Hsu H C, Thomas T, Seibold J R, Thomas T J
Program in Clinical Pharmacology, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, New Brunswick 08903.
Agents Actions. 1993;39 Spec No:C204-6. doi: 10.1007/BF01972767.
Upregulation of ornithine decarboxylase (ODC) activity and polyamine levels is found in the kidney of MRL-lpr/lpr (lpr) mouse, an animal model of lupus. To understand the molecular genetics of ODC regulation in lpr mouse, we analyzed ODC mRNA and activity in the kidney of lpr and normal BALB/c and MRL(-)+/+ mice. Although ODC activity was significantly higher in lpr kidney, its mRNA level was lower compared to normal strains, as measured by Northern blot hybridization. Treatment of lpr mouse with difluoromethylornithine (DFMO) reduced ODC activity in lpr kidney to the level of normal strains. In contrast, ODC mRNA level increased 12-fold by DFMO treatment. These results suggest that post-transcriptional modification of ODC in lpr genetic background might be responsible for increased ODC activity and polyamines. The beneficial effect of DFMO on murine lupus suggests a pathogenic role for altered ODC regulation in lpr mouse.
在狼疮动物模型MRL-lpr/lpr(lpr)小鼠的肾脏中发现鸟氨酸脱羧酶(ODC)活性和多胺水平上调。为了解lpr小鼠中ODC调控的分子遗传学,我们分析了lpr、正常BALB/c和MRL(-)+/+小鼠肾脏中的ODC mRNA和活性。通过Northern印迹杂交检测,虽然lpr小鼠肾脏中的ODC活性显著更高,但其mRNA水平与正常品系相比更低。用二氟甲基鸟氨酸(DFMO)处理lpr小鼠可将lpr小鼠肾脏中的ODC活性降低至正常品系水平。相反,DFMO处理使ODC mRNA水平增加了12倍。这些结果表明,在lpr遗传背景下ODC的转录后修饰可能是ODC活性和多胺增加的原因。DFMO对小鼠狼疮的有益作用表明lpr小鼠中ODC调控改变具有致病作用。