Rusten L S, Smeland E B, Jacobsen F W, Lien E, Lesslauer W, Loetscher H, Dubois C M, Jacobsen S E
Department of Immunology, Norwegian Radium Hospital, Oslo.
J Clin Invest. 1994 Jul;94(1):165-72. doi: 10.1172/JCI117303.
Stem cell factor (SCF), a key regulator of hematopoiesis, potently synergizes with a number of hematopoietic growth factors. However, little is known about growth factors capable of inhibiting the actions of SCF. TNF-alpha has been shown to act as a bidirectional regulator of myeloid cell proliferation and differentiation. This study was designed to examine interactions between TNF-alpha and SCF. Here, we demonstrate that TNF-alpha potently and directly inhibits SCF-stimulated proliferation of CD34+ hematopoietic progenitor cells. Furthermore, TNF-alpha blocked all colony formation stimulated by SCF in combination with granulocyte colony-stimulating factor (CSF) or CSF-1. The synergistic effect of SCF observed in combination with GM-CSF or IL-3 was also inhibited by TNF-alpha, resulting in colony numbers similar to those obtained in the absence of SCF. These effects of TNF-alpha were mediated through the p55 TNF receptor, whereas little or no inhibition was signaled through the p75 TNF receptor. Finally, TNF-alpha downregulated c-kit cell-surface expression on CD34+ bone marrow cells, and this was predominantly a p55 TNF receptor-mediated event as well.
干细胞因子(SCF)是造血的关键调节因子,能与多种造血生长因子产生强大的协同作用。然而,对于能够抑制SCF作用的生长因子却知之甚少。肿瘤坏死因子-α(TNF-α)已被证明是髓样细胞增殖和分化的双向调节因子。本研究旨在检测TNF-α与SCF之间的相互作用。在此,我们证明TNF-α能有效且直接地抑制SCF刺激的CD34+造血祖细胞的增殖。此外,TNF-α阻断了SCF与粒细胞集落刺激因子(CSF)或CSF-1联合刺激的所有集落形成。TNF-α也抑制了SCF与粒细胞-巨噬细胞集落刺激因子(GM-CSF)或白细胞介素-3联合时观察到的协同效应,导致集落数量与未添加SCF时相似。TNF-α的这些效应是通过p55 TNF受体介导的,而通过p75 TNF受体发出的抑制作用很小或没有。最后,TNF-α下调了CD34+骨髓细胞上c-kit细胞表面的表达,这主要也是一个由p55 TNF受体介导的事件。