Kittler E L, McGrath H, Temeles D, Crittenden R B, Kister V K, Quesenberry P J
Department of Internal Medicine, University of Virginia Health Sciences Center, Charlottesville 22908.
Blood. 1992 Jun 15;79(12):3168-78.
The "stromal" or adherent cells of long-term murine Dexter explant bone marrow cultures provide the best in vitro model of the bone marrow microenvironment. Colony-stimulating factor-1 (CSF-1) is produced constitutively by these cells and is easily detected, but most investigators have not found constitutive production of the other hemolymphopoietic cytokines. We have previously reported the detection of granulocyte-macrophage-CSF (GM-CSF) in murine stromal cultures and its induction by the lectin Pokeweed mitogen. The present studies analyzing stromal cytokine messenger RNA (mRNA) production by standard Northern blot analysis show constitutive production of mRNAs for CSF-1, GM-CSF, granulocyte-CSF (G-CSF), c-kit ligand (KL), and interleukin-6 (IL-6), but not IL-3, IL-4, or IL-5 by 3-week irradiated or nonirradiated murine Dexter stromal cells. Exposure of stromal cells to Pokeweed mitogen or IL-1 16 hours before RNA harvest induces the messages for GM-CSF, G-CSF, KL, and IL-6, but not IL-3, IL-4, IL-5, or CSF-1. Polymerase chain reaction amplification of cDNA made with reverse transcriptase from stromal RNA using two separate sets of IL-3-specific primers shows the presence of IL-3 message in irradiated stromal cells, which is only detectable with this more sensitive technique. The factor-dependent cell lines FDC-P1 and 32D are supported by the stromal cells without the addition of exogenous growth factors, demonstrating a cytokine activity in these cultures that is inhibited by the addition of anti-IL-3 or anti-GM-CSF antibodies. These data indicate that murine Dexter stromal cells constitutively produce CSF-1, GM-CSF, G-CSF, IL-6, KL, and IL-3. This growth factor production could explain the support of granulocyte, macrophage, and megakaryocyte production and stem cell maintenance in Dexter-type long-term murine bone marrow cultures.
长期的小鼠德克斯特外植体骨髓培养中的“基质”或贴壁细胞提供了骨髓微环境的最佳体外模型。集落刺激因子-1(CSF-1)由这些细胞组成性产生且易于检测,但大多数研究者未发现其他造血细胞因子的组成性产生。我们之前报道过在小鼠基质培养物中检测到粒细胞-巨噬细胞集落刺激因子(GM-CSF)及其被凝集素商陆有丝分裂原诱导产生。目前通过标准Northern印迹分析对基质细胞因子信使核糖核酸(mRNA)产生情况进行的研究表明,3周龄经照射或未经照射的小鼠德克斯特基质细胞组成性产生CSF-1、GM-CSF、粒细胞集落刺激因子(G-CSF)、c-kit配体(KL)和白细胞介素-6(IL-6)的mRNA,但不产生IL-3、IL-4或IL-5的mRNA。在收获RNA前16小时将基质细胞暴露于商陆有丝分裂原或IL-1会诱导GM-CSF、G-CSF、KL和IL-6的信使,但不诱导IL-3、IL-4、IL-5或CSF-1的信使。使用两组不同的IL-3特异性引物对来自基质RNA经逆转录制成的cDNA进行聚合酶链反应扩增显示,经照射的基质细胞中存在IL-3信使,这只有通过这种更灵敏的技术才能检测到。依赖因子的细胞系FDC-P1和32D在不添加外源性生长因子的情况下得到基质细胞的支持,这表明这些培养物中存在一种细胞因子活性,该活性可被添加抗IL-3或抗GM-CSF抗体所抑制。这些数据表明,小鼠德克斯特基质细胞组成性产生CSF-1、GM-CSF、G-CSF、IL-6、KL和IL-3。这种生长因子的产生可以解释在德克斯特型长期小鼠骨髓培养中对粒细胞、巨噬细胞和巨核细胞产生以及干细胞维持的支持作用。