6879(06)06050-2.
Tissue injury induces release of cytokines that stimulate the expression of adhesion receptors in the endothelial wall of neighboring vessels. These endothelial receptors recruit leukocytes from the bloodstream and facilitate their transendothelial migration (TEM) toward the inflamed area. The molecules involved in leukocyte-endothelium interaction and TEM have been studied in vivo and in vitro over the past 20 years. Human umbilical vein endothelial cells (HUVECs) are a popular in vitro model to analyze TEM, and have been used to investigate the role of Rho GTPases in this process. Here we describe methods to activate HUVECs, to investigate Rho GTPase-activation by the endothelial adhesion receptor ICAM-1, and to inhibit or activate Rho GTPases using C3 transferase or adenoviruses coding for dominant negative or constitutive active Rho GTPases. Finally, we describe how to image and quantitate leukocyte TEM by digital time-lapse microscopy.
组织损伤会诱导细胞因子释放,这些细胞因子会刺激邻近血管内皮壁中黏附受体的表达。这些内皮受体从血液中募集白细胞,并促进它们跨内皮迁移(TEM)至炎症区域。在过去20年中,人们已在体内和体外对参与白细胞-内皮细胞相互作用及TEM的分子进行了研究。人脐静脉内皮细胞(HUVECs)是一种常用于分析TEM的体外模型,并已被用于研究Rho GTPases在此过程中的作用。在此,我们描述了激活HUVECs的方法、研究内皮黏附受体ICAM-1对Rho GTPase的激活作用,以及使用C3转移酶或编码显性负性或组成型活性Rho GTPases的腺病毒抑制或激活Rho GTPases的方法。最后,我们描述了如何通过数字延时显微镜对白细胞TEM进行成像和定量分析。