Journal of Lipid Research · 2004 · 25 citations · 28 references
Life SciencesBiochemistryMolecular BiologyHepatologyLipid BiochemistryMetabolismFatty Acid MetabolismHepatic PathophysiologyLipid MetabolismLipoprotein MetabolismLiver DiseaseMetabolic Liver DiseaseHepatic Lipid AccumulationHepatic Steatosis AssessmentHepatic Triglyceride MetabolismHigh-density Lipoprotein MetabolismSteatosis BiomarkersSteatosis Quantification
The inbred HcB19 mouse strain expresses a truncated form of thioredoxin interacting protein and is phenotypically characterized by fatty liver and elevated plasma triglycerides and VLDL. Recently, these mice have been proposed as an animal model for familial combined hyperlipidemia. The aim of the present study was identification of hepatic proteins specifically associated with the presence of fatty liver. Eighteen differential proteins were detected in whole-liver homogenate from HcB19, or the parental strain C3H, using 2D electrophoresis, and 11 of those were successfully identified by mass spectrometry. Five of the identified differential proteins were mitochondrial, two peroxisomal, two cytosolic, and two secretory. Four differential proteins were novel in the fatty liver proteome [i.e., aconitase, succinate dehydrogenase, propionyl CoA carboxylase α chain (PCCA), and 3-hydroxyanthranilate and of of in and have identified differential proteins in the hepatic proteome of mice with fatty and and differential of and in of fatty liver or in the of hyperlipidemia. The inbred HcB19 mouse strain expresses a truncated form of thioredoxin interacting protein and is phenotypically characterized by fatty liver and elevated plasma triglycerides and VLDL. Recently, these mice have been proposed as an animal model for familial combined hyperlipidemia. The aim of the present study was identification of hepatic proteins specifically associated with the presence of fatty liver. Eighteen differential proteins were detected in whole-liver homogenate from HcB19, or the parental strain C3H, using 2D electrophoresis, and 11 of those were successfully identified by mass spectrometry. Five of the identified differential proteins were mitochondrial, two peroxisomal, two cytosolic, and two secretory. Four differential proteins were novel in the fatty liver proteome [i.e., aconitase, succinate dehydrogenase, propionyl CoA carboxylase α chain (PCCA), and 3-hydroxyanthranilate and of of in and have identified differential proteins in the hepatic proteome of mice with fatty and and differential of and in of fatty liver or in the of hyperlipidemia. as hepatic or is characterized by the of the of in the of fatty liver. hepatic triglycerides of an of the liver in VLDL. been in with liver in familial is by the of hepatic in the liver an for and fatty liver associated with of in a of the from animal is fatty liver in with familial combined of fatty liver in familial combined as as and the in and in the of and fatty liver is a with the of liver or and for a study of from fatty liver by a in the of and and the or or of the a of and a of the from animal in these of in of these or a protein in of proteins as of protein of mice and mice with of the differential of and associated proteins in HcB19 mouse strain is an inbred mouse strain a HcB19 mice phenotypically characterized by elevated plasma of and fatty as as of hepatic and hepatic a for combined in a mouse Recently, the in HcB19 was identified in thioredoxin interacting protein of the combined The a of thioredoxin a of mice have been proposed with a hepatic fatty fatty of the combined a is with a with in of familial combined for of familial combined in and of of familial combined with of The the of is The HcB19 mouse an animal model of fatty liver in with elevated plasma in by with the and with with those combined or was the aim of study proteins in of HcB19 mice the parental the of fatty liver in and the of the in of plasma and mice and mice of were the animal of the a the of plasma and mice were in a was in and of The were the liver was in in and in the of and liver was in in were and the plasma was and were by the of the of and were was in liver of and in liver study of the and of liver were using the protein The 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truncated of the combined of as in HcB19, and the of the and the thioredoxin by the is in HcB19 the is in the of in HcB19 mice in and a of the in the of HcB19 Recently, thioredoxin as a of in with fatty liver with elevated plasma of from fatty liver the and those thioredoxin as a of in with fatty liver the of the and the in a of protein in hepatic or have been of proteins as of protein of mice and mice with of the differential of and associated proteins in The present identified proteins have been in or in the and is of the in the the HcB19 mice in the present these proteins in of 11 proteins in the differential proteome have been associated with of proteins by of of and is of in HcB19 of and in HcB19 of HcB19 were and in of in or and a in HcB19 in HcB19 mice fatty liver hepatic is in the of the the of hepatic in the of and fatty liver thioredoxin as a of in with fatty liver of an in and fatty for the hepatic and the presence of is C3H, the parental strain of the inbred HcB19 a in an 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have been associated with of proteins by of of and is of in HcB19 of and in HcB19 of HcB19 were and in of in or and a in HcB19 in HcB19 mice fatty liver hepatic is in the of the the of hepatic in the of and fatty liver thioredoxin as a of in with fatty liver of an in and fatty for the hepatic and the presence of is C3H, the parental strain of the inbred HcB19 a in an hepatic the in a study of the of a in have plasma and as as of the HcB19 hepatic and differential of proteins associated with from the of in HcB19 differential proteins were and and have been in fatty liver and in these have been associated with and in with succinate and in the of these two is in with the was in the of HcB19 mice of the combined of the novel hepatic proteins identified as differential in in the of fatty liver. is a the of in the of the is the in the of fatty and been mice as as fatty liver in mice carboxylase and by a the present HcB19 mice of mice of in the of HcB19 mice the of in HcB19 mice of the combined the of a in the of in the liver of of fatty in of the of in have a as of by and in and of the and of and a the of fatty liver. and were in HcB19 mice is a as as thioredoxin in and in the of the and a in HcB19 the in HcB19 is a is in and a been the hepatic in of hepatic and a of been in the liver of the in have in combined the and of the of and in with combined or of with in of combined Recently, with fatty liver have or combined of fatty liver in familial combined the in HcB19 the of been in HcB19 mice a for combined in a mouse in a of the hepatic proteins of HcB19 mice with fatty have identified novel differential and with the parental proteins for the of fatty liver with hyperlipidemia. using mice in a of these proteins in hepatic HcB19 mice an inbred mouse strain in a of is truncated of the combined of as in HcB19, and the of the and the thioredoxin by the is in HcB19 the is in the of in HcB19 mice in and a of the in the of HcB19 Recently, thioredoxin as a of in with fatty liver with elevated plasma of from fatty liver the and those thioredoxin as a of in with fatty liver the of the and the in a of protein in hepatic or have been of proteins as of protein of mice and mice with of the differential of and associated proteins in The present identified proteins have been in or in the and is of the in the the HcB19 mice in the present these proteins in Four of 11 proteins in the differential proteome have been associated with of proteins by of of and is of in HcB19 of and in HcB19 of HcB19 were and in of in or and a in HcB19 in HcB19 mice fatty liver hepatic is in the of the the of hepatic in the of and fatty liver thioredoxin as a of in with fatty liver of an in and fatty for the hepatic and the presence of is C3H, the parental strain of the inbred HcB19 a in an hepatic the in a study of the of a in have plasma and as as of the HcB19 hepatic and differential of proteins associated with from the of in HcB19 Four differential proteins were and and have been in fatty liver and in these have been associated with and in with succinate and in the of these two is in with the was in the of HcB19 mice of the combined of the novel hepatic proteins identified as differential in in the of fatty liver. is a the of in the of the is the in the of fatty and been mice as as fatty liver in mice carboxylase and by a the present HcB19 mice of mice of in the of HcB19 mice the of in HcB19 mice of the combined the of a in the of in the liver of of fatty in of the of in have a as of by and in and of the and of and a the of fatty liver. and were in HcB19 mice is a as as thioredoxin in and in the of the and a in HcB19 the in HcB19 is a is in and a been the hepatic in of hepatic and a of been in the liver of the in have in combined the and of the of and in with combined or of with in of combined Recently, with fatty liver have or combined of fatty liver in familial combined the in HcB19 the of been in HcB19 mice a for combined in a mouse in a of the hepatic proteins of HcB19 mice with fatty have identified novel differential and with the parental proteins for the of fatty liver with hyperlipidemia. using mice in a of these proteins in hepatic The of the for the of for the with the HcB19 and mouse for the HcB19 for with the succinate and for 3-hydroxyanthranilate chain chain protein familial combined CoA protein protein protein of propionyl CoA carboxylase α chain succinate thioredoxin thioredoxin interacting protein
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