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强力霉素调节钙连蛋白和钙网蛋白表达对重组中国仓鼠卵巢细胞特异性血小板生成素产生能力的影响。

Effect of doxycycline-regulated calnexin and calreticulin expression on specific thrombopoietin productivity of recombinant Chinese hamster ovary cells.

作者信息

Chung Joo Young, Lim Seung Wook, Hong Yeon Joo, Hwang Sun Ok, Lee Gyun Min

机构信息

Department of Biological Sciences, Korea Advanced Institute of Science and Technology, 373-1 Kusong-Dong, Yusong-Gu, Daejon 305-701, Korea.

出版信息

Biotechnol Bioeng. 2004 Mar 5;85(5):539-46. doi: 10.1002/bit.10919.

DOI:10.1002/bit.10919
PMID:14760694
Abstract

In an attempt to increase the specific thrombopoietin (TPO) productivity (q(TPO)) of recombinant Chinese hamster ovary (rCHO) cells (CHO-TPO), the effect of expression level of calnexin (CNX) and calreticulin (CRT) on q(TPO) was investigated. To control both CNX and CRT expression levels simultaneously, the Tet-Off system was first introduced in CHO-TPO cells, and stable Tet-Off cells (TPO-Tet-Off) were screened by luciferase assay. The doxycycline-regulated CNX and CRT expression system in rCHO cells (TPO-CNX/CRT) was established by cotransfection of CNX and CRT expression vector and pTK-Hyg vector into TPO-Tet-Off cells and subsequent screening by Western blot analysis of CNX and CRT. The expression levels of CNX and CRT in TPO-CNX/CRT cells could be tightly controlled by adding different concentrations of doxycycline to a culture medium. Compared with the basal level (2 microg/mL doxycyline), a 2.9-fold increase in CNX expression and a 2.8-fold increase in CRT expression were obtained in the absence of doxycycline. This, in turn, resulted in a 1.9-fold increase in q(TPO), not inhibiting cell growth or changing in vivo biological activity of TPO. Taken together, these results demonstrate that a simultaneous overexpression of CNX and CRT can increase the q(TPO) of rCHO cells.

摘要

为提高重组中国仓鼠卵巢细胞(rCHO)(CHO-TPO)中特异性血小板生成素(TPO)的产量(q(TPO)),研究了钙连蛋白(CNX)和钙网蛋白(CRT)的表达水平对q(TPO)的影响。为同时控制CNX和CRT的表达水平,首先在CHO-TPO细胞中引入Tet-Off系统,并通过荧光素酶测定筛选出稳定的Tet-Off细胞(TPO-Tet-Off)。通过将CNX和CRT表达载体与pTK-Hyg载体共转染到TPO-Tet-Off细胞中,随后通过对CNX和CRT的蛋白质免疫印迹分析进行筛选,建立了rCHO细胞中强力霉素调节的CNX和CRT表达系统(TPO-CNX/CRT)。通过向培养基中添加不同浓度的强力霉素,可以严格控制TPO-CNX/CRT细胞中CNX和CRT的表达水平。与基础水平(2μg/mL强力霉素)相比,在无强力霉素的情况下,CNX表达增加了2.9倍,CRT表达增加了2.8倍。这进而导致q(TPO)增加了1.9倍,且不抑制细胞生长或改变TPO的体内生物学活性。综上所述,这些结果表明,同时过表达CNX和CRT可提高rCHO细胞的q(TPO)。

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