Boehme S A, Sullivan S K, Crowe P D, Santos M, Conlon P J, Sriramarao P, Bacon K B
Neurocrine Biosciences, Inc., San Diego, CA 92121, USA.
J Immunol. 1999 Aug 1;163(3):1611-8.
Eotaxin is a potent eosinophil chemoattractant that plays an important role in regulating eosinophil tissue levels both in healthy individuals and in diseases associated with significant eosinophil infiltrates, such as the allergic inflammation observed in asthma. Here, we demonstrate that treatment of eosinophils with eotaxin induces the phosphorylation of the mitogen-activated protein kinases (MAPKs) p42 and p44, leading to kinase activation. Blockade of MAPK activation by the MAPK kinase inhibitor PD98059 leads to a dramatic decrease in eotaxin-induced eosinophil rolling in vivo and chemotaxis in vitro. This blockade in the leukocyte migration process is consistent with the observed inhibition of actin polymerization and rearrangement within the eosinophil following treatment with MAPK inhibitor. It is suggested, therefore, that the intrinsic mechanism of eotaxin-induced eosinophil rolling and migration involves activation of the p42/p44 MAPK, possibly through regulation of the cytoskeletal rearrangements necessary for chemotaxis.
嗜酸性粒细胞趋化因子是一种强效的嗜酸性粒细胞趋化剂,在健康个体以及与显著嗜酸性粒细胞浸润相关的疾病(如哮喘中观察到的过敏性炎症)中,对调节嗜酸性粒细胞组织水平起着重要作用。在此,我们证明用嗜酸性粒细胞趋化因子处理嗜酸性粒细胞会诱导丝裂原活化蛋白激酶(MAPK)p42和p44的磷酸化,从而导致激酶激活。MAPK激酶抑制剂PD98059对MAPK激活的阻断导致嗜酸性粒细胞趋化因子诱导的嗜酸性粒细胞在体内滚动和体外趋化作用显著降低。白细胞迁移过程中的这种阻断与在用MAPK抑制剂处理后嗜酸性粒细胞内观察到的肌动蛋白聚合和重排的抑制相一致。因此,有人提出,嗜酸性粒细胞趋化因子诱导的嗜酸性粒细胞滚动和迁移的内在机制涉及p42/p44 MAPK的激活,可能是通过调节趋化作用所需的细胞骨架重排来实现的。