Loss of Mitochondrial Pyruvate Carrier 2 in the Liver Leads to Defects in Gluconeogenesis and Compensation via Pyruvate-Alanine Cycling-Reference-Cited by-同舟云学术

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Loss of Mitochondrial Pyruvate Carrier 2 in the Liver Leads to Defects in Gluconeogenesis and Compensation via Pyruvate-Alanine Cycling

Published:2015-10 Issue:4 Volume:22 Page:682-694
ISSN:1550-4131
Container-title:Cell Metabolism
language:en
Short-container-title:Cell Metabolism

Author:

McCommis Kyle S.,Chen Zhouji,Fu Xiaorong,McDonald William G.,Colca Jerry R.,Kletzien Rolf F.,Burgess Shawn C.,Finck Brian N.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Physiology

Reference46 articles.

1. Comparative effects of englitazone and glyburide on gluconeogenesis and glycolysis in the isolated perfused rat liver;Adams;Biochem. Pharmacol.,1998

2. A mitochondrial pyruvate carrier required for pyruvate uptake in yeast, Drosophila, and humans;Bricker;Science,2012

3. Diminished hepatic gluconeogenesis via defects in tricarboxylic acid cycle flux in peroxisome proliferator-activated receptor gamma coactivator-1alpha (PGC-1alpha)-deficient mice;Burgess;J. Biol. Chem.,2006

4. Development of a method for rapid quantitation of amino acids by liquid chromatography-tandem mass spectrometry (LC-MSMS) in plasma;Casetta;Clin. Chem. Lab. Med.,2000

5. Alterations in hepatic metabolism in fld mice reveal a role for lipin 1 in regulating VLDL-triacylglyceride secretion;Chen;Arterioscler. Thromb. Vasc. Biol.,2008

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