Barak V, Ben-Ishay Z
Department of Oncology, Hadassah University Hospital, Jerusalem, Israel.
Leuk Res. 1994 Oct;18(10):733-9. doi: 10.1016/0145-2126(94)90054-x.
A study of gene expression of GM-CSF, IL-3, c-kit ligand, and IL-1 by bone marrow stromal cells of mice who were treated with an LD50 cytosine arabinoside (Ara-C) dose was carried out. It was shown previously that this dose causes extensive hematopoietic damage which is followed by regeneration in surviving mice. Using PCR, we demonstrated GM-CSF and IL-1 expression by adherent cells taken from marrow fibroblast layers following Ara-C-induced hematopoietic damage and during marrow regeneration, while expression in control layers was not detected. The IL-3 gene was not expressed either by layers of Ara-C-treated mice or by controls, probably due to the absence of T-lymphocytes in 2-4 week old cultures. The c-kit ligand gene was expressed by layers during marrow regeneration and by control layers, but was absent during the stage of hematopoietic damage. In parallel, in vitro cytokine production was evaluated. While IL-3 and GM-CSF were not present in the conditioned medium of marrow fibroblast layers either from Ara-C-treated mice or controls, IL-1 was found in low concentrations in cultures from Ara-C-treated animals. We conclude that GM-CSF, c-kit ligand and IL-1 have important roles in sustaining marrow regeneration following extensive damage. The role of IL-3 in marrow regeneration cannot be assessed in fibroblast layers of 2-4 week incubation where T-lymphocytes are generally absent.
对接受半数致死量阿糖胞苷(Ara-C)治疗的小鼠骨髓基质细胞中GM-CSF、IL-3、c-kit配体和IL-1的基因表达进行了研究。先前已表明,该剂量会导致广泛的造血损伤,随后存活小鼠会出现再生。使用PCR,我们证明了在Ara-C诱导的造血损伤后及骨髓再生期间,从骨髓成纤维细胞层获取的贴壁细胞中存在GM-CSF和IL-1表达,而在对照层中未检测到表达。IL-3基因在Ara-C处理小鼠的细胞层和对照细胞层中均未表达,这可能是由于2 - 4周龄培养物中缺乏T淋巴细胞所致。c-kit配体基因在骨髓再生期间的细胞层和对照细胞层中均有表达,但在造血损伤阶段不存在。同时,对体外细胞因子产生进行了评估。在Ara-C处理小鼠或对照小鼠的骨髓成纤维细胞层的条件培养基中均未检测到IL-3和GM-CSF,但在Ara-C处理动物的培养物中发现了低浓度的IL-1。我们得出结论,GM-CSF、c-kit配体和IL-1在广泛损伤后的骨髓再生维持中具有重要作用。在通常缺乏T淋巴细胞的2 - 4周培养的成纤维细胞层中,无法评估IL-3在骨髓再生中的作用。