Effect of Fatty Acids on Human Bone Marrow Mesenchymal Stem Cell Energy Metabolism and Survival

被引:58
作者
Fillmore, Natasha [1 ]
Huqi, Alda [1 ]
Jaswal, Jagdip S. [1 ]
Mori, Jun [1 ]
Paulin, Roxane [1 ]
Haromy, Alois [1 ]
Onay-Besikci, Arzu [1 ]
Ionescu, Lavinia [1 ]
Thebaud, Bernard [1 ]
Michelakis, Evangelos [1 ]
Lopaschuk, Gary D. [1 ]
机构
[1] Univ Alberta, Cardiovasc Res Ctr, Mazankowski Alberta Heart Inst, Edmonton, AB, Canada
来源
PLOS ONE | 2015年 / 10卷 / 03期
基金
加拿大健康研究院;
关键词
PROLIFERATION; APOPTOSIS; DIFFERENTIATION; GROWTH; AKT; DEHYDROGENASE; ACTIVATION; OXIDATION; PATHWAY; STRESS;
D O I
10.1371/journal.pone.0120257
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Successful stem cell therapy requires the optimal proliferation, engraftment, and differentiation of stem cells into the desired cell lineage of tissues. However, stem cell therapy clinical trials to date have had limited success, suggesting that a better understanding of stem cell biology is needed. This includes a better understanding of stem cell energy metabolism because of the importance of energy metabolism in stem cell proliferation and differentiation. We report here the first direct evidence that human bone marrow mesenchymal stem cell (BMMSC) energy metabolism is highly glycolytic with low rates of mitochondrial oxidative metabolism. The contribution of glycolysis to ATP production is greater than 97% in undifferentiated BMMSCs, while glucose and fatty acid oxidation combined only contribute 3% of ATP production. We also assessed the effect of physiological levels of fatty acids on human BMMSC survival and energy metabolism. We found that the saturated fatty acid palmitate induces BMMSC apoptosis and decreases proliferation, an effect prevented by the unsaturated fatty acid oleate. Interestingly, chronic exposure of human BMMSCs to physiological levels of palmitate (for 24 hr) reduces palmitate oxidation rates. This decrease in palmitate oxidation is prevented by chronic exposure of the BMMSCs to oleate. These results suggest that reducing saturated fatty acid oxidation can decrease human BMMSC proliferation and cause cell death. These results also suggest that saturated fatty acids may be involved in the long-term impairment of BMMSC survival in vivo.
引用
收藏
页数:17
相关论文
共 47 条
[1]   Human Embryonic Stem Cells and Embryonal Carcinoma Cells Have Overlapping and Distinct Metabolic Signatures [J].
Abu Dawud, Raed ;
Schreiber, Kerstin ;
Schomburg, Dietmar ;
Adjaye, James .
PLOS ONE, 2012, 7 (06)
[2]   Guided Cardiopoiesis Enhances Therapeutic Benefit of Bone Marrow Human Mesenchymal Stem Cells in Chronic Myocardial Infarction [J].
Behfar, Atta ;
Yamada, Satsuki ;
Crespo-Diaz, Ruben ;
Nesbitt, Jonathan J. ;
Rowe, Lois A. ;
Perez-Terzic, Carmen ;
Gaussin, Vinciane ;
Homsy, Christian ;
Bartunek, Jozef ;
Terzic, Andre .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2010, 56 (09) :721-734
[3]   A mitochondria-K+ channel axis is suppressed in cancer and its normalization promotes apoptosis and inhibits cancer growth [J].
Bonnet, Sebastien ;
Archer, Stephen L. ;
Allalunis-Turner, Joan ;
Haromy, Alois ;
Beaulieu, Christian ;
Thompson, Richard ;
Lee, Christopher T. ;
Lopaschuk, Gary D. ;
Puttagunta, Lakshmi ;
Bonnet, Sandra ;
Harry, Gwyneth ;
Hashimoto, Kyoko ;
Porter, Christopher J. ;
Andrade, Miguel A. ;
Thebaud, Bernard ;
Michelakis, Evangelos D. .
CANCER CELL, 2007, 11 (01) :37-51
[4]   QUALITY-CONTROL STUDIES ON FETAL BOVINE SERUM USED IN TISSUE-CULTURE [J].
BOONE, CW ;
CARUSO, TD ;
KAZAM, E ;
MANTEL, N ;
STEVENSO.RE .
IN VITRO-JOURNAL OF THE TISSUE CULTURE ASSOCIATION, 1971, 7 (03) :174-&
[5]   Metabolic regulation of stem cell function [J].
Burgess, R. J. ;
Agathocleous, M. ;
Morrison, S. J. .
JOURNAL OF INTERNAL MEDICINE, 2014, 276 (01) :12-24
[6]   The glucose dependence of Akt-transformed cells can be reversed by pharmacologic activation of fatty acid β-oxidation [J].
Buzzai, M ;
Bauer, DE ;
Jones, RG ;
DeBerardinis, RJ ;
Hatzivassiliou, G ;
Elstrom, RL ;
Thompson, CB .
ONCOGENE, 2005, 24 (26) :4165-4173
[7]   Increased Lipogenesis, Induced by AKT-mTORC1-RPS6 Signaling, Promotes Development of Human Hepatocellular Carcinoma [J].
Calvisi, Diego F. ;
Wang, Chunmei ;
Ho, Coral ;
Ladu, Sara ;
Lee, Susie A. ;
Mattu, Sandra ;
Destefanis, Giulia ;
Delogu, Salvatore ;
Zimmermann, Antje ;
Ericsson, Johan ;
Brozzetti, Stefania ;
Staniscia, Tommaso ;
Chen, Xin ;
Dombrowski, Frank ;
Evert, Matthias .
GASTROENTEROLOGY, 2011, 140 (03) :1071-U542
[8]   Coordinated changes of mitochondrial biogenesis and antioxidant enzymes during osteogenic differentiation of human mesenchymal stem cells [J].
Chen, Chien-Tsun ;
Shih, Yu-Ru V. ;
Kuo, Tom K. ;
Lee, Oscar K. ;
Wei, Yau-Huei .
STEM CELLS, 2008, 26 (04) :960-968
[9]   Mitochondrial oxidative metabolism is required for the cardiac differentiation of stem cells [J].
Chung S. ;
Dzeja P.P. ;
Faustino R.S. ;
Perez-Terzic C. ;
Behfar A. ;
Terzic A. .
Nature Clinical Practice Cardiovascular Medicine, 2007, 4 (Suppl 1) :S60-S67
[10]   Glycolytic network restructuring integral to the energetics of embryonic stem cell cardiac differentiation [J].
Chung, Susan ;
Arrell, D. Kent ;
Faustino, Randolph S. ;
Terzic, Andre ;
Dzeja, Petras P. .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2010, 48 (04) :725-734