Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2005 Nov 21:2:33.
doi: 10.1186/1743-7075-2-33.

Phosphoenolpyruvate carboxykinase and the critical role of cataplerosis in the control of hepatic metabolism

Parvin Hakimi  1 , Mark T Johnson, Jianqi Yang, David F Lepage, Ronald A Conlon, Satish C Kalhan, Lea Reshef, Shirley M Tilghman, Richard W Hanson
Affiliations

Phosphoenolpyruvate carboxykinase and the critical role of cataplerosis in the control of hepatic metabolism

Parvin Hakimi et al. Nutr Metab (Lond). .

Abstract

Background: The metabolic function of PEPCK-C is not fully understood; deletion of the gene for the enzyme in mice provides an opportunity to fully assess its function.

Methods: The gene for the cytosolic form of phosphoenolpyruvate carboxykinase (GTP) (EC 4.1.1.32) (PEPCK-C) was deleted in mice by homologous recombination (PEPCK-C-/- mice) and the metabolic consequences assessed.

Results: PEPCK-C-/- mice became severely hypoglycemic by day two after birth and then died with profound hypoglycemia (12 mg/dl). The mice had milk in their stomachs at day two after birth and the administration of glucose raised the concentration of blood glucose in the mice but did not result in an increased survival. PEPCK-C-/- mice have two to three times the hepatic triglyceride content as control littermates on the second day after birth. These mice also had an elevation of lactate (2.5 times), beta-hydroxybutyrate (3 times) and triglyceride (50%) in their blood, as compared to control animals. On day two after birth, alanine, glycine, glutamine, glutamate, aspartate and asparagine were elevated in the blood of the PEPCK-C-/- mice and the blood urea nitrogen concentration was increased by 2-fold. The rate of oxidation of [2-14C]-acetate, and [5-14C]-glutamate to 14CO2 by liver slices from PEPCK-C-/- mice at two days of age was greatly reduced, as was the rate of fatty acid synthesis from acetate and glucose. As predicted by the lack of PEPCK-C, the concentration of malate in the livers of the PEPCK-C-/- mice was 10 times that of controls.

Conclusion: We conclude that PEPCK-C is required not only for gluconeogenesis and glyceroneogenesis but also for cataplerosis (i.e. the removal of citric acid cycle anions) and that the failure of this process in the livers of PEPCK-C-/- mice results in a marked reduction in citric acid cycle flux and the shunting of hepatic lipid into triglyceride, resulting in a fatty liver.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Generation of PEPCK-C-/- mice. Panel A. Diagram of the _targeting vector, which is aligned with endogenous sequence of PEPCK-C gene. The sequence between Pst I and Xho I, which covers part of the gene promoter and the exons 1 and 2 in endogenous gene, was replaced with Neo resistance gene (PGK_βgal-neoR) in the _targeting vector. H, Hind III; P, Pst I; X, Xho I. PGK_βgal-neoR, the phosphoglycerate kinase gene promoter drives a fusion gene of βgal and neoR. DTA, the diphtheria toxin A chain. Panel B. Genotyping of the PEPCK-C-/- mice by Southern blotting. Genomic DNA was digested with Hind III and hybridized with a PEPCK-C cDNA probe composed of exons 1~6 of the rat PEPCK-C gene (black bars). For the wild type allele of PEPCK-C, 1.3-kb and 2.75-kb fragments were detected; only one fragment (2.5 kb) was excepted for the _targeted allele.
Figure 2
Figure 2
Characterization of the PEPCK-C-/- mice. Panel A. A representative Northern blot for mRNA isolated from the liver and kidney of two-day-old mice. Panel B. PEPCK-C activity was determined in the livers of two-day-old mice. The results are expressed as the mean ± S.E. for three animals in each group. Panel C. Photograph of two-day-old PEPCK-C-/- mice. Panel D. Growth retardation of PEPCK-C-/- mice. Body weights of neonates were measure at 6, 30, and 37 h after birth. Three wild type mice and three PEPCK-C-/- mice were used.
Figure 3
Figure 3
Alterations in glucose homeostaisis in PEPCK-C-/- and control mice during the perinatal period. Panel A Hypoglycemia in PEPCK-C-/- mice. The concentration of blood glucose was measured in mice at one, two and three days after birth. The results are expressed as the mean ± S.E. for from three to six animals. Panel B. Increased mobilization of hepatic glycogen. The hepatic glycogen level was analyzed at the age of fetal day 19 (day -1) and neonatal day (day +2). The results are expressed as the mean ± S.E. for three animals in each group.
Figure 4
Figure 4
Morphology of the livers of PEPCK-C-/- and control mice. Livers of two-day-old pups were analyzed with H&E staining. The arrow indicates fat accumulation in the liver of PEPCK-C-/- mice.
Figure 5
Figure 5
The concentration of amino acids in the blood of PEPCK-C-/- mice and controls. The levels of amino acids were determined in mice at two days after birth. The results are expressed as the mean ± S.E. of three controls and four PEPCK-C-/- mice.
Figure 6
Figure 6
The role of PEPCK-C in cataplerosis in the liver. The reactions of the citric acid cycle are presented, with the major end-products shown in gold boxes; the large red box represents the mitochondrial membrane. The concentrations of amino acids, β-hydroxybutyrate, glucose and triglyceride were determined from blood samples, while the levels of malate and pyruvate were determined from freeze-clamped liver. The ablation of PEPCK-C (shown by a red bar) results in a 10-fold increase in the concentration of malate in the liver (we did not distinguish between malate in the cytosol and the mitochondria) and a build-up of cycle intermediates [23]. This leads to a decrease in the rate of citric acid cycle flux and the resultant accumulation of acetyl CoA, which is subsequently converted to ketone bodies and released by the liver. The rate of fatty acid oxidation in the PEPCK-C-/- mice is also markedly decreased, resulting in an increase in triglyceride synthesis from these fatty acids that leads to the development of a fatty liver. There is also a marked increase in the concentration of amino acids in the blood that were generated from citric acid cycle intermediates. The increased rate of flux of intermediates leaving the citric acid cycle is denoted by heavy arrows.
See this image and copyright information in PMC

Similar articles

See all similar articles

Cited by

See all "Cited by" articles

References

    1. Chakravarty K, Cassuto H, Reshef L, Hanson RW. Factors that control the tissue-specific transcription of the gene for phosphoenolpyruvate carboxykinase-C. Crit Rev Biochem Mol Biol. 2005;40:129–154. doi: 10.1080/10409230590935479. - DOI - PubMed
    1. Hanson RW, Patel YM. P-enolpyruvate carboxykinase: the gene and the enzyme. In: Meister A, editor. Advances in Enzymology. Vol. 69. New York, John Wiley and Sons; 1994. pp. 203–281. - PubMed
    1. Reshef L, Hanson RW, Ballard FJ. A possible physiological role for glyceroneogenesis in rat adipose tissue. J Biol Chem. 1970;245:5979–5984. - PubMed
    1. Botion LM, Brito MN, Brito NA, Brito SR, Kettelhut IC, Migliorini RH. Glucose contribution to in vivo synthesis of glyceride-glycerol and fatty acids in rats adapted to a high-protein, carbohydrate-free diet. Metabolism. 1998;47:1217–1221. doi: 10.1016/S0026-0495(98)90326-2. - DOI - PubMed
    1. Kalhan SC, Mahajan S, Burkett E, Reshef L, Hanson RW. Glyceroneogenesis and the source of glycerol for hepatic triacylglycerol synthesis in humans. J Biol Chem. 2001;276:12928–12931. doi: 10.1074/jbc.M006186200. - DOI - PubMed
  NODES
admin 1
Note 1
twitter 2