Kunaparaju Rajkumar, Liao Mimi, Sunstrom Noelle-Anne
School of Biotechnology & Biomolecular Sciences, University of New South Wales, Sydney NSW, Australia.
Biotechnol Bioeng. 2005 Sep 20;91(6):670-7. doi: 10.1002/bit.20534.
This study describes the development of a transient expression system for CHO cells based on autonomous replication and retention of transfected plasmid DNA. A transient expression system that allows extrachromosomal amplification of plasmids permits more plasmid copies to persist in the transfected cell throughout the production phase leading to a significant increase in transgene expression. The expression system, named Epi-CHO comprises (1) a CHO-K1 cell line stably transfected with the Polyomavirus (Py) large T (LT) antigen gene (PyLT) and (2) a DNA expression vector, pPyEBV encoding the Py origin (PyOri) for autonomous plasmid amplification and encoding Epstein-Barr Virus (EBV) nuclear antigen-1 (EBNA-1) and OriP for plasmid retention. The CHO-K1 cell line expressing PyLT, named CHO-T was adapted to suspension growth in serum-free media to facilitate large-scale transient transfection and recombinant gene expression. Enhanced green fluorescent protein (EGFP) and human growth hormone (hGH) were used as reporter proteins to demonstrate transgene expression and productivity. Transfection of suspension-growing CHO-T cells with the vector pPyEBV encoding hGH resulted in a final concentration of 75 mg L(-1) of hGH in culture supernatants 11 days following transfection.
本研究描述了一种基于转染质粒DNA的自主复制和保留的CHO细胞瞬时表达系统的开发。一种允许质粒染色体外扩增的瞬时表达系统可使更多的质粒拷贝在整个生产阶段持续存在于转染细胞中,从而导致转基因表达显著增加。该表达系统名为Epi-CHO,包括:(1)稳定转染多瘤病毒(Py)大T(LT)抗原基因(PyLT)的CHO-K1细胞系;(2)DNA表达载体pPyEBV,其编码用于自主质粒扩增的Py起源(PyOri),并编码EB病毒(EBV)核抗原-1(EBNA-1)和用于质粒保留的OriP。表达PyLT的CHO-K1细胞系命名为CHO-T,已适应在无血清培养基中悬浮生长,以促进大规模瞬时转染和重组基因表达。增强型绿色荧光蛋白(EGFP)和人生长激素(hGH)用作报告蛋白,以证明转基因表达和生产力。用编码hGH的载体pPyEBV转染悬浮生长的CHO-T细胞,转染后11天,培养上清液中hGH的最终浓度为75 mg L(-1)。