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急性髓细胞白血病中原始祖细胞培养物中的贴壁细胞。

Adherent cells in cultures of blast progenitors in acute myeloblastic leukemia.

作者信息

Langley G R, Smith L J, McCulloch E A

出版信息

Leuk Res. 1986;10(8):953-9. doi: 10.1016/0145-2126(86)90248-1.

Abstract

Blast cells from patients with acute myelogenous leukemia (AML) grow exponentially in suspension culture and form colonies in cultures "stiffened" with methylcellulose; under both culture conditions, cells are generated which have the ability to adhere to plastic or glass. These adherent cells lack the capacity to form colonies, to proliferate in liquid culture or to support growth. Adherent cells are generated in parallel with changes in the frequency of clonogenic cells and express surface markers of AML blasts but with a higher frequency of an antigen recognized by the monoclonal MO1, a late stage marker associated with the macrophage differentiation lineage. While the appearance of adherent cells provides further evidence that blast cells follow differentiation programs in culture, the generation of adherent cells does not indicate that normal differentiation is occurring; rather the data is consistent with the view that components of normal monocytic differentiation programs are assembled abnormally in the programs of some blast progenitors.

摘要

急性髓性白血病(AML)患者的原始细胞在悬浮培养中呈指数生长,并在添加甲基纤维素而“硬化”的培养物中形成集落;在这两种培养条件下,都会产生能够粘附于塑料或玻璃的细胞。这些贴壁细胞缺乏形成集落、在液体培养中增殖或支持生长的能力。贴壁细胞与克隆形成细胞频率的变化同时产生,并表达AML原始细胞的表面标志物,但被单克隆抗体MO1识别的一种抗原频率更高,MO1是与巨噬细胞分化谱系相关的晚期标志物。虽然贴壁细胞的出现进一步证明原始细胞在培养中遵循分化程序,但贴壁细胞的产生并不表明正在发生正常分化;相反,数据与以下观点一致,即正常单核细胞分化程序的成分在一些原始祖细胞的程序中异常组装。

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