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人粒细胞-巨噬细胞集落刺激因子(hGM-CSF)对hGM-CSF受体基因转基因小鼠分选的造血干细胞淋巴样和髓样分化的影响。

Effect of human granulocyte-macrophage colony stimulating factor (hGM-CSF) on lymphoid and myeloid differentiation of sorted hematopoietic stem cells from hGM-CSF receptor gene transgenic mice.

作者信息

Okubo T, Yanai N, Watanabe S, Arai K i, Obinata M

机构信息

Department of Cell Biology, Institute of Development, Aging and Cancer, Tohoku University, Sendai, 980-8575, Japan.

出版信息

J Biochem. 2000 Apr;127(4):591-6. doi: 10.1093/oxfordjournals.jbchem.a022645.

Abstract

Bone marrow lineage-negative (Lin(-)) c-Kit(+) Sca-1(+) hematopoietic cells from human GM-CSF receptor gene transgenic mice were cultured on established bone marrow stromal cell (TBR59) layers and on semisolid medium. In the semisolid assay, an increasing number of larger colonies were observed in the presence of hGM-CSF. By coculture with the stromal cells, cobblestones containing myeloid and lymphoid lineages of cells were formed from the stem cell enriched fraction, and addition of hGM-CSF strongly stimulated formation of the cobblestones containing both lineages. Repeating passages of the cobblestones on TBR59 stromal cells in the presence of hGM-CSF gradually decreased cobblestone formation and inversely increased macrophages and granulocytes, while mast cells were generated when the cells derived from the semisolid assay were cultured in a liquid medium containing hGM-CSF. These results consistently suggest that cytokines such as GM-CSF may costimulate the immature hematopoietic cells at their stroma-dependent phase before lineage commitment, and after commitment that occurs by an intrinsic program of the cells, they may stimulate maintenance and maturation of progenitor cells.

摘要

来自人GM-CSF受体基因转基因小鼠的骨髓谱系阴性(Lin(-))c-Kit(+) Sca-1(+)造血细胞,在已建立的骨髓基质细胞(TBR59)层和半固体培养基上培养。在半固体试验中,在hGM-CSF存在下观察到越来越多更大的集落。通过与基质细胞共培养,从富含干细胞的部分形成了包含髓系和淋巴系细胞的鹅卵石样结构,并且添加hGM-CSF强烈刺激了包含两个谱系的鹅卵石样结构的形成。在hGM-CSF存在下,在TBR59基质细胞上重复传代鹅卵石样结构逐渐减少了鹅卵石样结构的形成,反而增加了巨噬细胞和粒细胞,而当来自半固体试验的细胞在含有hGM-CSF的液体培养基中培养时则产生肥大细胞。这些结果一致表明,诸如GM-CSF之类的细胞因子可能在谱系定向之前的基质依赖阶段共刺激未成熟的造血细胞,并且在细胞通过其内在程序发生定向之后,它们可能刺激祖细胞的维持和成熟。

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