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体外定量分析多谱系造血集落形成细胞的前体细胞(前CFC多能)。白细胞介素-1需求的独特性、与多能集落形成细胞的部分分离以及与体内长期重建细胞的相关性。

Precursors (pre-CFCmulti) of multilineage hemopoietic colony-forming cells quantitated in vitro. Uniqueness of IL-1 requirement, partial separation from pluripotential colony-forming cells, and correlation with long term reconstituting cells in vivo.

作者信息

Iscove N N, Yan X Q

机构信息

Ontario Cancer Institute, Toronto, Canada.

出版信息

J Immunol. 1990 Jul 1;145(1):190-5.

PMID:2358672
Abstract

Pluripotential colony-forming cells (CFCmulti) from mouse marrow can expand significantly in number during 4 days of suspension culture with IL-1 and IL-3. In this study, the cells ("pre-CFCmulti") which originate this response are characterized in terms of their frequency, progeny number, factor requirements, buoyant density, and extent of restoration following marrow transplantation. Parallel measurements of both CFCmulti and cells providing long term marrow reconstitution in vivo allowed direct comparisons to be made with pre-CFCmulti. The proliferative response of pre-CFCmulti was found to depend uniquely on the combination of IL-1 and IL-3, and neither of these regulators was replaceable by any of IL-4, IL-6, IL-7, GM-CSF, G-CSF, M-CSF or LIF. After separation on density gradients, pre-CFCmulti were recovered in fractions of lower density than most of the CFCmulti, but in the same fractions that contained most of the in vivo reconstituting cells. After irradiation and marrow transplantation, marrow CFCmulti were restored to near normal levels, while both pre-CFCmulti as well as reconstituting stem cells remained profoundly depressed. These results show pre-CFCmulti to be distinct from most CFCmulti and to represent the closest approach to quantitative detection of reconstituting stem cells so far achieved in vitro.

摘要

来自小鼠骨髓的多能集落形成细胞(CFCmulti)在与白细胞介素-1(IL-1)和白细胞介素-3(IL-3)进行4天的悬浮培养期间,数量可显著增加。在本研究中,引发这种反应的细胞(“前CFCmulti”)在频率、子代数量、因子需求、浮力密度以及骨髓移植后的恢复程度等方面进行了特征描述。对CFCmulti和在体内提供长期骨髓重建的细胞进行平行测量,使得能够直接与前CFCmulti进行比较。发现前CFCmulti的增殖反应唯一地依赖于IL-1和IL-3的组合,并且这些调节因子中的任何一个都不能被IL-4、IL-6、IL-7、粒细胞-巨噬细胞集落刺激因子(GM-CSF)、粒细胞集落刺激因子(G-CSF)、巨噬细胞集落刺激因子(M-CSF)或白血病抑制因子(LIF)所替代。在密度梯度分离后,前CFCmulti在比大多数CFCmulti密度更低的组分中被回收,但与包含大多数体内重建细胞的组分相同。照射和骨髓移植后,骨髓CFCmulti恢复到接近正常水平,而前CFCmulti以及重建干细胞仍然严重减少。这些结果表明前CFCmulti与大多数CFCmulti不同,并且代表了迄今为止在体外实现的对重建干细胞进行定量检测的最接近方法。

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