Gordon M Y
Stem Cells (1981). 1982;1(3):180-92.
The functional relationships between bone marrow fibroblastoid cells, granulocyte-macrophage colony-forming cells (GM-CFC) and colony-stimulating factor (CSF) have been investigated in vitro. Cultured fibroblastoid cells neither produce CSF nor release a factor which increases the production of CSF by plastic-adherent colony-stimulating cells (CSC). However, the presence of fibroblastoid cells in agar cultures containing performed CSF increases the plating efficiency of GM-CFC. The fibroblastoid cells seem to act either by increasing the stimulatory activity of CSF or by releasing a stimulatory factor in the presence of CSF. The sensitivity of the colony-forming cells to CSF was not modified by contact with the fibroblastoid stromal cells. Fibroblastoid cells themselves were required for demonstration of the enhancement of CSF since the effect could not be reproduced using supernatant medium from fibroblast cultures. Different effects were seen when supernatant media from fibroblastoid cultures were incorporated into agar cultures of GM-CFC or into liquid cultures of bone marrow cells. The culture supernatants contain soluble factors which inhibit the formation of granulocyte-macrophage colonies in CSF-stimulated agar cultures and activities which increase the survival of GM-CFC in liquid cultures. The results suggest that stable long-range and transient short-range influences of bone marrow fibroblastoid cells may be involved in the regulation of granulopoiesis.
已在体外研究了骨髓成纤维样细胞、粒细胞-巨噬细胞集落形成细胞(GM-CFC)与集落刺激因子(CSF)之间的功能关系。培养的成纤维样细胞既不产生CSF,也不释放可增加塑料贴壁集落刺激细胞(CSC)产生CSF的因子。然而,在含有预先形成的CSF的琼脂培养物中,成纤维样细胞的存在可提高GM-CFC的接种效率。成纤维样细胞似乎通过增强CSF的刺激活性或在CSF存在时释放刺激因子来发挥作用。集落形成细胞对CSF的敏感性不会因与成纤维样基质细胞接触而改变。由于使用成纤维细胞培养物的上清培养基无法重现这种效应,因此需要成纤维样细胞本身来证明CSF的增强作用。当将成纤维样培养物的上清培养基加入GM-CFC的琼脂培养物或骨髓细胞的液体培养物中时,会观察到不同的效果。培养上清液含有可抑制CSF刺激的琼脂培养物中粒细胞-巨噬细胞集落形成的可溶性因子,以及可增加液体培养物中GM-CFC存活率的活性物质。结果表明,骨髓成纤维样细胞的稳定的长程和短暂的短程影响可能参与粒细胞生成的调节。