Kim Myoung Ok, Kim Sung Hyun, Shin Mi Jung, Lee Dong Beom, Kim Tae Won, Kim Kil Soo, Ha Ji Hong, Lee Sanggyu, Park Yong Bok, Kim Sun Jung, Ryoo Zae Young
School of Life Sciences and Biotechnology, College of Natural Sciences, Kyungpook National University, Daegu 702-701, Korea.
Mol Cells. 2007 Feb 28;23(1):17-22.
We have expressed human erythropoietin (EPO) in transgenic mice using a recombinant EPO cDNA combined with a partial TPO construct. The gene was microinjected using standard techniques and five mice were detected as transgenic by PCR and further used as founders. The life span of the transgenic founders was much shorter than that of their normal littermates. Most of the tissues of the transgenic founders contained human EPO transcripts as judged by RT-PCR. Especially high expression levels were seen in the liver and lung. EPO protein levels in serum were examined by ELISA and ranged from 266, 414 mIU/ml. The number of red blood cell, white blood cell and hemoglobin in the hEPO transgenic mice was higher than in normal mice. These results indicate that overexpression of hEPO is deleterious and can provoke lung failure and erythrocytosis.
我们使用重组促红细胞生成素(EPO)cDNA与部分血小板生成素(TPO)构建体相结合,在转基因小鼠中表达了人促红细胞生成素(EPO)。采用标准技术对该基因进行显微注射,通过聚合酶链反应(PCR)检测到五只小鼠为转基因小鼠,并进一步用作奠基鼠。转基因奠基鼠的寿命比其正常同窝小鼠短得多。通过逆转录-聚合酶链反应(RT-PCR)判断,转基因奠基鼠的大多数组织都含有人类EPO转录本。在肝脏和肺中观察到特别高的表达水平。通过酶联免疫吸附测定(ELISA)检测血清中的EPO蛋白水平,范围为266至414毫国际单位/毫升。人促红细胞生成素(hEPO)转基因小鼠的红细胞、白细胞数量和血红蛋白含量高于正常小鼠。这些结果表明,hEPO的过度表达是有害的,可引发肺衰竭和红细胞增多症。