Supporting Aspartate Biosynthesis Is an Essential Function of Respiration in Proliferating Cells

被引:962
作者
Sullivan, Lucas B. [1 ,2 ]
Gui, Dan Y. [1 ,2 ]
Hosios, Aaron M. [1 ,2 ]
Bush, Lauren N. [1 ,2 ]
Freinkman, Elizaveta [3 ]
Vander Heiden, Matthew G. [1 ,2 ,4 ]
机构
[1] MIT, Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[2] MIT, Dept Biol, Cambridge, MA 02139 USA
[3] Whitehead Inst Biomed Res, Nine Cambridge Ctr, Cambridge, MA 02142 USA
[4] Dana Farber Canc Inst, Boston, MA 02115 USA
关键词
TUMOR-CELLS; MITOCHONDRIAL DYSFUNCTION; REDUCTIVE CARBOXYLATION; GLUTAMINE-METABOLISM; ALPHA-KETOGLUTARATE; AEROBIC GLYCOLYSIS; MAMMALIAN-CELLS; CANCER-CELLS; REDOX STATE; EXPRESSION;
D O I
10.1016/j.cell.2015.07.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Mitochondrial respiration is important for cell proliferation; however, the specific metabolic requirements fulfilled by respiration to support proliferation have not been defined. Here, we show that a major role of respiration in proliferating cells is to provide electron acceptors for aspartate synthesis. This finding is consistent with the observation that cells lacking a functional respiratory chain are auxotrophic for pyruvate, which serves as an exogenous electron acceptor. Further, the pyruvate requirement can be fulfilled with an alternative electron acceptor, alpha-ketobutyrate, which provides cells neither carbon nor ATP. Alpha-ketobutyrate restores proliferation when respiration is inhibited, suggesting that an alternative electron acceptor can substitute for respiration to support proliferation. We find that electron acceptors are limiting for producing aspartate, and supplying aspartate enables proliferation of respiration deficient cells in the absence of exogenous electron acceptors. Together, these data argue a major function of respiration in proliferating cells is to support aspartate synthesis.
引用
收藏
页码:552 / 563
页数:12
相关论文
共 50 条
[1]
HYPOXIA AND METABOLISM SERIES - TIMELINE The impact of O2 availability on human cancer [J].
Bertout, Jessica A. ;
Patel, Shetal A. ;
Simon, M. Celeste .
NATURE REVIEWS CANCER, 2008, 8 (12) :967-975
[2]
An Essential Role of the Mitochondrial Electron Transport Chain in Cell Proliferation Is to Enable Aspartate Synthesis [J].
Birsoy, Kivanc ;
Wang, Tim ;
Chen, Walter W. ;
Freinkman, Elizaveta ;
Abu-Remaileh, Monther ;
Sabatini, David M. .
CELL, 2015, 162 (03) :540-551
[3]
Assessing mitochondrial dysfunction in cells [J].
Brand, Martin D. ;
Nicholls, David G. .
BIOCHEMICAL JOURNAL, 2011, 435 :297-312
[4]
NAD+ as a Signaling Molecule Modulating Metabolism [J].
Canto, C. ;
Auwerx, J. .
METABOLISM AND DISEASE, 2011, 76 :291-298
[5]
Inhibition of ATPIF1 Ameliorates Severe Mitochondrial Respiratory Chain Dysfunction in Mammalian Cells [J].
Chen, Walter W. ;
Birsoy, Kivanc ;
Mihaylova, Maria M. ;
Snitkin, Harriet ;
Stasinski, Iwona ;
Yucel, Burcu ;
Bayraktar, Erol C. ;
Carette, Jan E. ;
Clish, Clary B. ;
Brummelkamp, Thijn R. ;
Sabatini, David D. ;
Sabatini, David M. .
CELL REPORTS, 2014, 7 (01) :27-34
[6]
Beyond aerobic glycolysis: Transformed cells can engage in glutamine metabolism that exceeds the requirement for protein and nucleotide synthesis [J].
DeBerardinis, Ralph J. ;
Mancuso, Anthony ;
Daikhin, Evgueni ;
Nissim, Ilana ;
Yudkoff, Marc ;
Wehrli, Suzanne ;
Thompson, Craig B. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (49) :19345-19350
[7]
Glutamine-driven oxidative phosphorylation is a major ATP source in transformed mammalian cells in both normoxia and hypoxia [J].
Fan, Jing ;
Kamphorst, Jurre J. ;
Mathew, Robin ;
Chung, Michelle K. ;
White, Eileen ;
Shlomi, Tomer ;
Rabinowitz, Joshua D. .
MOLECULAR SYSTEMS BIOLOGY, 2013, 9
[8]
Reductive glutamine metabolism is a function of the α-ketoglutarate to citrate ratio in cells [J].
Fendt, Sarah-Maria ;
Bell, Eric L. ;
Keibler, Mark A. ;
Olenchock, Benjamin A. ;
Mayers, Jared R. ;
Wasylenko, Thomas M. ;
Vokes, Natalie I. ;
Guarente, Leonard ;
Vander Heiden, Matthew G. ;
Stephanopoulos, Gregory .
NATURE COMMUNICATIONS, 2013, 4
[9]
Membrane potential-driven protein import into mitochondria -: The sorting sequence cytochrome b2 modulates the Δψ-dependence of translocation of the matrix-targeting sequence [J].
Geissler, A ;
Krimmer, T ;
Bömer, U ;
Guiard, B ;
Rassow, J ;
Pfanner, N .
MOLECULAR BIOLOGY OF THE CELL, 2000, 11 (11) :3977-3991
[10]
ON AUXOTROPHY FOR PYRIMIDINES OF RESPIRATION-DEFICIENT CHICK-EMBRYO CELLS [J].
GREGOIRE, M ;
MORAIS, R ;
QUILLIAM, MA ;
GRAVEL, D .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1984, 142 (01) :49-55