先天性II型促红细胞增生性贫血红细胞的超微结构特征,以外周池和双膜为重点。

IF 1.5 Q3 HEMATOLOGY 血液科学(英文) Pub Date : 2023-01-01 DOI:10.1097/BS9.0000000000000136
Yong-Xin Ru, Shu-Xu Dong, Jing Liu, Brian Eyden
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引用次数: 0

摘要

红细胞外周池和双膜(PCDMs)是II型先天性促红细胞生成性贫血(CDA)的标志。为了进一步了解红细胞生成的机制,我们用透射电镜研究了22例中国CDAⅡ患者骨髓中的红细胞和红细胞。该研究表明,随着原红细胞向红细胞的发展,所有患有pcdm的患者的红细胞都增加了。pcdm常与内质网池和核周间隙相连,伴多染和正染红细胞核固缩、核溶解和破坏。结果表明,pcdm在红细胞生成过程中由内质网转化,并参与CDA II患者晚期红细胞的溶解和缺失。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Ultrastructural characteristics of erythroid cells in congenital dyserythropoietic anemia type II, with a focus on peripheral cisternae and double membranes.

Peripheral cisternae and double membranes (PCDMs) in erythroid cells are a landmark of type II congenital dyserythropoietic anemia (CDA). To gain further insights into the mechanism of dyserythropoiesis, erythroblasts and erythrocytes in bone marrow were studied in 22 Chinese patients with CDA Ⅱ by transmission electron microscopy. The study demonstrated an increase in all patients in erythroblasts with PCDMs with development from pro-erythroblast to red blood cells. PCDMs often connected with cisternae of endoplasmic reticulum (ER) and the perinuclear space, and were accompanied by karyopyknosis, karyolysis and disruption in polychromatic and orthochromatic erythroblasts. The results suggest that PCDMs are transformed from ER during erythropoiesis and participate in the dissolution and deletion of late erythroid cells in patients with CDA II.

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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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