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慢性粒细胞白血病中血液中性粒细胞的嗜天青颗粒和特异性颗粒:超微结构和细胞化学分析

Azurophil and specific granules of blood neutrophils in chronic myelogenous leukemia: an ultrastructural and cytochemical analysis.

作者信息

Ullyot J L, Bainton D F

出版信息

Blood. 1975 Apr;45(4):469-82.

PMID:1054264
Abstract

That most patients with chronic myelogenous leukemia (CML) have either very low levels or no leukocyte alkaline phosphatase activity (LAP) is an established fact. In view of our new findings7 that normal mature human polymorphonuclear leukocytes (PMN) contain two types of granules, azurophils (1/3) and specifics (2/3), and that alkaline phosphatase is present only in specific granules, we undertook the present studies to determine whether these neoplastic PMN lack a specific granule population or simply lack the enzyme. The cellular buffy coats of five patients with CML (Ph1 plus, LAP minus) were fixed in glutaraldehyde, incubated for peroxidase to identify the azurophil population, and examined by electron microscopy. It was found that the specific granule population was present in all mature PMN. Counts of both azurophil and specific granules per cell were slightly lower than normal but were within an 80%-90% overlap of the normal range. We therefore conclude that the low level of LAP in patients with CML reflects a deficiency of the enzyme rather than a missing granule population. Although the mature PMN appeared relatively normal (with few exceptions), circulating myeloblasts and promyelocytes revealed several abnormalities, the most notable being the presence of large bundles of cytoplasmic microfilaments. The blood of two patients in the terminal phase of disease was reexamined. Most of their cells were immature, with aberrations similar to those in myeloblasts and promyelocytes in the chronic phase of the disorder. In addition, however, we discovered three adnormal populations of mature PMN: (1) PMN containing both populations of granules but lacking peroxidase, (2) PMN lacking specific granules, and (3) PMN lacking azurophil granules. Our findings emphasize the value of electron microscopy and cytochemistry in detecting abnormalities of maturation in the cytoplasm of leukemic PMN.

摘要

大多数慢性粒细胞白血病(CML)患者的白细胞碱性磷酸酶活性(LAP)要么极低,要么完全没有,这是一个既定事实。鉴于我们的新发现7,即正常成熟的人类多形核白细胞(PMN)含有两种类型的颗粒,嗜天青颗粒(1/3)和特异性颗粒(2/3),且碱性磷酸酶仅存在于特异性颗粒中,我们开展了本研究,以确定这些肿瘤性PMN是缺乏特定颗粒群体,还是仅仅缺乏该酶。对5例CML患者(Ph1阳性,LAP阴性)的细胞血沉棕黄层进行戊二醛固定,用过氧化物酶孵育以识别嗜天青颗粒群体,然后进行电子显微镜检查。结果发现,所有成熟的PMN中都存在特异性颗粒群体。每个细胞的嗜天青颗粒和特异性颗粒计数均略低于正常水平,但仍在正常范围的80%-90%重叠范围内。因此,我们得出结论,CML患者LAP水平低反映的是酶的缺乏,而非颗粒群体的缺失。尽管成熟的PMN相对正常(少数例外),但循环中的原始粒细胞和早幼粒细胞显示出一些异常,最显著的是存在大量成束的细胞质微丝。对两名处于疾病终末期患者的血液进行了重新检查。他们的大多数细胞不成熟,具有与该疾病慢性期原始粒细胞和早幼粒细胞相似的畸变。然而,此外,我们还发现了三种异常的成熟PMN群体:(1)含有两种颗粒群体但缺乏过氧化物酶的PMN;(2)缺乏特异性颗粒的PMN;(3)缺乏嗜天青颗粒的PMN。我们的发现强调了电子显微镜和细胞化学在检测白血病PMN细胞质成熟异常方面的价值。

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