Restoration of podosomes and chemotaxis in Wiskott-Aldrich syndrome macrophages following induced expression of WASp

被引:77
作者
Jones, GE [1 ]
Zicha, D
Dunn, GA
Blundell, M
Thrasher, A
机构
[1] Kings Coll London, Randall Ctr, London SE1 1UL, England
[2] Imperial Canc Res Fund, London WC2A 3PX, England
[3] Kings Coll London, MRC, Muscle & Cell Motil Unit, London SE1 1UL, England
[4] UCL, Inst Child Hlth, London WC1N 1EH, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
actin cytoskeleton; podosome; cell migration; cytokine; chemotaxis; WASp;
D O I
10.1016/S1357-2725(01)00162-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:806 / 815
页数:10
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