Peroxisome proliferator-activated receptor-γ coactivator 1-α (PGC1α) is a metabolic regulator of intestinal epithelial cell fate

被引:133
作者
D'Errico, Ilenia [1 ,2 ]
Salvatore, Lorena [1 ,2 ]
Murzilli, Stefania [1 ,2 ]
Lo Sasso, Giuseppe [1 ,2 ]
Latorre, Dominga [3 ]
Martelli, Nicola [1 ,2 ]
Egorova, Anastasia V. [4 ]
Polishuck, Roman [4 ]
Madeyski-Bengtson, Katja [5 ]
Lelliott, Christopher [6 ]
Vidal-Puig, Antonio J. [7 ]
Seibel, Peter [8 ]
Villani, Gaetano [3 ]
Moschetta, Antonio [1 ,2 ]
机构
[1] Consorzio Mario Negri Sud, Dept Translat Pharmacol, Lab Lipid Metab & Canc, I-66030 Santa Maria Imbaro, Chieti, Italy
[2] Univ Bari, Clin Med A Murri, I-70124 Bari, Italy
[3] Univ Bari, Dept Med Biochem Biol & Phys, I-70124 Bari, Italy
[4] Consorzio Mario Negri Sud, Dept Cell Biol & Oncol, I-66030 Santa Maria Imbaro, Chieti, Italy
[5] AstraZeneca Res & Dev, AstraZeneca Transgen & Comparat Gen, SE-43183 Molndal, Sweden
[6] AstraZeneca Res & Dev, Dept Biosci, SE-43183 Molndal, Sweden
[7] Univ Cambridge, Inst Metab Sci, Metab Res Labs, Cambridge CB2 0QQ, England
[8] Univ Leipzig, Ctr Biotechnol & Biomed, Dept Mol Cell Therapy, D-04103 Leipzig, Germany
关键词
colon cancer; medical physiology; metabolism; mitochondria; nuclear receptors; CYTOCHROME-C-OXIDASE; CONTROLLING MITOCHONDRIAL BIOGENESIS; TRANSCRIPTIONAL COACTIVATOR; COLORECTAL-CANCER; IN-VIVO; ADENOMATOUS POLYPOSIS; ENDOTHELIAL-CELLS; RAT INTESTINE; PPAR-GAMMA; PGC-1-ALPHA;
D O I
10.1073/pnas.1016354108
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
Peroxisome proliferator-activated receptor-gamma coactivator 1-alpha (PGC1 alpha) is a transcriptional coactivator able to up-regulate mitochondrial biogenesis, respiratory capacity, oxidative phosphorylation, and fatty acid beta-oxidation with the final aim of providing a more efficient pathway for aerobic energy production. In the continuously renewed intestinal epithelium, proliferative cells in the crypts migrate along the villus axis and differentiate into mature enterocytes, increasing their respiratory capacity and finally undergoing apoptosis. Here we show that in the intestinal epithelial surface, PGC1 alpha drives mitochondrial biogenesis and respiration in the presence of reduced antioxidant enzyme activities, thus determining the accumulation of reactive oxygen species and fostering the fate of enterocytes toward apoptosis. Combining gain-and loss-of-function genetic approaches in human cells and mouse models of intestinal cancer, we present an intriguing scenario whereby PGC1 alpha regulates enterocyte cell fate and protects against tumorigenesis.
引用
收藏
页码:6603 / 6608
页数:6
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