Zhang L, Eddy A, Teng Y T, Fritzler M, Kluppel M, Melet F, Bernstein A
Program in Molecular Biology and Cancer, Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, Ontario, Canada.
Mol Cell Biol. 1995 Dec;15(12):6961-70. doi: 10.1128/MCB.15.12.6961.
The proto-oncogene Fli-1 is a member of the ets family of transcription factor genes. Its high expression in the thymus and spleen and the presence of DNA binding sites for Fli-1 in a number of lymphoid cell-specific gene suggest that Fli-1 is involved in the regulation of lymphopoiesis. Activation of the Fli-1 gene by either chromosomal translocation or viral insertion leads to Ewing's sarcoma in humans and erythroleukemia in mice, respectively. Thus, Fli-1 is normally involved in pathways involved in the regulation of cell growth and differentiation. We have generated H-2Kk-Fli-1 transgenic mice that overexpress Fli-1 in various mouse tissues, with the highest levels of Fli-1 protein in the thymus and spleen. These Fli-1 transgenic mice developed a high incidence of a progressive immunological renal disease and ultimately died of renal failure caused by tubulointerstitial nephritis and immune-complex glomerulonephritis. The incidences of renal disease correlated with the levels of Fli-1 protein in lymphoid tissues of transgenic lines. The hypergammaglobulinemia, splenomegaly, B-cell hyperplasia, accumulation of abnormal CD3+ B220+ T lymphoid cells and CD5+ B220+ B cells in peripheral lymphoid tissues, and detection of various autoantibodies in the sera of diseased Fli-1 transgenic mice suggested the involvement of an immune dysfunction in the pathogenesis of the renal disease. In addition, splenic B cells from transgenic mice exhibited increased proliferation and prolonged survival in vitro in response to mitogens. Taken together, these data suggest that overexpression or ectopic expression of Fli-1 perturbs normal lymphoid cell function and programmed cell death. Thus, H-2Kk-Fli-1 transgenic mice may serve as a murine model for autoimmune disease in humans, such as systemic lupus erythematosus.
原癌基因Fli-1是转录因子基因ets家族的成员。它在胸腺和脾脏中高表达,并且在许多淋巴样细胞特异性基因中存在Fli-1的DNA结合位点,这表明Fli-1参与淋巴细胞生成的调节。通过染色体易位或病毒插入激活Fli-1基因分别导致人类的尤因肉瘤和小鼠的红白血病。因此,Fli-1通常参与细胞生长和分化调节的途径。我们构建了H-2Kk-Fli-1转基因小鼠,其在各种小鼠组织中过表达Fli-1,胸腺和脾脏中Fli-1蛋白水平最高。这些Fli-1转基因小鼠发生进行性免疫性肾病的发生率很高,最终死于由肾小管间质性肾炎和免疫复合物肾小球肾炎引起的肾衰竭。肾病的发生率与转基因品系淋巴组织中Fli-1蛋白的水平相关。患病的Fli-1转基因小鼠血清中的高球蛋白血症、脾肿大、B细胞增生、外周淋巴组织中异常的CD3+B220+T淋巴细胞和CD5+B220+B细胞的积累以及各种自身抗体的检测表明免疫功能障碍参与了肾病的发病机制。此外,转基因小鼠的脾B细胞在体外对有丝分裂原的反应中表现出增殖增加和存活时间延长。综上所述,这些数据表明Fli-1的过表达或异位表达扰乱了正常的淋巴样细胞功能和程序性细胞死亡。因此,H-2Kk-Fli-1转基因小鼠可作为人类自身免疫性疾病如系统性红斑狼疮的小鼠模型。