Jones Gareth E, Zicha Daniel, Dunn Graham A, Blundell Mike, Thrasher Adrian
The Randall Centre, King's College London, London SE1 1UL, UK.
Int J Biochem Cell Biol. 2002 Jul;34(7):806-15. doi: 10.1016/s1357-2725(01)00162-5.
We used a direct-viewing (Dunn) chemotaxis chamber to analyse the chemotactic responses of human normal and Wiskott-Aldrich syndrome (WAS) macrophages to the cytokine colony stimulating factor-1 (CSF-1). In five patients with classic WAS, where specialised adhesion complexes called podosomes are absent, chemotaxis of macrophages was abolished. The deficient chemotactic responses of WAS macrophages following cytokine stimulation could be correlated with abnormalities in cell polarisation and actin organisation. In a series of cell microinjection studies we found that normal chemotactic responses were restored in WASp macrophages transfected with a full-length human WAS construct. Expression of exogenous WAS protein (WASp) in these cells also restored normal polarised cell morphology and the ability to form podosomes.
我们使用直视(邓恩)趋化性小室来分析人类正常巨噬细胞和威斯科特-奥尔德里奇综合征(WAS)巨噬细胞对细胞因子集落刺激因子-1(CSF-1)的趋化反应。在五名患有典型WAS的患者中,不存在称为足体的特殊粘附复合物,巨噬细胞的趋化性被消除。细胞因子刺激后WAS巨噬细胞趋化反应不足可能与细胞极化和肌动蛋白组织异常有关。在一系列细胞显微注射研究中,我们发现用全长人类WAS构建体转染的WASp巨噬细胞恢复了正常趋化反应。这些细胞中外源性WAS蛋白(WASp)的表达也恢复了正常的极化细胞形态和形成足体的能力。