首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Identification of a unique membrane-bound molecule on a hemopoietic stem cell line and on multipotent progenitor cells.
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Identification of a unique membrane-bound molecule on a hemopoietic stem cell line and on multipotent progenitor cells.

机译:鉴定造血干细胞系和多能祖细胞上独特的膜结合分子。

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摘要

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.
机译:造血干细胞是一个独特的细胞群,可以分化为造血细胞的多系,并具有长期的繁殖能力。已经发现一些膜结合分子优先但并非唯一地存在于这些原始细胞的表面。我们在这里报告造血干细胞系BL3表面独特的105 kDa糖蛋白的鉴定。被吸收的抗血清识别的该分子不存在于骨髓祖细胞32D和FDC-P1细胞,EL4 T细胞和NIH 3T3成纤维细胞的表面。即使在已知有丝分裂原刺激的脾细胞条件培养基的情况下,该抗血清也可用于阻断BL3细胞的增殖,已知该条件培养基对BL3细胞具有刺激活性。它还可以抑制体外胎儿肝细胞衍生的多谱系集落,但不能抑制其他类型的集落,以及体内骨髓细胞衍生的集落形成单位脾灶的发展。这些数据表明gp105在造血干细胞分化中起重要作用。

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