Hume D A, Pavli P, Donahue R E, Fidler I J
Department of Cell Biology, University of Texas M.D. Anderson Cancer Center, Houston 77030.
J Immunol. 1988 Nov 15;141(10):3405-9.
Human recombinant macrophage CSF (CSF-1) was administered i.v. to mice. After four daily injections there was a dose-dependent increase in the responsiveness of bone marrow cells from the treated animals to CSF-1 in vitro. At the highest dose tested (20,000 U/day) there was a selective 10-fold increase in the circulating population of mature monocytes. CSF-1 treatment also increased the macrophage content of the liver and peritoneal cavity and caused splenomegaly. The macrophages isolated from the peritoneum of CSF-1-treated animals were larger and expressed higher levels of the macrophage-specific F4/80 Ag. These data demonstrate that CSF-1 can act as a circulating regulator of the mononuclear phagocyte system.
将人重组巨噬细胞集落刺激因子(CSF-1)静脉注射给小鼠。每日注射四次后,处理组动物骨髓细胞对CSF-1的体外反应性呈剂量依赖性增加。在测试的最高剂量(20,000 U/天)下,成熟单核细胞的循环群体选择性增加了10倍。CSF-1处理还增加了肝脏和腹腔中的巨噬细胞含量,并导致脾肿大。从CSF-1处理动物的腹膜中分离出的巨噬细胞更大,并且表达更高水平的巨噬细胞特异性F4/80抗原。这些数据表明CSF-1可以作为单核吞噬细胞系统的循环调节剂。