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
[1]   Apoptosis in cell culture [J].
Al-Rubeai, M ;
Singh, RP .
CURRENT OPINION IN BIOTECHNOLOGY, 1998, 9 (02) :152-156
[2]   Life and death in mammalian cell culture: strategies for apoptosis inhibition [J].
Arden, N ;
Betenbaugh, MJ .
TRENDS IN BIOTECHNOLOGY, 2004, 22 (04) :174-180
[3]   Chemical caspase inhibitors enhance cell culture viabilities and protein titer [J].
Arden, Nilou ;
Ahn, Shin-hyung ;
Vaz, Wayne ;
Rhodes, Malcolm ;
Hancock, Christina ;
Abitorabi, M. Abi ;
Betenbaugh, Michael J. .
BIOTECHNOLOGY PROGRESS, 2007, 23 (02) :506-511
[4]   Targeting death and decoy receptors of the tumour-necrosis factor superfamily [J].
Ashkenazi, A .
NATURE REVIEWS CANCER, 2002, 2 (06) :420-430
[5]   In self-defence: Hexokinase promotes voltage-dependent anion channel closure and prevents mitochondria-mediated apoptotic cell death [J].
Azoulay-Zohar, H ;
Israelson, A ;
Abu-Hamad, S ;
Shoshan-Barmatz, V .
BIOCHEMICAL JOURNAL, 2004, 377 :347-355
[6]  
Belzacq AS, 2003, CANCER RES, V63, P541
[7]  
Burteau CC, 2003, IN VITRO CELL DEV-AN, V39, P291
[8]  
BUSTAMANTE E, 1981, J BIOL CHEM, V256, P8699
[9]   HIGH AEROBIC GLYCOLYSIS OF RAT HEPATOMA-CELLS IN CULTURE - ROLE OF MITOCHONDRIAL HEXOKINASE - (L-LACTIC ACID-D-GLUCOSE-D-GALACTOSE-LIVER-NEOPLASIA) [J].
BUSTAMANTE, E ;
PEDERSEN, PL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (09) :3735-3739
[10]   Prolongation of murine hybridoma cell survival in stationary batch culture by Bcl-xL expression [J].
Charbonneau, JR ;
Gauthier, ER .
CYTOTECHNOLOGY, 2000, 34 (1-2) :131-139