Kimura A, Katoh O, Kuramoto A
Department of Internal Medicine, Hiroshima University, Japan.
Br J Haematol. 1988 May;69(1):9-12. doi: 10.1111/j.1365-2141.1988.tb07595.x.
The effects of three growth factors contained in platelets on human bone marrow fibroblasts as well as fibroblast colony-forming cells were investigated to clarify the pathogenesis of marrow fibrosis frequently associated with myeloproliferative disorders. Two growth factors, platelet derived growth factor (PDGF) and epidermal growth factor (EGF), cooperatively stimulated the growth of passaged fibroblasts as well as fibroblast colony-forming cells. Transforming growth factor-beta augmented the growth of fibroblasts at low concentrations in the presence of EGF and/or PDGF, but inhibited that of colony-forming cells in the presence of PDGF or EGF. These results suggest that the growth of fibroblasts causing marrow fibrosis might be finely regulated, depending on the concentrations of growth factors released or leaked from platelets or megakaryocytes into marrow environment.
研究了血小板中所含三种生长因子对人骨髓成纤维细胞以及成纤维细胞集落形成细胞的作用,以阐明骨髓纤维化的发病机制,骨髓纤维化常与骨髓增殖性疾病相关。两种生长因子,血小板衍生生长因子(PDGF)和表皮生长因子(EGF),协同刺激传代成纤维细胞以及成纤维细胞集落形成细胞的生长。在EGF和/或PDGF存在的情况下,转化生长因子-β在低浓度时增强成纤维细胞的生长,但在PDGF或EGF存在时抑制集落形成细胞的生长。这些结果表明,导致骨髓纤维化的成纤维细胞的生长可能受到精细调节,这取决于从血小板或巨核细胞释放或泄漏到骨髓环境中的生长因子的浓度。