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γ干扰素主要对小鼠红系祖细胞发育的最早阶段发挥负调控作用。

Interferon-gamma exerts its negative regulatory effect primarily on the earliest stages of murine erythroid progenitor cell development.

作者信息

Wang C Q, Udupa K B, Lipschitz D A

机构信息

Geriatric Research Education and Clinical Center (GRECC), John L. McClellan Memorial Veterans Hospital, Little Rock, Arkansas 72205.

出版信息

J Cell Physiol. 1995 Jan;162(1):134-8. doi: 10.1002/jcp.1041620116.

Abstract

Interferon-gamma (INF-gamma) has been shown to suppress erythropoiesis and perhaps to contribute to the anemia of chronic disease. In this study we demonstrated that the concentration of INF gamma required to suppress murine burst forming unit-erythroid (BFU-E) growth was significantly less than that required to suppress colony forming unit-erythroid (CFU-E) growth. INF gamma acted at the most primitive step in erythroid progenitor cell differentiation and proliferation, as inhibition was maximal when added at the time of BFU-E culture initiation. Inhibition was progressively less if INF gamma addition was delayed after culture initiation. The effects of INF gamma on BFU-E did not require the presence of interleukin-1 alpha (IL-1 alpha), tumor necrosis factor-alpha (TNF alpha), or granulocyte macrophage colony stimulating factor (GM-CSF), as its effects were not neutralized by monoclonal antibodies against IL-1 alpha, TNF alpha, or GM-CSF. This applied whether INF gamma was added to culture with individual antibodies or with a combination of all three antibodies. INF gamma was not required for IL-1 alpha- or TNF alpha-induced suppression of BFU-E, as their effects were not neutralized by a monoclonal anti-INF gamma antibody. In contrast, GM-CSF-induced suppression of BFU-E was negated by the simultaneous addition of anti-INF gamma. We have previously shown that the addition of TNF alpha does not suppress BFU-E growth in cultures from marrow depleted of macrophages. Suppression did occur, however, if a small concentration of INF gamma that does not inhibit and increasing concentration of TNF alpha were added to culture, suggesting a synergistic effect between INF-gamma and TNF alpha. These observations suggest that INF gamma is a potent direct inhibitor of erythroid colony growth in vitro. It exerts its negative regulatory effect primarily on the earliest stages of erythroid progenitor cell differentiation and proliferation, as much higher doses are required to suppress late erythroid cell development. INF gamma is also involved in GM-CSF-induced inhibition of BFU-E colony growth.

摘要

γ干扰素(INF-γ)已被证明可抑制红细胞生成,可能与慢性病贫血有关。在本研究中,我们证明抑制小鼠红细胞爆式集落形成单位(BFU-E)生长所需的INF-γ浓度显著低于抑制红细胞集落形成单位(CFU-E)生长所需的浓度。INF-γ作用于红系祖细胞分化和增殖的最原始阶段,因为在BFU-E培养开始时添加时抑制作用最大。如果在培养开始后延迟添加INF-γ,抑制作用会逐渐减弱。INF-γ对BFU-E的作用不需要白细胞介素-1α(IL-1α)、肿瘤坏死因子-α(TNF-α)或粒细胞巨噬细胞集落刺激因子(GM-CSF)的存在,因为其作用不会被抗IL-1α、TNF-α或GM-CSF的单克隆抗体中和。无论INF-γ是与单个抗体还是与所有三种抗体的组合一起添加到培养物中,都是如此。IL-1α或TNF-α诱导的BFU-E抑制不需要INF-γ,因为它们的作用不会被抗INF-γ单克隆抗体中和。相反,同时添加抗INF-γ可消除GM-CSF诱导的BFU-E抑制。我们之前已经表明,添加TNF-α不会抑制来自巨噬细胞耗竭骨髓培养物中的BFU-E生长。然而,如果将不具有抑制作用的低浓度INF-γ和浓度不断增加的TNF-α添加到培养物中,抑制作用确实会发生,这表明INF-γ和TNF-α之间存在协同作用。这些观察结果表明,INF-γ是体外红系集落生长的有效直接抑制剂。它主要对红系祖细胞分化和增殖的最早阶段发挥负调节作用,因为抑制晚期红系细胞发育需要更高的剂量。INF-γ也参与GM-CSF诱导的BFU-E集落生长抑制。

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