Just U, Stocking C, Spooncer E, Dexter T M, Ostertag W
Heinrich-Pette-Institut für Experimentelle Virologie und Immunologie, Universität Hamburg, Federal Republic of Germany.
Cell. 1991 Mar 22;64(6):1163-73. doi: 10.1016/0092-8674(91)90271-y.
Multipotent murine stem cell lines (FDC-Pmix) depend on IL-3 for self-renewal and proliferation and can be induced to differentiate into multiple hematopoietic lineages. Single FDC-Pmix cells infected with retroviral vectors expressing GM-CSF are induced to differentiate into granulocytes and macrophages. This results in a complete loss of clonogenic cells if IL-3 is not exogenously supplied; however, multipotent variants can be selected that do not terminally differentiate if cells are kept in the presence of IL-3. Unidirectional and synchronous granulocyte and macrophage differentiation accompanied with loss of self-renewal capacity is induced when IL-3 is removed. Our data indicate that activation of the GM-CSF receptor induces differentiation of stem cells by an instructive mechanism that can be blocked by the activated IL-3 receptor. A model of how receptors can induce proliferation and cell-specific differentiation by two separate pathways is discussed.
多能小鼠干细胞系(FDC-Pmix)的自我更新和增殖依赖于白细胞介素-3(IL-3),并且可以被诱导分化为多种造血谱系。感染了表达粒细胞-巨噬细胞集落刺激因子(GM-CSF)的逆转录病毒载体的单个FDC-Pmix细胞被诱导分化为粒细胞和巨噬细胞。如果不外源提供IL-3,这会导致克隆形成细胞完全丧失;然而,如果细胞保持在IL-3存在的环境中,可以选择出不会终末分化的多能变体。当去除IL-3时,会诱导粒细胞和巨噬细胞进行单向且同步的分化,并伴随着自我更新能力的丧失。我们的数据表明,GM-CSF受体的激活通过一种可被激活的IL-3受体阻断的诱导机制诱导干细胞分化。本文讨论了受体如何通过两条独立途径诱导增殖和细胞特异性分化的模型。