Links between metabolism and apoptosis in mammalian cells: Applications for anti-apoptosis engineering

被引:68
作者
Majors, Brian S.
Betenbaugh, Michael J.
Chiang, Gisela G.
机构
[1] Johns Hopkins Univ, Dept Chem & Biomol Engn, Baltimore, MD 21218 USA
[2] Biogen Idec Inc, Cellular Engn, Cambridge, MA 02142 USA
关键词
metabolism; apoptosis; Bcl-2; mammalian cell culture; anti-apoptosis; cell engineering; mitochondria; Bcl-xL; calcium; glycolysis; hexokinase; VDAC;
D O I
10.1016/j.ymben.2007.05.003
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
Production of complex recombinant proteins requires the culture of mammalian cells in bioreactors. Inherent in these cultures is the problem of cell death, which can result from nutrient depletion, byproduct accumulation, and other bioreactor stresses which signal the cell to die through apoptosis, or programmed cell death. Apoptosis is a highly regulated pathway of both pro- and anti-apoptotic proteins that promote cell survival or death, and cell engineering efforts to inhibit the apoptosis pathway have led to increased culture viability and recombinant protein production. Originally, the exclusive function of many of these pathway proteins was believed to be binding at the mitochondria and regulating apoptosis through modulation of the mitochondria permeability. While this protein functionality does still hold true, it is now evident that these proteins also include roles in the metabolic processes of the mitochondria. Furthermore, apoptosis pathway proteins in other organelles within the cell may also both modulate apoptosis and metabolism. This review first details the known links that exist between apoptosis proteins and metabolic functions in the cytosol, mitochondria, and endoplasmic reticulum. Second, the review turns to look at potentially new cell engineering strategies that are linked to metabolism for improving cell culture viability and protein production. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:317 / 326
页数:10
相关论文
共 91 条
[61]   MITOCHONDRIAL CA2+ HOMEOSTASIS IN INTACT-CELLS [J].
RIZZUTO, R ;
BASTIANUTTO, C ;
BRINI, M ;
MURGIA, M ;
POZZAN, T .
JOURNAL OF CELL BIOLOGY, 1994, 126 (05) :1183-1194
[62]   Mitochondria as all-round players of the calcium game [J].
Rizzuto, R ;
Bernardi, P ;
Pozzan, T .
JOURNAL OF PHYSIOLOGY-LONDON, 2000, 529 (01) :37-47
[63]   REGULATION OF GLUCOSE-METABOLISM IN THE LUNG - HEXOKINASE-CATALYZED PHOSPHORYLATION, A RATE-LIMITING STEP [J].
SALOTRA, PT ;
SINGH, VN .
LIFE SCIENCES, 1982, 31 (08) :791-794
[64]   Study of caspase inhibitors for limiting death in mammalian cell culture [J].
Sauerwald, TM ;
Oyler, GA ;
Betenbaugh, MJ .
BIOTECHNOLOGY AND BIOENGINEERING, 2003, 81 (03) :329-340
[65]   Inhibiting apoptosis in mammalian cell culture using the caspase inhibitor XIAP and deletion mutants [J].
Sauerwald, TM ;
Betenbaugh, MJ ;
Oyler, GA .
BIOTECHNOLOGY AND BIOENGINEERING, 2002, 77 (06) :704-716
[66]   Regulation of death receptor-mediated apoptosis pathways [J].
Schmitz, I ;
Kirchhoff, S ;
Krammer, PH .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2000, 32 (11-12) :1123-1136
[67]   BH4 domain of antiapoptotic Bcl-2 family members closes voltage-dependent anion channel and inhibits apoptotic mitochondrial changes and cell death [J].
Shimizu, S ;
Konishi, A ;
Kodama, T ;
Tsujimoto, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (07) :3100-3105
[68]   Electrophysiological study of a novel large pore formed by Bax and the voltage-dependent anion channel that is permeable to cytochrome c [J].
Shimizu, S ;
Ide, T ;
Yanagida, T ;
Tsujimoto, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (16) :12321-12325
[69]  
Simpson NH, 1998, BIOTECHNOL BIOENG, V59, P90, DOI 10.1002/(SICI)1097-0290(19980705)59:1<90::AID-BIT12>3.0.CO
[70]  
2-6