Oliver J M
Am J Pathol. 1978 Oct;93(1):221-70.
In this review I have attempted to explain the processes of chemotaxis, phagocytosis, oxidant generation, and lysosomal degranulation in normal and genetically abnormal human PMN. In my view these leukocyte functions are most importantly dependent on the integrity of three cellular components: the plasma membrane, the submembranous microfilaments, and the cytoplasmic microtubules. These components are often discussed in isolation, and the biochemical and pharmacological aspects of their function are analyzed separately here. However, PMN motile and bactericidal activities require the interdependent functioning of membranes, microtubules, and microfilaments. I have therefore tried to provide an integrated view of cytoskeleton-membrane organization and function in human PMN. I have particularly emphasized dynamic aspects of the cytoskeleton and membranes, eg, the induction of microtubule assembly and membrane enzyme activation by surface ligands and the reorganization of microfilaments in response to the same ligands. With this background established, I have selected for discussion a series of diseases in which abnormalities of chemotaxis, phagocytosis, lysosomal degranulation, and/or oxidant generation can be explained directly or indirectly by abnormalities in dynamic properties of PMN membranes, microtubules, or microfilaments. I emphasize that even preliminary insight into the basis of these disorders has sometimes been sufficient to suggest useful clinical approaches to the management of patients. In several of these neutrophil abnormalities, ie, neutrophil actin dysfunction, Chédiak-Higashi syndrome, and its "antithesis" described by Gallin and co-workers, the cellular dysfunctions were well documented but the molecular basis was completely obscure prior to cell biologic analysis. Snyderman and Pike 159 and Chusid and co-workers 160 emphasized the existence of a large number of other neutrophil bactericidal abnormalities resulting from as yet unexplained cellular defects. Further analyses of the functional interactions between membranes and cytoskeletal components in neutrophils may not only clarify the molecular bases of the disorders described here but also may provide insight into the origins and proper therapeutic approach to other granulocyte dysfunctions.
在这篇综述中,我试图解释正常和基因异常的人类中性粒细胞的趋化作用、吞噬作用、氧化剂生成及溶酶体脱颗粒的过程。在我看来,这些白细胞功能最重要地依赖于三种细胞成分的完整性:质膜、膜下微丝和细胞质微管。这些成分常常被单独讨论,在此分别分析其功能的生化和药理学方面。然而,中性粒细胞的运动和杀菌活性需要膜、微管和微丝的相互依存作用。因此,我试图提供关于人类中性粒细胞细胞骨架 - 膜组织和功能的综合观点。我特别强调了细胞骨架和膜的动态方面,例如表面配体诱导微管组装和膜酶激活以及微丝对相同配体的重组反应。在此背景下,我选择讨论一系列疾病,其中趋化作用、吞噬作用、溶酶体脱颗粒和/或氧化剂生成异常可直接或间接由中性粒细胞膜、微管或微丝的动态特性异常来解释。我强调,即使对这些疾病基础的初步了解有时也足以提示对患者管理有用的临床方法。在这些中性粒细胞异常中的几种情况,即中性粒细胞肌动蛋白功能障碍、Chédiak - Higashi综合征以及Gallin及其同事描述的其“对立面”,细胞功能障碍有充分记录,但在细胞生物学分析之前分子基础完全不清楚。Snyderman和Pike 159以及Chusid及其同事160强调存在大量其他由尚未解释的细胞缺陷导致的中性粒细胞杀菌异常。对中性粒细胞中膜与细胞骨架成分之间功能相互作用的进一步分析不仅可能阐明此处所述疾病的分子基础,而且可能为其他粒细胞功能障碍的起源和适当治疗方法提供见解。