
Cell Metabolism, Journal Year: 2014, Volume and Issue: 20(1), P. 61 - 72
Published: June 12, 2014
Language: Английский
Cell Metabolism, Journal Year: 2014, Volume and Issue: 20(1), P. 61 - 72
Published: June 12, 2014
Language: Английский
Cell, Journal Year: 2012, Volume and Issue: 149(2), P. 274 - 293
Published: April 1, 2012
Language: Английский
Citations
7796Cell, Journal Year: 2017, Volume and Issue: 168(6), P. 960 - 976
Published: March 1, 2017
Language: Английский
Citations
6302Cell, Journal Year: 2017, Volume and Issue: 169(3), P. 381 - 405
Published: April 1, 2017
Language: Английский
Citations
3027Cancer Cell, Journal Year: 2012, Volume and Issue: 21(3), P. 297 - 308
Published: March 1, 2012
Language: Английский
Citations
2935Science Advances, Journal Year: 2016, Volume and Issue: 2(5)
Published: May 6, 2016
Researchers provide a conceptual framework to understand current knowledge of the fundamentals cancer metabolism.
Language: Английский
Citations
2516Cell, Journal Year: 2017, Volume and Issue: 170(4), P. 605 - 635
Published: Aug. 1, 2017
Language: Английский
Citations
2171Nature Reviews Molecular Cell Biology, Journal Year: 2020, Volume and Issue: 21(4), P. 183 - 203
Published: Jan. 14, 2020
Language: Английский
Citations
2070Cell Metabolism, Journal Year: 2012, Volume and Issue: 15(6), P. 848 - 860
Published: May 17, 2012
Language: Английский
Citations
1754The Journal of Experimental Medicine, Journal Year: 2011, Volume and Issue: 208(7), P. 1367 - 1376
Published: June 27, 2011
Upon antigen stimulation, the bioenergetic demands of T cells increase dramatically over resting state. Although a role for metabolic switch to glycolysis has been suggested support increased anabolic activities and facilitate cell growth proliferation, whether cellular metabolism controls lineage choices remains poorly understood. We report that glycolytic pathway is actively regulated during differentiation inflammatory TH17 Foxp3-expressing regulatory (Treg cells) fate determination. but not Treg cell–inducing conditions resulted in strong up-regulation activity induction enzymes. Blocking inhibited development while promoting generation. Moreover, transcription factor hypoxia-inducible 1α (HIF1α) was selectively expressed its required signaling through mTOR, central regulator metabolism. HIF1α–dependent transcriptional program important mediating activity, thereby contributing between cells. Lack HIF1α diminished enhanced protected mice from autoimmune neuroinflammation. Our studies demonstrate orchestrates checkpoint
Language: Английский
Citations
1580Nature reviews. Cancer, Journal Year: 2019, Volume and Issue: 20(2), P. 74 - 88
Published: Nov. 4, 2019
Language: Английский
Citations
1521