Sullivan David P, Watson Richard L, Muller William A
Department of Pathology, Feinberg School of Medicine, Chicago, Illinois.
Department of Pathology, Feinberg School of Medicine, Chicago, Illinois
Am J Physiol Heart Circ Physiol. 2016 Sep 1;311(3):H621-32. doi: 10.1152/ajpheart.00289.2016. Epub 2016 Jul 15.
Leukocyte transendothelial migration (TEM) is an essential component of the inflammatory response. In vitro studies with human cells have demonstrated that platelet/endothelial cell adhesion molecule (PECAM) functions upstream of CD99 during TEM; however, results in vivo with mice have been apparently contradictory. In this study we use four-dimensional (4D) intravital microscopy to demonstrate that the site and order of function of PECAM and CD99 in vivo are dependent on the strain of mice. In FVB/n mice, PECAM functions upstream of CD99, as in human cells in vitro, and blocking antibodies against either molecule arrest neutrophils before they traverse the endothelium. However, in C57BL/6 mice, PECAM and CD99 appear to function at a different step, as the same antibodies arrest leukocyte migration through the endothelial basement membrane. These results are the first direct comparison of PECAM and CD99 function in different murine strains as well as the first demonstration of the sequential function of PECAM and CD99 in vivo.
白细胞跨内皮迁移(TEM)是炎症反应的一个重要组成部分。对人类细胞的体外研究表明,在TEM过程中血小板/内皮细胞黏附分子(PECAM)在CD99的上游发挥作用;然而,在小鼠体内的研究结果显然相互矛盾。在本研究中,我们使用四维(4D)活体显微镜来证明体内PECAM和CD99的功能位点和顺序取决于小鼠品系。在FVB/n小鼠中,PECAM在CD99的上游发挥作用,就像在体外人类细胞中一样,针对这两种分子的阻断抗体在中性粒细胞穿过内皮之前就会阻止它们。然而,在C57BL/6小鼠中,PECAM和CD99似乎在不同步骤发挥作用,因为相同的抗体可阻止白细胞穿过内皮基底膜。这些结果首次直接比较了不同小鼠品系中PECAM和CD99的功能,也是首次证明体内PECAM和CD99的顺序功能。