Caldwell J, Emerson S G
Department of Internal Medicine and Pediatrics, University of Michigan, Ann Arbor 48109.
J Cell Physiol. 1994 May;159(2):221-8. doi: 10.1002/jcp.1041590205.
Human bone marrow stromal cells respond to stimulation by the monokines IL-1 and TNF by producing colony-stimulating factors such as GM-CSF and G-CSF. In this study we show that IL-1 alpha and TNF alpha act synergistically to stimulate GM-CSF and G-CSF production by cultured marrow stromal cells. We further show that IL-1 alpha and TNF alpha synergistically stimulate production of GM-CSF and G-CSF by a clonal stroma-derived cell strain. Although IL-1 and TNF share many of the same biological activities, we show that IL-1 alpha and TNF alpha have an unequal ability to induce myeloid-CSF production by both cultures, with IL-1 alpha being the more potent inducer. We found that induction by IL-1 alpha and TNF alpha was independent of cell proliferation. The effect of IL-1 alpha and TNF alpha on production of the two myeloid-CSFs by the clonal cells was significantly greater than the unfractionated passaged stromal cultures, having the greater effect on G-CSF production. The clonally derived stromal cells constitutively produced colony-stimulating activity, in particular GM-CSF, at levels easily detected by ELISA. These findings show that, in addition to the overlapping and additive activities of IL-1 alpha and TNF alpha, they can interact synergistically. Our findings further suggest that a small subpopulation of stroma cells may be the major producer of G-CSF in the marrow microenvironment during immune response.
人骨髓基质细胞通过产生集落刺激因子如粒细胞-巨噬细胞集落刺激因子(GM-CSF)和粒细胞集落刺激因子(G-CSF)来响应单核因子白细胞介素-1(IL-1)和肿瘤坏死因子(TNF)的刺激。在本研究中,我们表明IL-1α和TNFα协同作用,刺激培养的骨髓基质细胞产生GM-CSF和G-CSF。我们进一步表明,IL-1α和TNFα协同刺激克隆的基质衍生细胞株产生GM-CSF和G-CSF。尽管IL-1和TNF具有许多相同的生物学活性,但我们表明IL-1α和TNFα诱导两种培养物产生髓系集落刺激因子的能力并不相同,其中IL-1α是更强效的诱导剂。我们发现IL-1α和TNFα的诱导作用与细胞增殖无关。IL-1α和TNFα对克隆细胞产生两种髓系集落刺激因子的影响明显大于未分级传代的基质培养物,对G-CSF产生的影响更大。克隆衍生的基质细胞组成性地产生集落刺激活性,特别是GM-CSF,其水平可通过酶联免疫吸附测定(ELISA)轻松检测到。这些发现表明,除了IL-1α和TNFα的重叠和累加活性外,它们还可以协同相互作用。我们的发现进一步表明,一小部分基质细胞可能是免疫反应期间骨髓微环境中G-CSF的主要产生者。