Ran P, Ouyang N, Zhong N, Chen S
Guangzhou Institute of Respiratory Disease.
Zhongguo Ying Yong Sheng Li Xue Za Zhi. 1997 Feb;13(1):21-4.
This paper is to investigate the expression of oncogene jun fos and myb mRNA in the lung of rats exposed to chronic hypoxia. 15 SD rats were put in low oxygen chamber (FiO2 = 0.1), 8 hrs daily for 1, 2 and 3 weeks. Five rats breathing room air served as control. Oncogene expression in lung tissue assessed by the use of in situ hybridization. The results showed that (1) there was a slight expression of jun mRNA but not fos and myb mRNA in the control normoxic rats' lung; (2) it was found that a less expression of jun mRNA in lung after 1 week hypoxia, but after 2 week hypoxia jun mRNA elevated again and significantly increased after 3 week hypoxia as compared with that in normoxia; (3) the oncogene myb mRNA expression showed significant increase in 1 and 2 week hypoxia and returned to normal status in 3 week hypoxia; (4) after 1 to 3 week hypoxia, a significant increased expression of fos mRNA was found as compared with that in normoxia. It is suggested hypoxia may induce increased expression of proto-oncogene jun myb and fos, which may be related to proliferation of pulmonary arterial smooth muscle cells and fibroblasts.
本文旨在研究慢性缺氧大鼠肺组织中癌基因jun、fos和myb mRNA的表达情况。将15只SD大鼠置于低氧舱(吸入氧分数FiO2 = 0.1)中,每天8小时,分别持续1、2和3周。5只呼吸空气的大鼠作为对照。采用原位杂交法评估肺组织中的癌基因表达。结果显示:(1)在正常氧合的对照大鼠肺组织中有jun mRNA的轻微表达,但无fos和myb mRNA的表达;(2)发现缺氧1周后肺组织中jun mRNA表达减少,但缺氧2周后jun mRNA再次升高,且缺氧3周后与正常氧合相比显著增加;(3)癌基因myb mRNA表达在缺氧1周和2周时显著增加,缺氧3周时恢复至正常水平;(4)缺氧1至3周后,与正常氧合相比,fos mRNA表达显著增加。提示缺氧可能诱导原癌基因jun、myb和fos表达增加,这可能与肺动脉平滑肌细胞和成纤维细胞的增殖有关。