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II型先天性红细胞生成异常性贫血中红系细胞的超微结构特征,重点关注外周池和双膜。

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

作者信息

Ru Yong-Xin, Dong Shu-Xu, Liu Jing, Eyden Brian

机构信息

State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of the Cell Ecosystem, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China.

Formerly: Department of Histopathology, Christie Hospital NHS Trust, Manchester, UK.

出版信息

Blood Sci. 2022 Oct 10;5(1):25-31. doi: 10.1097/BS9.0000000000000136. eCollection 2023 Jan.

Abstract

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.

摘要

红系细胞中的外周池和双膜结构(PCDMs)是II型先天性红细胞生成异常性贫血(CDA)的一个标志。为了进一步深入了解红细胞生成异常的机制,我们通过透射电子显微镜对22例中国CDA II型患者的骨髓中的成红细胞和红细胞进行了研究。该研究表明,所有患者中具有PCDMs的成红细胞随着从早幼红细胞到红细胞的发育而增加。PCDMs常与内质网(ER)池和核周间隙相连,并伴有多染性和正染性成红细胞中的核固缩、核溶解和破坏。结果表明,PCDMs在红细胞生成过程中由ER转化而来,并参与CDA II型患者晚期红系细胞的溶解和清除。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b733/9891439/045c93f3d3da/bs9-5-25-g001.jpg

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