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单克隆抗体J11d.2可识别处于细胞周期休眠状态的小鼠原始造血祖细胞。

Monoclonal antibody J11d.2 recognizes cell cycle-dormant, primitive hematopoietic progenitors of mice.

作者信息

Shih J P, Ogawa M

机构信息

Department of Medicine, Medical University of South Carolina, Charleston.

出版信息

Blood. 1993 Mar 1;81(5):1155-60.

PMID:8443377
Abstract

It was reported that monoclonal antibody (MoAb) J11d.2 reacts with mature blood cells of mice but not with their progenitors. We tested in culture studies whether this antibody could be used for enrichment for primitive marrow progenitors. The majority of colony-forming cells including multipotential progenitors in the marrow cells from 5-fluorouracil (5-FU)-treated mice were J11d.2+, whereas most of the progenitors from normal mice were J11d.2-. In addition, formation of multilineage colonies from J11d.2+ in both 5-FU-treated and normal mice was augmented by interleukin 6. These observations indicated that MoAb J11d.2 recognizes cell cycle-dormant progenitors. We have recently described a simple method that provides 800-fold enrichment for the progenitors in post-5-FU marrow cells using MoAb D7 (anti-Ly-6A/E). When this method was modified to include sorting with MoAb J11d.2, D7+ J11d.2+ cells were 2,250-fold enriched for multipotential progenitors. Micromanipulation and culture of individual D7+ J11d.2+ cells showed that average plating efficiency of the cell population is approximately 70% and that about 30% of the progenitors are lymphohematopoietic in nature. These data demonstrate that J11d.2 is a useful MoAb for the isolation of primitive hematopoietic progenitors of mice.

摘要

据报道,单克隆抗体(MoAb)J11d.2与小鼠成熟血细胞反应,但不与其祖细胞反应。我们在培养研究中测试了该抗体是否可用于富集原始骨髓祖细胞。5-氟尿嘧啶(5-FU)处理的小鼠骨髓细胞中的大多数集落形成细胞,包括多能祖细胞,都是J11d.2阳性,而正常小鼠的大多数祖细胞是J11d.2阴性。此外,在5-FU处理的小鼠和正常小鼠中,J11d.2阳性细胞形成多谱系集落的能力都因白细胞介素6而增强。这些观察结果表明,MoAb J11d.2识别细胞周期静止的祖细胞。我们最近描述了一种简单的方法,使用MoAb D7(抗Ly-6A/E)可使5-FU处理后的骨髓细胞中的祖细胞富集800倍。当该方法修改为包括用MoAb J11d.2进行分选时,D7+ J11d.2+细胞中多能祖细胞的富集倍数达到2250倍。对单个D7+ J11d.2+细胞进行显微操作和培养表明,该细胞群体的平均接种效率约为70%,并且约30%的祖细胞本质上是淋巴细胞造血的。这些数据表明,J11d.2是分离小鼠原始造血祖细胞的一种有用的单克隆抗体。

相似文献

1
Monoclonal antibody J11d.2 recognizes cell cycle-dormant, primitive hematopoietic progenitors of mice.单克隆抗体J11d.2可识别处于细胞周期休眠状态的小鼠原始造血祖细胞。
Blood. 1993 Mar 1;81(5):1155-60.
2
Enrichment for primitive hemopoietic progenitors of marrow cells from 5-fluorouracil-treated mice and normal mice.
Blood Cells. 1994;20(1):7-11; discussion 11-3.
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Enrichment of murine marrow cells for progenitors of multilineage hemopoietic colonies.
Leukemia. 1992 Mar;6(3):193-8.
4
Thrombopoietin, the ligand for the Mpl receptor, synergizes with steel factor and other early acting cytokines in supporting proliferation of primitive hematopoietic progenitors of mice.血小板生成素,即Mpl受体的配体,可与干细胞因子及其他早期起作用的细胞因子协同作用,以支持小鼠原始造血祖细胞的增殖。
Blood. 1996 Jun 1;87(11):4544-51.
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Growth factor requirement for survival in cell-cycle dormancy of primitive murine lymphohematopoietic progenitors.
Blood. 1993 Feb 1;81(3):610-6.
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Monoclonal antibody LR-1 recognizes murine heat-stable antigen, a marker of antigen-presenting cells and developing hematopoietic cells.单克隆抗体LR-1可识别小鼠热稳定抗原,这是一种抗原呈递细胞和发育中的造血细胞的标志物。
Int Arch Allergy Immunol. 1996 Nov;111(3):218-29. doi: 10.1159/000237371.
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Isolation of primitive human bone marrow hematopoietic progenitor cells using Hoechst 33342 and Rhodamine 123.使用Hoechst 33342和罗丹明123分离原始人类骨髓造血祖细胞。
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CD43 expression by murine lymphohemopoietic progenitors.小鼠淋巴造血祖细胞的CD43表达
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The monoclonal antibody 97A6 defines a novel surface antigen expressed on human basophils and their multipotent and unipotent progenitors.单克隆抗体97A6可识别一种在人类嗜碱性粒细胞及其多能和单能祖细胞上表达的新型表面抗原。
Blood. 1999 Oct 1;94(7):2343-56.
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Purified primitive human hematopoietic progenitor cells with long-term in vitro repopulating capacity adhere selectively to irradiated bone marrow stroma.具有长期体外再增殖能力的纯化原始人类造血祖细胞选择性地黏附于经辐照的骨髓基质。
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引用本文的文献

1
Purified hematopoietic stem cells without facilitating cells can repopulate fully allogeneic recipients across entire major histocompatibility complex transplantation barrier in mice.不含辅助细胞的纯化造血干细胞能够跨越小鼠整个主要组织相容性复合体移植屏障,完全重建异基因受体。
Proc Natl Acad Sci U S A. 1997 Dec 23;94(26):14632-6. doi: 10.1073/pnas.94.26.14632.