急性早幼粒细胞白血病与粗内质网相关的巨包涵体发育成小体。

IF 1.5 Q3 HEMATOLOGY
Yong-Xin Ru, Shu-Xu Dong, Jing Liu, Brian Eyden
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引用次数: 1

摘要

本文用透射电镜观察了10例急性早幼粒细胞白血病(APL)患者幼幼粒细胞中巨包涵体和奥尔小体的形态,并对其超微结构细胞化学进行了研究。超微结构细胞化学显示,在巨大包涵体、扩大的内质网池、奥尔体和原生颗粒中,髓过氧化物酶反应阳性。透射电镜显示,巨大的包裹体由退化的rER膜包裹,其中一些与Auer体具有相同的特征。我们假设APL早幼粒细胞的er体发育有一个新的起源,即它们起源于过氧化物酶阳性和扩大的rER池,并且初级颗粒直接从这些扩大的rER元素中释放出来,绕过高尔基体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Development of Auer bodies from giant inclusions associated with rough endoplasmic reticulum in acute promyelocytic leukemia.

Development of Auer bodies from giant inclusions associated with rough endoplasmic reticulum in acute promyelocytic leukemia.

Development of Auer bodies from giant inclusions associated with rough endoplasmic reticulum in acute promyelocytic leukemia.

Development of Auer bodies from giant inclusions associated with rough endoplasmic reticulum in acute promyelocytic leukemia.

Giant inclusions and Auer bodies in promyeloblasts were investigated in a study which included transmission electron microscopy (TEM) for morphology and ultrastructural cytochemistry for myeloperoxidase in 10 patients with acute promyelocytic leukemia (APL). Ultrastructural cytochemistry demonstrated positive myeloperoxidase reactivity in giant inclusions, expanded rER cisternae, Auer bodies and primary granules. TEM revealed that giant inclusions were adorned by degenerated rER membrane, some of them sharing features with Auer bodies. We hypothesize a novel origin for Auer body development in promyeloblasts of APL, namely that they originate from peroxidase-positive and expanded rER cisternae, and that primary granules were directly released from these expanded rER elements, bypassing the Golgi apparatus.

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来源期刊
CiteScore
1.70
自引率
0.00%
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审稿时长
10 weeks
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