Nieto M, Frade J M, Sancho D, Mellado M, Martinez-A C, Sánchez-Madrid F
Servicio de Inmunología, Hospital de la Princesa, Universidad Autónoma de Madrid, E-28006, Madrid, Spain.
J Exp Med. 1997 Jul 7;186(1):153-8. doi: 10.1084/jem.186.1.153.
Leukocyte migration in response to cell attractant gradients or chemotaxis is a key phenomenon both in cell movement and in the inflammatory response. Chemokines are quite likely to be the key molecules directing migration of leukocytes that involve cell polarization with generation of specialized cell compartments. The precise mechanism of leukocyte chemoattraction is not known, however. In this study, we demonstrate that the CC chemokine receptors CCR2 and CCR5, but not cytokine receptors such as interleukin (IL)-2Ralpha, IL-2Rbeta, tumor necrosis factor receptor 1, or transforming growth factor betaR, are redistributed to a pole in T cells that are migrating in response to chemokines. Immunofluorescence and confocal microscopy studies show that the chemokine receptors concentrate at the leading edge of the cell on the flattened cell-substratum contact area, induced specifically by the signals that trigger cell polarization. The redistribution of chemokine receptors is blocked by pertussis toxin and is dependent on cell adhesion through integrin receptors, which mediate cell migration. Chemokine receptor expression on the leading edge of migrating polarized lymphocytes appears to act as a sensor mechanism for the directed migration of leukocytes through a chemoattractant gradient.
白细胞对细胞吸引剂梯度的迁移或趋化作用是细胞运动和炎症反应中的关键现象。趋化因子很可能是指导白细胞迁移的关键分子,这涉及到细胞极化以及特殊细胞区室的形成。然而,白细胞化学吸引的确切机制尚不清楚。在本研究中,我们证明CC趋化因子受体CCR2和CCR5,而非细胞因子受体如白细胞介素(IL)-2Rα、IL-2Rβ、肿瘤坏死因子受体1或转化生长因子βR,会重新分布到响应趋化因子而迁移的T细胞的一极。免疫荧光和共聚焦显微镜研究表明,趋化因子受体集中在扁平细胞 - 基质接触区域的细胞前缘,这是由触发细胞极化的信号特异性诱导的。趋化因子受体的重新分布被百日咳毒素阻断,并且依赖于通过整合素受体的细胞黏附,整合素受体介导细胞迁移。迁移的极化淋巴细胞前缘的趋化因子受体表达似乎作为一种传感机制,通过化学吸引剂梯度指导白细胞的定向迁移。