Majumdar M K, Thiede M A, Haynesworth S E, Bruder S P, Gerson S L
Osiris Therapeutics Inc., Baltimore, MD 21231, USA.
J Hematother Stem Cell Res. 2000 Dec;9(6):841-8. doi: 10.1089/152581600750062264.
Human mesenchymal stem cells (MSCs), bone marrow-derived pluripotent adherent cells of mesenchymal origin can differentiate along the osteogenic, chondrogenic, adipogenic, and tendonogenic lineages. In this report we characterize cytokine and growth factor gene expression by MSCs and investigate the modulation of cytokine expression that occurs during osteogenic and stromal differentiation. MSCs constitutively expressed mRNA for interleukin (IL)-6, IL-11, leukemia inhibitory factor (LIF), macrophage colony-stimulating factor (M-CSF), and stem cell factor (SCF). MSCs treated with IL-1alpha upregulated mRNA levels of IL-6, IL-11, and LIF, and began to express detectable levels of granulocyte colony-stimulating factor (G-CSF), granulocyte macrophage colony-stimulating factor (GM-CSF). mRNA levels of M-CSF and SCF did not change. MSCs cultured in osteogenic medium differentiated along the osteogenic lineage and downregulated mRNA levels of IL-6, IL-11 and LIF whereas, M-CSF and SCF expression were unchanged and G-CSF and GM-CSF remained undetectable. IL-3 was not detected in MSC culture under any conditions. MSCs precultured in control medium, IL-1alpha, or osteogenic medium maintained similar capacity to support long-term culture initiating cell (LT-CIC). Thus, primary and osteogenic differentiated MSCs produce important hematopoietic cytokines and support hematopoiesis in long-term cultures, suggesting that these cells may provide an excellent ex vivo environment for hematopoiesis during progenitor cell expansion and may be important for in vivo cell therapy.
人间充质干细胞(MSCs)是源自骨髓的多能间充质粘附细胞,可沿成骨、软骨生成、脂肪生成和肌腱生成谱系分化。在本报告中,我们对MSCs的细胞因子和生长因子基因表达进行了表征,并研究了成骨和基质分化过程中发生的细胞因子表达调节。MSCs组成性表达白细胞介素(IL)-6、IL-11、白血病抑制因子(LIF)、巨噬细胞集落刺激因子(M-CSF)和干细胞因子(SCF)的mRNA。用IL-1α处理的MSCs上调了IL-6、IL-11和LIF的mRNA水平,并开始表达可检测水平的粒细胞集落刺激因子(G-CSF)、粒细胞巨噬细胞集落刺激因子(GM-CSF)。M-CSF和SCF的mRNA水平没有变化。在成骨培养基中培养的MSCs沿成骨谱系分化,并下调了IL-6、IL-11和LIF的mRNA水平,而M-CSF和SCF的表达没有变化,G-CSF和GM-CSF仍无法检测到。在任何条件下,MSCs培养物中均未检测到IL-3。在对照培养基、IL-1α或成骨培养基中预培养的MSCs维持长期培养起始细胞(LT-CIC)的能力相似。因此,原代和成骨分化的MSCs产生重要的造血细胞因子,并在长期培养中支持造血,这表明这些细胞可能为祖细胞扩增期间的造血提供一个极好的体外环境,并且可能对体内细胞治疗很重要。