Felix R, Elford P R, Stoercklé C, Cecchini M, Wetterwald A, Trechsel U, Fleisch H, Stadler B M
Department of Pathophysiology, University of Berne, Switzerland.
J Bone Miner Res. 1988 Feb;3(1):27-36. doi: 10.1002/jbmr.5650030106.
This study was carried out to determine whether bone might be a source of hemopoietic growth factors. Both neonatal murine calvaria and primary cultures of cells isolated from calvaria released, upon stimulation with lipopolysaccharide, an activity that stimulated the growth of the interleukin (IL) 3-dependent cell lines, 32D cl, 123, and NSF 60. Upon gel filtration, this activity eluted with a molecular weight of 30,000 kDa. Further characterization, however, revealed that the major activity in conditioned medium was not IL 3. Activity was absorbed by DEAE-Sephacel at low salt concentration, whereas IL 3 does not adhere. Furthermore, an IL 3-specific antiserum did not neutralize the activity from cells and only partly neutralized the activity generated by whole calvaria. After gel filtration, the 30-kDa activity stimulated the growth of very large colonies in semisolid medium consisting mainly of granulocytes with the remainder being macrophages. No colony types belonging to other hemopoietic lineages were found, indicating, again, that the activity was not identical to IL 3. Subsequently, conditioned medium was fractionated by hydrophobic chromatography on Phenyl-Sepharose CL-4B, yielding two peaks of activity. Neutralization of activity with antisera to granulocyte-macrophage colony-stimulating factor (GM-CSF) and IL 3 and use of colony assays showed that medium conditioned by whole calvaria contained GM-CSF and granulocyte CSF (G-CSF) in similar amounts together with a little IL 3, and medium conditioned with calvaria cells contained GM-CSF and little G-CSF. We conclude that bone releases hemopoietic growth factors that could contribute both to hemopoiesis and to the recruitment of osteoclasts from progenitors resident in the adjacent marrow.
本研究旨在确定骨骼是否可能是造血生长因子的来源。新生小鼠颅骨以及从颅骨分离的原代细胞培养物在受到脂多糖刺激后,均释放出一种活性物质,该活性物质可刺激白细胞介素(IL)3依赖的细胞系32D cl、123和NSF 60的生长。经凝胶过滤,该活性物质以30,000 kDa的分子量洗脱。然而,进一步的表征显示,条件培养基中的主要活性物质并非IL 3。该活性物质在低盐浓度下被DEAE-葡聚糖凝胶吸附,而IL 3并不吸附。此外,IL 3特异性抗血清不能中和细胞产生的活性,只能部分中和完整颅骨产生的活性。凝胶过滤后,30 kDa的活性物质在主要由粒细胞组成、其余为巨噬细胞的半固体培养基中刺激形成非常大的集落。未发现属于其他造血谱系的集落类型,这再次表明该活性物质与IL 3不同。随后,通过在苯基-葡聚糖凝胶CL-4B上进行疏水层析对条件培养基进行分级分离,得到两个活性峰。用粒细胞-巨噬细胞集落刺激因子(GM-CSF)和IL 3的抗血清中和活性并进行集落测定表明,完整颅骨条件培养基中GM-CSF和粒细胞集落刺激因子(G-CSF)的含量相似,同时含有少量IL 3,而颅骨细胞条件培养基中含有GM-CSF和少量G-CSF。我们得出结论,骨骼释放的造血生长因子可能有助于造血以及从邻近骨髓中的祖细胞招募破骨细胞。