White J G, Clawson C C
Am J Pathol. 1980 Jan;98(1):151-96.
Defective bactericidal functioning of polymorphonuclear leukocytes (PMNs) from patients with the Chédiak-Higashi syndrome (CHS) has been related in previous reports to a failure of the giant granules characteristics of the disorder to participate in degranulation after uptake of foreign particulates by neutrophils. However, the reason massive CHS inclusions do not fuse with and discharge their contents into phagocytic vacuoles has not been defined. The problem is particularly puzzling because it has been postulated that the hugh organelles in CHS neutophils originate by fusion of small azurophilic granules in promyelocytes and myelocytes. The present series of investigations into the cytopathology of the CHS has employed electron microscopy and ultrastructural cytochemistry to characterize the progressive enlargement of the hugh bodies in mature PMNs, their interaction with cytoplasmic constituents resulting in various manifestations of cell injury, and their response to foreign particulates. Each study clarifies abnormal features of the giant organelles essential to the understanding of their role in the defective bactericidal function of CHS neutrophils. The first report demonstrates that most of the hugh inclusions in PMNs are not primary lysosomes. The interaction and fusion of giant azurophilic granules with each other, with normal-sized primary and secondary granules, and with cytoplasmic components converts the massive primary granules into huge secondary lysosomes. Transformation to secondary hysosomes represents a critical alteration in the state of the giant granules that underlies their damaging influence on the cytoplasm and loss of reactivity wtih phagocytic vacuoles.
先前的报告指出,患有切-东综合征(CHS)患者的多形核白细胞(PMN)杀菌功能存在缺陷,这与该病症的巨大颗粒在被中性粒细胞摄取外来颗粒后未能参与脱颗粒有关。然而,大量CHS内含物不与吞噬泡融合并将其内容物释放到吞噬泡中的原因尚未明确。这个问题尤其令人困惑,因为据推测,CHS中性粒细胞中的巨大细胞器起源于早幼粒细胞和中幼粒细胞中小的嗜天青颗粒的融合。本系列对CHS细胞病理学的研究采用了电子显微镜和超微结构细胞化学技术,以表征成熟PMN中巨大体的逐渐增大、它们与细胞质成分的相互作用导致的各种细胞损伤表现以及它们对外来颗粒的反应。每项研究都阐明了巨大细胞器的异常特征,这对于理解它们在CHS中性粒细胞杀菌功能缺陷中的作用至关重要。第一篇报告表明,PMN中的大多数巨大内含物不是初级溶酶体。巨大嗜天青颗粒彼此之间、与正常大小的初级和次级颗粒以及与细胞质成分的相互作用和融合,将大量初级颗粒转化为巨大的次级溶酶体。向次级溶酶体的转变代表了巨大颗粒状态的关键改变,这是它们对细胞质产生破坏影响以及与吞噬泡失去反应性的基础。