Suppr超能文献

在造血干细胞系和多能祖细胞上鉴定出一种独特的膜结合分子。

Identification of a unique membrane-bound molecule on a hemopoietic stem cell line and on multipotent progenitor cells.

作者信息

Han X D, Chung S W, Wong P M

机构信息

Fels Institute for Cancer Research and Molecular Biology, Department of Pathology and Lab Medicine, Temple University, Philadelphia, PA 19140, USA.

出版信息

Proc Natl Acad Sci U S A. 1995 Nov 21;92(24):11014-8. doi: 10.1073/pnas.92.24.11014.

Abstract

Hemopoietic stem cells are a distinct population of cells that can differentiate into multilineages of hemopoietic cells and have long-term repopulation capability. A few membrane-bound molecules have been found to be preferentially, but not uniquely, present on the surface of these primitive cells. We report here the identification of a unique 105-kDa glycoprotein on the surface of hemopoietic stem cell line BL3. This molecule, recognized by the absorbed antiserum, is not present on the surface of myeloid progenitors 32D and FDC-P1 cells, EL4 T cells, and NIH 3T3 fibroblasts. This antiserum can also be used to block the proliferation of BL3 cells even in the presence of mitogen-stimulated spleen cell conditioned medium, which is known to have a stimulating activity on BL3 cells. It can also inhibit development of in vitro, fetal liver cell-derived multilineage colonies, but not other types of colonies, and of in vivo bone marrow cell-derived colony-forming unit spleen foci. These data suggest that gp105 plays an important role in hemopoietic stem cell differentiation.

摘要

造血干细胞是一类独特的细胞群体,能够分化为多种造血细胞谱系,并具有长期重建能力。已发现一些膜结合分子优先(但并非唯一)存在于这些原始细胞的表面。我们在此报告在造血干细胞系BL3表面鉴定出一种独特的105 kDa糖蛋白。这种分子可被吸收抗血清识别,不存在于髓系祖细胞32D和FDC-P1细胞、EL4 T细胞及NIH 3T3成纤维细胞的表面。这种抗血清还可用于阻断BL3细胞的增殖,即使在存在有丝分裂原刺激的脾细胞条件培养基的情况下也是如此,已知该条件培养基对BL3细胞具有刺激活性。它还能抑制体外胎儿肝细胞来源的多谱系集落的形成,但不影响其他类型集落的形成,以及体内骨髓细胞来源的集落形成单位脾灶的形成。这些数据表明gp105在造血干细胞分化中起重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc8c/40561/fd10f7c197e0/pnas01502-0207-a.jpg

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