White J G, Clawson C C
Am J Pathol. 1979 Sep;96(3):781-98.
The giant inclusion anomaly of leukocytes from three patients with the Chédiak-Higashi syndrome (CHS) has been reexamined by the ultrastructural and cytochemical techniques placing emphasis on the monocyte. Contrary to previous assumptions that all CHS leukocytes shared a common form of giant granule with similar mechanisms of formation, it is shown that CHS monocytes contain ring-shaped organelles as their principle manifestation of the disease. These granules consist of a double membrane surrounding a segment of cytoplasm, which may or may not be sequestered from the remaining cytoplasm and which usually contains one or more normal-sized azurophilic granules. The material lying between the double membranes contains the specific reaction products for peroxidase and acid phosphatase. Therefore, the ring-shaped organelles share identity with the azurophilic granules and probably share a common origin with the primary lysosomes. The double-ring form of giant CHS organelle has also been found infrequently in neutrophils, eosinophils, and lymphocytes.
利用超微结构和细胞化学技术,重点研究单核细胞,对3例患有切-希二氏综合征(CHS)患者白细胞的巨大包涵体异常进行了重新检查。与之前认为所有CHS白细胞都具有共同形式的巨大颗粒且形成机制相似的假设相反,研究表明CHS单核细胞含有环形细胞器,这是该疾病的主要表现形式。这些颗粒由围绕一段细胞质的双层膜组成,这段细胞质可能与其余细胞质隔离,也可能没有,并且通常含有一个或多个正常大小的嗜天青颗粒。双层膜之间的物质含有过氧化物酶和酸性磷酸酶的特异性反应产物。因此,环形细胞器与嗜天青颗粒具有同一性,并且可能与初级溶酶体有共同的起源。巨大的CHS细胞器的双环形式在中性粒细胞、嗜酸性粒细胞和淋巴细胞中也很少见。