• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

照射后负责骨髓造血干细胞区室重建的原始细胞中CFU-S的分离:前CFU-S细胞的证据。

Separation of CFU-S from primitive cells responsible for reconstitution of the bone marrow hemopoietic stem cell compartment following irradiation: evidence for a pre-CFU-S cell.

作者信息

Ploemacher R E, Brons R H

机构信息

Department of Cell Biology and Genetics, Erasmus University, Rotterdam, The Netherlands.

出版信息

Exp Hematol. 1989 Mar;17(3):263-6.

PMID:2563690
Abstract

We have studied the in vivo spleen colony-forming ability and marrow repopulating ability of murine bone marrow cells differing in mitochondrial activity. Following centrifugal elutriation the cells were sorted on the basis of rhodamine-123 fluorescence intensity within a predetermined light scatter window. It is shown that a class of hemopoietic stem cells exists that differs from the majority of day-12 spleen colony-forming units (CFU-S) in that it has low mitochondrial activity and a high capacity to generate in time new day-12 CFU-S and cells that rescue recipients from radiation-inflicted death. These data add direct evidence for the identity of pre-CFU-S and CFU-S by physical separation.

摘要

我们研究了线粒体活性不同的小鼠骨髓细胞的体内脾集落形成能力和骨髓重建能力。通过离心淘洗后,在预定的光散射窗口内,根据罗丹明-123荧光强度对细胞进行分选。结果表明,存在一类造血干细胞,它与大多数第12天的脾集落形成单位(CFU-S)不同,其线粒体活性低,能够及时产生新的第12天CFU-S以及能使受辐照受体免于死亡的细胞。这些数据通过物理分离为前CFU-S和CFU-S的一致性提供了直接证据。

相似文献

1
Separation of CFU-S from primitive cells responsible for reconstitution of the bone marrow hemopoietic stem cell compartment following irradiation: evidence for a pre-CFU-S cell.照射后负责骨髓造血干细胞区室重建的原始细胞中CFU-S的分离:前CFU-S细胞的证据。
Exp Hematol. 1989 Mar;17(3):263-6.
2
Isolation of hemopoietic stem cell subsets from murine bone marrow: II. Evidence for an early precursor of day-12 CFU-S and cells associated with radioprotective ability.从小鼠骨髓中分离造血干细胞亚群:II. 12日CFU-S早期前体及与辐射防护能力相关细胞的证据。
Exp Hematol. 1988 Jan;16(1):27-32.
3
Multiparameter analysis of transplantable hemopoietic stem cells. II. Stem cells of long-term bone marrow-reconstituted recipients.可移植造血干细胞的多参数分析。II. 长期骨髓重建受体的干细胞
Exp Hematol. 1988 May;16(4):245-9.
4
Isolation of hemopoietic stem cell subsets from murine bone marrow: I. Radioprotective ability of purified cell suspensions differing in the proportion of day-7 and day-12 CFU-S.从小鼠骨髓中分离造血干细胞亚群:I. 不同第7天和第12天脾集落形成单位(CFU-S)比例的纯化细胞悬液的辐射防护能力
Exp Hematol. 1988 Jan;16(1):21-6.
5
Bulk enrichment of transplantable hemopoietic stem cell subsets from lipopolysaccharide-stimulated murine spleen.
Exp Hematol. 1987 Feb;15(2):154-62.
6
Rescue from lethal irradiation correlates with transplantation of 10-20 CFU-S-day 12.从致死性辐射中获救与第12天移植10 - 20个脾集落形成单位(CFU-S)相关。
Blood Cells Mol Dis. 1997 Aug;23(2):157-68. doi: 10.1006/bcmd.1997.0133.
7
Cells with marrow and spleen repopulating ability and forming spleen colonies on day 16, 12, and 8 are sequentially ordered on the basis of increasing rhodamine 123 retention.具有骨髓和脾脏重建能力且在第16天、12天和8天形成脾脏集落的细胞,根据罗丹明123保留量的增加依次排序。
J Cell Physiol. 1988 Sep;136(3):531-6. doi: 10.1002/jcp.1041360320.
8
Separation and functional analysis of bone marrow cells separated by rhodamine-123 fluorescence.通过罗丹明-123荧光分离的骨髓细胞的分离及功能分析
Exp Hematol. 1987 Jan;15(1):99-104.
9
Marrow repopulating cells, but not CFU-S, establish long-term in vitro hemopoiesis on a marrow-derived stromal layer.骨髓再植细胞而非脾集落形成单位(CFU-S),在源自骨髓的基质层上建立长期体外造血。
Exp Hematol. 1990 Sep;18(8):893-6.
10
Multiparameter analysis of transplantable hemopoietic stem cells: I. The separation and enrichment of stem cells homing to marrow and spleen on the basis of rhodamine-123 fluorescence.可移植造血干细胞的多参数分析:I. 基于罗丹明-123荧光对归巢至骨髓和脾脏的干细胞进行分离和富集。
Exp Hematol. 1985 Nov;13(10):999-1006.

引用本文的文献

1
The imprinted gene Pw1/Peg3 regulates skeletal muscle growth, satellite cell metabolic state, and self-renewal.印迹基因 Pw1/Peg3 调控骨骼肌生长、卫星细胞代谢状态和自我更新。
Sci Rep. 2018 Oct 2;8(1):14649. doi: 10.1038/s41598-018-32941-x.
2
Developmental changes in hematopoietic stem cell properties.造血干细胞特性的发育变化。
Exp Mol Med. 2013 Nov 15;45(11):e55. doi: 10.1038/emm.2013.98.
3
The Culture-Repopulating Ability assays and incubation in low oxygen: a simple way to test drugs on leukaemia stem or progenitor cells.
培养重建造能力测定法和低氧孵育:在白血病干细胞或祖细胞上测试药物的简单方法。
Curr Pharm Des. 2013;19(30):5374-83. doi: 10.2174/1381612811319300006.
4
Hematopoietic stem cells in research and clinical applications: The "CD34 issue".在研究和临床应用中的造血干细胞:“CD34 问题”。
World J Stem Cells. 2010 Apr 26;2(2):18-23. doi: 10.4252/wjsc.v2.i2.18.
5
Runx1 isoforms show differential expression patterns during hematopoietic development but have similar functional effects in adult hematopoietic stem cells.Runx1 异构体在造血发育过程中表现出不同的表达模式,但在成年造血干细胞中具有相似的功能效应。
Exp Hematol. 2010 May;38(5):403-16. doi: 10.1016/j.exphem.2010.02.011. Epub 2010 Mar 3.
6
Consistent, persistent expression from modified retroviral vectors in murine hematopoietic stem cells.经修饰的逆转录病毒载体在小鼠造血干细胞中持续、稳定的表达。
Proc Natl Acad Sci U S A. 1998 Aug 18;95(17):10182-7. doi: 10.1073/pnas.95.17.10182.
7
Alternative testing systems for evaluating noncarcinogenic, hematologic toxicity.用于评估非致癌性血液毒性的替代测试系统。
Environ Health Perspect. 1998 Apr;106 Suppl 2(Suppl 2):541-57. doi: 10.1289/ehp.98106541.
8
Murine natural killer cell differentiation: past, present, and future.小鼠自然杀伤细胞的分化:过去、现在与未来。
Immunol Res. 1996;15(2):151-62. doi: 10.1007/BF02918504.
9
Isolation and functional properties of murine hematopoietic stem cells that are replicating in vivo.体内正在进行复制的小鼠造血干细胞的分离及其功能特性
J Exp Med. 1996 Apr 1;183(4):1797-806. doi: 10.1084/jem.183.4.1797.
10
Identification and characterization of hematopoietic stem cells from the yolk sac of the early mouse embryo.早期小鼠胚胎卵黄囊中造血干细胞的鉴定与特性分析。
Proc Natl Acad Sci U S A. 1993 Nov 1;90(21):10110-4. doi: 10.1073/pnas.90.21.10110.