Johnson G R, Gonda T J, Metcalf D, Hariharan I K, Cory S
Walter and Eliza Hall Institute of Medical Research, PO Royal Melbourne Hospital, Australia.
EMBO J. 1989 Feb;8(2):441-8. doi: 10.1002/j.1460-2075.1989.tb03396.x.
Murine bone marrow cells infected with a novel recombinant retrovirus, MPZen(GM-CSF), were engrafted into lethally irradiated recipients. The transplanted animals developed extremely high circulating levels of GM-CSF (up to 3 x 10(5) units/ml), and greatly elevated peripheral nucleated cell counts (up to 110 x 10(6) per ml). Their haemopoietic tissues contained GM-CSF proviral DNA and produced substantial levels of GM-CSF. The mice died within 4 weeks of transplantation with extensive neutrophil and macrophage infiltration of the spleen, lung, liver and peritoneal cavity and significant infiltration of both heart and skeletal muscle by neutrophils, macrophages and eosinophils. The thymus and lymph nodes were deficient in lymphoid cells. No disease occurred when infected cells from haemopoietic tissues of the primary transplanted animals were injected into normal or sub-lethally irradiated mice. Dysregulated GM-CSF expression by haemopoietic cells thus produces a fatal albeit non-neoplastic myeloproliferative syndrome.
将感染新型重组逆转录病毒MPZen(GM-CSF)的小鼠骨髓细胞移植到接受致死剂量照射的受体体内。移植后的动物循环血液中GM-CSF水平极高(高达3×10⁵单位/毫升),外周有核细胞计数大幅升高(高达110×10⁶/毫升)。它们的造血组织含有GM-CSF前病毒DNA,并产生大量的GM-CSF。这些小鼠在移植后4周内死亡,脾脏、肺、肝脏和腹腔有广泛的中性粒细胞和巨噬细胞浸润,心脏和骨骼肌有大量中性粒细胞、巨噬细胞和嗜酸性粒细胞浸润。胸腺和淋巴结缺乏淋巴细胞。将初次移植动物造血组织中的感染细胞注射到正常或接受亚致死剂量照射的小鼠体内时,未发生疾病。因此,造血细胞中GM-CSF表达失调会产生一种致命的、尽管是非肿瘤性的骨髓增殖综合征。