首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >A tumor necrosis factor-responsive long-term-culture-initiating cell is associated with the stromal layer of mouse long-term bone marrow cultures.
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A tumor necrosis factor-responsive long-term-culture-initiating cell is associated with the stromal layer of mouse long-term bone marrow cultures.

机译:肿瘤坏死因子响应的长期培养起始细胞与小鼠长期骨髓培养物的基质层有关。

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摘要

Long-term bone marrow cultures provide a model for the study of hematopoiesis. Both an intact, adherent stromal layer and hematopoietic stem cells are necessary components in these cultures. Mycophenolic acid treatment of mouse long-term bone marrow cultures depletes them of all assayable hematopoietic precursors. The residual stromal cells are functional and support hematopoiesis if new progenitor cells are supplied. We now show that these mycophenolic acid-treated stromal cell cultures contain cells capable of hematopoietic differentiation without the addition of new progenitors. When treated with tumor necrosis factor alpha (20-200 units/ml), the apparently pure stromal cultures undergo an intense burst of hematopoietic activity. After 4 days such cultures contain approximately 2 x 10(6) hematopoietic cells and, by 1 week, they are indistinguishable from control long-term cultures that were not treated with mycophenolic acid. These results suggest that the stromal cultures either contain hematopoietic stem cells that are maintained quiescent and mycophenolic acid-resistant, perhaps by intimate contact with the stroma, or contain adherent cells that can be induced to differentiate into hematopoietic stem cells. These stem cells are primitive, in that they are capable of multilineage development in the long-term cultures, but are unable to form spleen colonies or myeloid colonies in semisolid medium. These data demonstrate that the adherent fraction of cultured bone marrow contains very primitive hematopoietic cells and that tumor necrosis factor alpha activates their proliferation and differentiation. They also suggest a strategy for obtaining the earliest progenitors free of other, more mature cell types.
机译:长期骨髓培养为造血研究提供了模型。在这些培养物中,完整的粘附基质层和造血干细胞都是必需的成分。小鼠长期骨髓培养物中的麦考酚酸治疗可消除它们所有可测定的造血前体。如果提供了新的祖细胞,则残留的基质细胞将发挥功能并支持造血功能。现在我们显示,这些经过麦考酚酸处理的基质细胞培养物中包含的细胞能够进行造血分化,而无需添加新的祖细胞。当用肿瘤坏死因子α(20-200单位/毫升)治疗时,看似纯的基质培养物会经历强烈的造血活动。 4天后,此类培养物包含约2 x 10(6)的造血细胞,到1周时,它们与未经霉酚酸处理的对照长期培养物没有区别。这些结果表明,基质培养物要么包含可能通过与基质紧密接触而保持静止且对霉酚酸有抵抗力的造血干细胞,要么含有可以诱导分化为造血干细胞的贴壁细胞。这些干细胞是原始的,因为它们能够在长期培养中发展成多系,但不能在半固体培养基中形成脾集落或骨髓集落。这些数据表明,培养的骨髓的粘附部分含有非常原始的造血细胞,并且肿瘤坏死因子α激活了它们的增殖和分化。他们还提出了一种获得其他,更成熟细胞类型的最早祖细胞的策略。

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