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成纤维细胞生长因子9对小鼠血小板生成的刺激作用。

Stimulation of thrombopoiesis in mice by fibroblast growth factor 9.

作者信息

Matsumoto-Yoshitomi S, Seko C, Kuroshima K, Naruo K, Shino A, Kondo T, Kurokawa T

机构信息

Department II, Takeda Chemical Industries Ltd, Osaka, Japan.

出版信息

Growth Factors. 1995;12(3):179-90. doi: 10.3109/08977199509036878.

Abstract

Fibroblast growth factor 9 (FGF-9), a novel member of the FGF family, was found to have thrombopoietic activity in vitro and in vivo. In an in vitro megakaryocyte colony-stimulating factor assay, anti-mouse interleukin-6 (IL-6) monoclonal antibody neutralized FGF-9 activity. This suggests that the activity may be exerted via IL-6 induction. BALB/c mice that received subcutaneous FGF-9 injections of 4 to 100 micrograms/day for 2 weeks showed a dose-dependent transient increase in peripheral platelet counts 10 to 12 days after the first treatment. Histologic studies showed a marked increase in megakaryocytes in bone marrow and extramedullary hematopoiesis in the spleen and the liver. Examination of changes in the DNA content of bone marrow megakaryocytes revealed that the ploidy distribution underwent a marked shift 3 days after FGF-9 injection, with a large increase in the 2N megakaryocyte population. The major modal ploidy shifted from the normal 16N to 2N. The number of megakaryocyte progenitor cells in FGF-9-treated mice increased up to 1.5-fold in the bone marrow and 10-fold in the spleen on day 6. These results indicate that FGF-9 acts on the in vivo proliferation of megakaryocytes.

摘要

成纤维细胞生长因子9(FGF-9)是FGF家族的一个新成员,已发现在体外和体内均具有促血小板生成活性。在体外巨核细胞集落刺激因子测定中,抗小鼠白细胞介素-6(IL-6)单克隆抗体可中和FGF-9的活性。这表明该活性可能是通过诱导IL-6发挥作用的。接受皮下注射FGF-9(4至100微克/天),持续2周的BALB/c小鼠在首次治疗后10至12天,外周血小板计数呈剂量依赖性短暂增加。组织学研究显示,骨髓中的巨核细胞以及脾脏和肝脏中的髓外造血均显著增加。对骨髓巨核细胞DNA含量变化的检查发现,FGF-9注射3天后,倍性分布发生了显著变化,2N巨核细胞群体大幅增加。主要的倍性模式从正常的16N转变为2N。在第6天,FGF-9处理小鼠的巨核细胞祖细胞数量在骨髓中增加至1.5倍,在脾脏中增加至10倍。这些结果表明,FGF-9作用于体内巨核细胞的增殖。

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