Clawson C C, White J G, Repine J E
Am J Pathol. 1978 Sep;92(3):745-53.
The primary defect of the Chédiak-Higashi syndrome (CHS) which links the several known neutrophil abnormalities in this disorder remains enigmatic. In an attempt to clarify the mechanism of one of the abnormalities of CHS neutrophils, ie, chemotactic migration, the effect of filter pore size was examined in the standard Boyden chamber assay. The response of normal neutrophils to a gradient of zymosan-activated serum was not influenced by increasing the filter pore size from 5 to 8 microgram. However, while CHS neutrophils showed a significant reduction in migratory response from the controls with 5-mu filters, the difference was eliminated when 8-mu filters were employed. Again, when an arachidonic acid gradient was used as the stimulus, migration of CHS neutrophils through 8-mu filters equalled that of controls. These findings indicate the intact nature of the surface receptor and motility systems of the CHS neutrophils and further suggest that the previously defined chemotactic defect in these cells can be explained in terms of the mechanical impediment provided by the CHS giant cytoplasmic granules.
切迪阿克-希加希综合征(CHS)的主要缺陷将该疾病中几种已知的中性粒细胞异常联系在一起,但其仍然是个谜。为了阐明CHS中性粒细胞异常之一即趋化性迁移的机制,在标准的博伊登小室试验中检测了滤膜孔径的影响。正常中性粒细胞对酵母聚糖激活血清梯度的反应不受滤膜孔径从5微米增加到8微米的影响。然而,虽然CHS中性粒细胞与使用5微米滤膜的对照组相比迁移反应显著降低,但使用8微米滤膜时差异消失。同样,当以花生四烯酸梯度作为刺激物时,CHS中性粒细胞通过8微米滤膜的迁移与对照组相当。这些发现表明CHS中性粒细胞表面受体和运动系统的完整性,并进一步表明这些细胞中先前定义的趋化缺陷可以用CHS巨大细胞质颗粒提供的机械障碍来解释。