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与人类细小病毒B19感染相关的骨髓巨原红细胞中p53和Ki-67抗原的表达

Expression of p53 and Ki-67 antigen in bone marrow giant proerythroblasts associated with human parvovirus B19 infection.

作者信息

Sadahira Y, Sugihara T, Yawata Y

机构信息

Department of Pathology, Kawasaki Medical School, Kurashiki, Japan.

出版信息

Int J Hematol. 2001 Aug;74(2):147-52. doi: 10.1007/BF02981997.

Abstract

Giant proerythroblasts are hallmarks of human parvovirus B19 infection. We attempted to characterize these cells in 5 patients with parvovirus B19-induced pure red cell aplasia using immunostaining of paraffin-embedded bone marrow sections with antibodies against erythroid-lineage-specific proteins, viral capsid antigen VP-1, and apoptosis- and cell-cycle-related proteins. Giant proerythroblasts are immunohistochemically consistent with early erythroid precursors of cells in the differentiation stage of CD34-, cytoplasmic spectrin+, glycophorin A-, and band-3-. VP-1 was expressed in the nucleus and cytoplasm of small- to medium-sized spectrin+ erythroid cells but not in giant proerythroblasts. The giant proerythroblasts displayed nuclear staining for p53 (41%+/-16%) and Ki-67 antigen (100%+/-0%) and cytoplasmic staining for Bax (65%+/-11%) and procaspase-3 (78%+/-10%), whereas they were not stained for p21Wafl/Cip1, active form of caspase-3, or terminal deoxynucleotidyltransferase-mediated deoxyuridine nick-end labeling (TUNEL). Antiapoptotic proteins, Bcl-2 and Mcl-1, were not expressed in the giant cells, and Bcl-x was infrequently expressed in these cells (11%+/-4%). These immunohistochemical findings suggest that giant proerythroblasts are proliferating erythroid precursors with accumulation of nonfunctional p53.

摘要

巨大原始红细胞是人类细小病毒B19感染的标志。我们试图通过对5例细小病毒B19诱导的纯红细胞再生障碍性贫血患者石蜡包埋骨髓切片进行免疫染色,使用针对红系特异性蛋白、病毒衣壳抗原VP-1以及凋亡和细胞周期相关蛋白的抗体,来对这些细胞进行特征描述。巨大原始红细胞在免疫组织化学上与处于CD34-、细胞质血影蛋白+、血型糖蛋白A-和带3-分化阶段的细胞早期红系前体一致。VP-1在小到中等大小的血影蛋白+红系细胞的细胞核和细胞质中表达,但在巨大原始红细胞中不表达。巨大原始红细胞显示p53核染色(41%±16%)和Ki-67抗原核染色(100%±0%),Bax细胞质染色(65%±11%)和procaspase-3细胞质染色(78%±10%),而它们对p21Wafl/Cip1、活化形式的caspase-3或末端脱氧核苷酸转移酶介导的脱氧尿苷缺口末端标记(TUNEL)不染色。抗凋亡蛋白Bcl-2和Mcl-1在巨大细胞中不表达,Bcl-x在这些细胞中很少表达(11%±4%)。这些免疫组织化学结果表明,巨大原始红细胞是具有无功能p53积累的增殖性红系前体。

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