Bcl-xL overexpression delays the onset of autophagy and apoptosis in hyperosmotic recombinant Chinese hamster ovary cell cultures

被引:15
|
作者
Han, Young Kue [1 ]
Ha, Tae Kwang [1 ]
Kim, Yeon-Gu [1 ]
Lee, Gyun Min [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Grad Sch Nanosci & Technol WCU, Dept Biol Sci, Taejon 305701, South Korea
关键词
Bcl-x(L); Autophagy; Apoptosis; rCHO cells; Hyperosmolality; Fed-batch culture; MONOCLONAL-ANTIBODY PRODUCTION; CHO-CELLS; OSMOLALITY; PRESSURE; JNK; PHOSPHORYLATION; TRANSLOCATION; MITOCHONDRIA; STRESS; BCL-2;
D O I
10.1016/j.jbiotec.2011.07.032
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Hyperosmolality in recombinant Chinese hamster ovary (rCHO) cell cultures induces autophagy and apoptosis. To investigate the effect of Bcl-x(L) overexpression on autophagy and apoptosis in hyperosmotic rCHO cell cultures, an erythropoietin (EPO)-producing rCHO cell line with regulated Bcl-x(L) overexpression was subjected to hyperosmolality resulting from NaCl addition in a batch culture and nutrient supplementation in a fed-batch culture. In the batch culture, Bcl-x(L) overexpression suppressed apoptosis, as evidenced by a decreased amount of cleaved caspase-7 and PARP. Concurrently, Bcl-x(L) overexpression also delayed autophagy, as indicated by reduced LC3 conversion, from LC3-I to LC3-II. As a result, the cell viability and EPO production were improved by Bcl-x(L) overexpression. In the fed-batch culture, the simultaneous application of Bcl-x(L) overexpression and nutrient feeding increased the culture longevity and maximum EPO concentration. Taken together, Bcl-x(L) overexpression delayed autophagy and apoptosis in hyperosmotic rCHO cell cultures, resulting in increased EPO production. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:52 / 55
页数:4
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