Lorenzon P, Vecile E, Nardon E, Ferrero E, Harlan J M, Tedesco F, Dobrina A
Department of Physiology and Pathology, University of Trieste, Trieste, Italy.
J Cell Biol. 1998 Sep 7;142(5):1381-91. doi: 10.1083/jcb.142.5.1381.
Previous studies have shown that polymorphonuclear leukocyte (PMN) adherence to endothelial cells (EC) induces transient increases in EC cytosolic free calcium concentration ([Ca2+]i) that are required for PMN transit across the EC barrier (Huang, A.J., J.E. Manning, T. M. Bandak, M.C. Ratau, K.R. Hanser, and S.C. Silverstein. 1993. J. Cell Biol. 120:1371-1380). To determine whether stimulation of [Ca2+]i changes in EC by leukocytes was induced by the same molecules that mediate leukocyte adherence to EC, [Ca2+]i was measured in Fura2-loaded human EC monolayers. Expression of adhesion molecules by EC was induced by a pretreatment of the cells with histamine or with Escherichia coli lipopolysaccharide (LPS), and [Ca2+]i was measured in single EC after the addition of mAbs directed against the EC adhesion proteins P-selectin, E-selectin, intercellular adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1), or platelet/endothelial cell adhesion molecule-1 (PECAM-1). Both anti-P- and anti-E-selectin mAb, as well as anti-VCAM-1 mAb, induced transient increases in EC [Ca2+]i that were comparable to those induced by 200 microM histamine. In contrast, no effect was obtained by mAbs directed against the endothelial ICAM-1 or PECAM-1. PMN adherence directly stimulated increases in [Ca2+]i in histamine- or LPS-treated EC. mAbs directed against leukocyte CD18 or PECAM-1, the leukocyte counter-receptors for endothelial ICAM-1 and PECAM-1, respectively, did not inhibit PMN-induced EC activation. In contrast, mAb directed against sialyl Lewis x (sLex), a PMN ligand for endothelial P- and E-selectin, completely inhibited EC stimulation by adherent PMN. Changes in EC [Ca2+]i were also observed after adherence of peripheral blood monocytes to EC treated with LPS for 5 or 24 h. In these experiments, the combined addition of mAbs to sLex and VLA-4, the leukocyte counter-receptor for endothelial VCAM-1, inhibited [Ca2+]i changes in the 5 h-treated EC, whereas the anti-VLA-4 mAb alone was sufficient to inhibit [Ca2+]i changes in the 24 h-treated EC. Again, no inhibitory effect was observed with an anti-CD18 or anti-PECAM-1 mAb. Of note, the conditions that induced changes in EC [Ca2+]i, i.e. , mAbs directed against endothelial selectins or VCAM-1, and PMN or monocyte adhesion to EC via selectins or VCAM-1, but not via ICAM-1 or PECAM-1, also induced a rearrangement of EC cytoskeletal microfilaments from a circumferential ring to stress fibers. We conclude that, in addition to their role as adhesion receptors, endothelial selectins and VCAM-1 mediate endothelial stimulation by adhering leukocytes.
先前的研究表明,多形核白细胞(PMN)与内皮细胞(EC)的黏附会导致EC胞质游离钙浓度([Ca2+]i)短暂升高,这是PMN穿过EC屏障所必需的(Huang, A.J., J.E. Manning, T.M. Bandak, M.C. Ratau, K.R. Hanser, and S.C. Silverstein. 1993. J. Cell Biol. 120:1371 - 1380)。为了确定白细胞对EC中[Ca2+]i变化的刺激是否由介导白细胞与EC黏附的相同分子所诱导,在装载了Fura2的人EC单层中测量了[Ca2+]i。通过用组胺或大肠杆菌脂多糖(LPS)预处理细胞来诱导EC黏附分子的表达,在添加针对EC黏附蛋白P - 选择素、E - 选择素、细胞间黏附分子 - 1(ICAM - 1)、血管细胞黏附分子 - 1(VCAM - 1)或血小板/内皮细胞黏附分子 - 1(PECAM - 1)的单克隆抗体(mAb)后,测量单个EC中的[Ca2+]i。抗P - 选择素和抗E - 选择素mAb以及抗VCAM - 1 mAb均诱导EC [Ca2+]i短暂升高,其幅度与200微摩尔组胺所诱导的相当。相反,针对内皮ICAM - 1或PECAM - 1的mAb未产生影响。PMN黏附直接刺激组胺或LPS处理的EC中[Ca2+]i升高。分别针对内皮ICAM - 1和PECAM - 1的白细胞对应受体白细胞CD18或PECAM - 1的mAb,并不抑制PMN诱导的EC活化。相反,针对唾液酸化路易斯x(sLex)的mAb,一种内皮P - 选择素和E - 选择素的PMN配体,完全抑制黏附的PMN对EC的刺激。在用LPS处理5或24小时的EC上,外周血单核细胞黏附后也观察到EC [Ca2+]i的变化。在这些实验中,联合添加针对sLex和VLA - 4(内皮VCAM - 1的白细胞对应受体)的mAb,可抑制5小时处理的EC中[Ca2+]i的变化,而单独的抗VLA - 4 mAb足以抑制24小时处理的EC中[Ca2+]i的变化。同样,抗CD18或抗PECAM - 1 mAb未观察到抑制作用。值得注意的是,诱导EC [Ca2+]i变化的条件,即针对内皮选择素或VCAM - 1的mAb,以及PMN或单核细胞通过选择素或VCAM - 1而非ICAM - 1或PECAM - 1与EC的黏附,也诱导了EC细胞骨架微丝从周向环向应力纤维的重排。我们得出结论,除了作为黏附受体的作用外,内皮选择素和VCAM - 1还通过黏附的白细胞介导内皮刺激。