Lang R A, Metcalf D, Cuthbertson R A, Lyons I, Stanley E, Kelso A, Kannourakis G, Williamson D J, Klintworth G K, Gonda T J
Ludwig Institute for Cancer Research, Melbourne Tumour Biology Branch, Royal Melbourne Hospital, Victoria, Australia.
Cell. 1987 Nov 20;51(4):675-86. doi: 10.1016/0092-8674(87)90136-x.
Transgenic mice carrying the murine granulocyte-macrophage colony stimulating factor (GM-CSF) gene expressed from a retroviral promoter exhibit elevated levels of GM-CSF in the serum, urine, peritoneal cavity, and eye. The eyes of transgenic mice are opaque, contain accumulations of macrophages, and develop retinal damage. Similarly, lesions containing macrophages develop in striated muscle. The mice also display an accumulation of large, often multinucleate, activated macrophages in the peritoneal and pleural cavities. The transgene is transcribed in peritoneal cells, as well as in eyes and infiltrated striated muscle. A high proportion of transgenic mice die with muscle wasting when aged 2-4 months, possibly because of macrophage activation resulting from the high levels of GM-CSF.
携带从逆转录病毒启动子表达的鼠粒细胞-巨噬细胞集落刺激因子(GM-CSF)基因的转基因小鼠,其血清、尿液、腹腔和眼睛中的GM-CSF水平升高。转基因小鼠的眼睛不透明,含有巨噬细胞聚集物,并出现视网膜损伤。同样,横纹肌中也会出现含有巨噬细胞的病变。这些小鼠在腹腔和胸腔中还表现出大量通常为多核的活化巨噬细胞的聚集。转基因在腹膜细胞、眼睛和浸润的横纹肌中转录。高比例的转基因小鼠在2至4个月大时死于肌肉萎缩,这可能是由于高水平的GM-CSF导致巨噬细胞活化所致。