Cell death in mammalian cell culture: molecular mechanisms and cell line engineering strategies

被引:102
作者
Krampe, Britta [1 ,2 ]
Al-Rubeai, Mohamed [1 ,2 ]
机构
[1] Univ Coll Dublin, Sch Chem & Bioproc Engn, Dublin 4, Ireland
[2] Univ Coll Dublin, Conway Inst Biomol & Biomed Res, Dublin 4, Ireland
关键词
Bcl-2; Apoptosis; Autophagy; Cell engineering; Signalling pathways; Cell death; BCL-2 FAMILY PROTEINS; ANTI-APOPTOTIC GENES; ENDOPLASMIC-RETICULUM; MONOCLONAL-ANTIBODY; CHO-CELLS; OVER-EXPRESSION; HYBRIDOMA CELLS; CHEMOSTAT CULTURES; BATCH CULTURES; ANIMAL-CELLS;
D O I
10.1007/s10616-010-9274-0
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
Cell death is a fundamentally important problem in cell lines used by the biopharmaceutical industry. Environmental stress, which can result from nutrient depletion, by-product accumulation and chemical agents, activates through signalling cascades regulators that promote death. The best known key regulators of death process are the Bcl-2 family proteins which constitute a critical intracellular checkpoint of apoptosis cell death within a common death pathway. Engineering of several members of the anti-apoptosis Bcl-2 family genes in several cell types has extended the knowledge of their molecular function and interaction with other proteins, and their regulation of cell death. In this review, we describe the various modes of cell death and their death pathways at molecular and organelle level and discuss the relevance of the growing knowledge of antiapoptotic engineering strategies to inhibit cell death and increase productivity in mammalian cell culture.
引用
收藏
页码:175 / 188
页数:14
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