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重组粒细胞-巨噬细胞集落刺激因子对小鼠体内外血小板生成的影响。

Effect of recombinant granulocyte-macrophage colony-stimulating factor on murine thrombocytopoiesis in vitro and in vivo.

作者信息

Ishibashi T, Kimura H, Shikama Y, Uchida T, Kariyone S, Maruyama Y

机构信息

First Department of Internal Medicine, Fukushima Medical College, Japan.

出版信息

Blood. 1990 Apr 1;75(7):1433-8.

PMID:2180495
Abstract

To investigate the effect of recombinant granulocyte-macrophage colony-stimulating factor (rGM-CSF) on murine megakaryocytopoiesis in vitro, the factor was added to both serum-free colony assays and liquid marrow cultures. GM-CSF had a significant megakaryocytic colony-stimulating activity. After 2 hours of preincubation with and without 10 ng/mL rGM-CSF, the percentage of megakaryocyte colony-forming cell (CFU-MK) in DNA synthesis was determined by tritiated-thymidine suicide using colony growth. The reduction of CFU-MK colony numbers in marrow culture was 47.5% +/- 9.9%, 20.9% +/- 5.2% (control), respectively, indicating that the factor affected cell cycle at CFU-MK levels. When acetylcholinesterase (AchE) production was measured fluorometrically after 4 days of liquid culture, rGM-CSF elicited an increase in AchE activity in a dose-dependent fashion. To determine if the hematopoietin acts directly on megakaryocytic differentiation, 2 ng/mL rGM-CSF was added to serum-free cultures of 295 single megakaryocytes isolated from CFU-MK colonies. An increase in size was observed in 65% of cells initially 10 to 20 microns in diameter, 71% of cells 20 to 30 microns, and 40% of cells greater than 30 microns. Conversely, in absence of GM-CSF, 17%, 31%, and 10% of cells in each group increased in diameter. These data suggest that rGM-CSF promotes murine megakaryocytopoiesis in vitro and that the response to the factor is direct. To determine if the factor influences megakaryocytic/thrombocytic lineage in vivo, 1 and 5 micrograms of rGM-CSF were administered intraperitoneally every 12 hours for 6 consecutive days. Although a two- to three-fold increase in peripheral granulocytes was observed, neither megakaryocytic progenitor cells or platelets changed. Histologic analysis of bone marrow megakaryocytes showed no increase in size and number. The in vivo studies demonstrated no effect of GM-CSF on thrombocytopoiesis. The discrepancies between the in vitro and in vivo effects of GM-CSF require additional investigations.

摘要

为研究重组粒细胞-巨噬细胞集落刺激因子(rGM-CSF)对体外小鼠巨核细胞生成的影响,将该因子添加至无血清集落测定和液体骨髓培养中。GM-CSF具有显著的巨核细胞集落刺激活性。在有和无10 ng/mL rGM-CSF的情况下预孵育2小时后,通过使用集落生长的氚化胸腺嘧啶自杀法测定巨核细胞集落形成细胞(CFU-MK)在DNA合成中的百分比。骨髓培养中CFU-MK集落数量的减少分别为47.5%±9.9%、20.9%±5.2%(对照),表明该因子在CFU-MK水平影响细胞周期。在液体培养4天后通过荧光法测量乙酰胆碱酯酶(AchE)产生时,rGM-CSF以剂量依赖性方式引起AchE活性增加。为确定造血因子是否直接作用于巨核细胞分化,将2 ng/mL rGM-CSF添加至从CFU-MK集落分离的295个单个巨核细胞的无血清培养物中。观察到初始直径为10至20微米的细胞中有65%、20至30微米的细胞中有71%以及大于30微米的细胞中有40%的细胞大小增加。相反,在无GM-CSF的情况下,每组中17%、31%和10%的细胞直径增加。这些数据表明rGM-CSF在体外促进小鼠巨核细胞生成,并且对该因子的反应是直接的。为确定该因子在体内是否影响巨核细胞/血小板谱系,连续6天每12小时腹腔注射1和5微克rGM-CSF。尽管观察到外周粒细胞增加了两到三倍,但巨核细胞祖细胞或血小板均未改变。骨髓巨核细胞的组织学分析显示大小和数量均未增加。体内研究表明GM-CSF对血小板生成无影响。GM-CSF体外和体内作用之间的差异需要进一步研究。

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