Jacobsen F W, Keller J R, Ruscetti F W, Veiby O P, Jacobsen S E
Department of Immunology, Norwegian Radium Hospital, Oslo.
Exp Hematol. 1995 Aug;23(9):990-5.
The present studies have investigated, for the first time, the synergistic effects of interleukin-4 (IL-4) and IL-11 on the growth of single murine bone marrow progenitor cells. These studies suggest that IL-4 and IL-11 are synergistic hematopoietic growth factors, enhancing colony formation of bone marrow progenitors from normal mice in the presence of colony-stimulating factors or stem cell factor, whereas neither IL-4 nor IL-11, alone or in combination, resulted in colony formation. However, in the presence of a neutralizing anti-TGF-beta antibody, IL-11 plus IL-4 induced clonal growth of primitive Lin-Sca1+ progenitors. Furthermore, here we report several observations extending the knowledge about IL-4 and IL-11 as synergistic factors. In addition to the established ability of IL-11 to enhance IL-3- and GM-CSF-induced colony formation, IL-11 also enhanced the number of G-CSF- and CSF-1-stimulated colonies of mature (Lin-) and primitive (Lin-Sca-1+) hematopoietic progenitors cultured at the single-cell level. In contrast, IL-4 bifunctionally regulated the growth of Lin- progenitors, whereas the growth of single Lin-Sca=1+ progenitors was unaffected or enhanced in the presence of IL-4. Finally, IL-4 and IL-11, in combination, potently synergized to enhance the high-proliferative-potential colony-forming cell colony formation of Lin-Sca-1+ progenitors in response to all four CSFs and to SCF.
本研究首次探究了白细胞介素-4(IL-4)和IL-11对单个小鼠骨髓祖细胞生长的协同作用。这些研究表明,IL-4和IL-11是协同造血生长因子,在存在集落刺激因子或干细胞因子的情况下,可增强正常小鼠骨髓祖细胞的集落形成,而单独或联合使用IL-4和IL-11均未导致集落形成。然而,在存在中和性抗转化生长因子-β抗体的情况下,IL-11加IL-4可诱导原始Lin-Sca1+祖细胞的克隆生长。此外,我们在此报告了一些观察结果,扩展了关于IL-4和IL-11作为协同因子的知识。除了已确定的IL-11增强IL-3和粒细胞-巨噬细胞集落刺激因子诱导的集落形成的能力外,IL-11还增加了在单细胞水平培养的成熟(Lin-)和原始(Lin-Sca-1+)造血祖细胞的粒细胞集落刺激因子和集落刺激因子-1刺激的集落数量。相比之下,IL-4对Lin-祖细胞的生长具有双相调节作用,而在存在IL-4的情况下,单个Lin-Sca=1+祖细胞的生长未受影响或增强。最后,IL-4和IL-11联合使用可有效协同作用,增强Lin-Sca-1+祖细胞对所有四种集落刺激因子和干细胞因子的高增殖潜能集落形成细胞集落形成。