Characterization and induction of a cell line established from a patient with erythroleukemia (FAB M6).

H Kambayashi, M Kawaguchi, R Abe, H Kimura, S Kariyone
{"title":"Characterization and induction of a cell line established from a patient with erythroleukemia (FAB M6).","authors":"H Kambayashi,&nbsp;M Kawaguchi,&nbsp;R Abe,&nbsp;H Kimura,&nbsp;S Kariyone","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>A human cell line, designated as NISI, was established from a patient with erythroleukemia (FAB M6). The presence of a chromosome marker in NISI line indicates that it is derived from the leukemic clone which bears the common marker. The cell line shows morphology of immature erythroblast and has myelocytic properties from surface immunophenotyping. The differentiation capacities of NISI cells by three inducers (hemin, phorbor 12-myristate 13-acetate and 1-25-(OH)2D3) were evaluated. Hemin treated cells showed a significant increase in erythroid antigen expression as well as an increase in number of benzidine positive cells. Phorbor 12-myristate 13-acetate treated cells demonstrated a significant increase in megakaryocytic antigen expression, and a slightly diminished CD36 antigen expression. The surface markers of 1-25-(OH)2D3 treated cells did not demonstrate significant changes. NISI cell line, a human erythroleukemia cell line, still retained the tendency for differentiation to megakaryocytic lineage.</p>","PeriodicalId":76233,"journal":{"name":"Nihon Ketsueki Gakkai zasshi : journal of Japan Haematological Society","volume":"53 1","pages":"35-44"},"PeriodicalIF":0.0000,"publicationDate":"1990-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nihon Ketsueki Gakkai zasshi : journal of Japan Haematological Society","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

A human cell line, designated as NISI, was established from a patient with erythroleukemia (FAB M6). The presence of a chromosome marker in NISI line indicates that it is derived from the leukemic clone which bears the common marker. The cell line shows morphology of immature erythroblast and has myelocytic properties from surface immunophenotyping. The differentiation capacities of NISI cells by three inducers (hemin, phorbor 12-myristate 13-acetate and 1-25-(OH)2D3) were evaluated. Hemin treated cells showed a significant increase in erythroid antigen expression as well as an increase in number of benzidine positive cells. Phorbor 12-myristate 13-acetate treated cells demonstrated a significant increase in megakaryocytic antigen expression, and a slightly diminished CD36 antigen expression. The surface markers of 1-25-(OH)2D3 treated cells did not demonstrate significant changes. NISI cell line, a human erythroleukemia cell line, still retained the tendency for differentiation to megakaryocytic lineage.

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
红细胞白血病(FAB M6)患者细胞系的鉴定和诱导。
从一名红细胞白血病患者(FAB M6)身上建立了一株被命名为NISI的人细胞系。NISI系中染色体标记的存在表明它来源于具有共同标记的白血病克隆。细胞系表现为未成熟红母细胞形态,表面免疫表型分析显示具有髓细胞特性。研究了三种诱导剂(血红素、12-肉豆蔻酸酯13-乙酸磷和1-25-(OH)2D3)对NISI细胞分化能力的影响。Hemin处理后的细胞红细胞抗原表达显著增加,联苯胺阳性细胞数量显著增加。phoror 12-肉豆酸酯13-乙酸处理的细胞显示巨核细胞抗原表达显著增加,CD36抗原表达略有减少。1-25-(OH)2D3处理的细胞表面标志物无明显变化。NISI细胞系是一种人红白血病细胞系,仍然保持向巨核细胞谱系分化的趋势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
The hematopoietic system [Application of nucleolar organizer region staining technique to air-dried blood smears]. [Biochemical and molecular biological studies on beta-glucuronidase in myelogenous leukemic cells]. [Production and secretion of BSF2/IL6 in a case of hairy cell leukemia with polyclonal hypergammaglobulinemia]. [Long-term cultures of marrow cells from the patients with aplastic anemia].
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1