Mig-6 plays a critical role in the regulation of cholesterol homeostasis and bile acid synthesis.
The disruption of cholesterol homeostasis leads to an increase in cholesterol levels which results in the development of cardiovascular disease. Mitogen Inducible Gene 6 (Mig-6) is an immediate early response gene that can be induced by various mitogens, stresses, and hormones. To identify the metab...
Main Authors: | , , , , , , , , , , |
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Format: | Article |
Language: | English |
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Public Library of Science (PLoS)
2012-01-01
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Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC3422237?pdf=render |
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author | Bon Jeong Ku Tae Hoon Kim Jae Hee Lee Eric D Buras Lisa D White Robert D Stevens Olga R Ilkayeva James R Bain Christopher B Newgard Francesco J DeMayo Jae-Wook Jeong |
author_facet | Bon Jeong Ku Tae Hoon Kim Jae Hee Lee Eric D Buras Lisa D White Robert D Stevens Olga R Ilkayeva James R Bain Christopher B Newgard Francesco J DeMayo Jae-Wook Jeong |
author_sort | Bon Jeong Ku |
collection | DOAJ |
description | The disruption of cholesterol homeostasis leads to an increase in cholesterol levels which results in the development of cardiovascular disease. Mitogen Inducible Gene 6 (Mig-6) is an immediate early response gene that can be induced by various mitogens, stresses, and hormones. To identify the metabolic role of Mig-6 in the liver, we conditionally ablated Mig-6 in the liver using the Albumin-Cre mouse model (Alb(cre/+)Mig-6(f/f); Mig-6(d/d)). Mig-6(d/d) mice exhibit hepatomegaly and fatty liver. Serum levels of total, LDL, and HDL cholesterol and hepatic lipid were significantly increased in the Mig-6(d/d) mice. The daily excretion of fecal bile acids was significantly decreased in the Mig-6(d/d) mice. DNA microarray analysis of mRNA isolated from the livers of these mice showed alterations in genes that regulate lipid metabolism, bile acid, and cholesterol synthesis, while the expression of genes that regulate biliary excretion of bile acid and triglyceride synthesis showed no difference in the Mig-6(d/d) mice compared to Mig-6(f/f) controls. These results indicate that Mig-6 plays an important role in cholesterol homeostasis and bile acid synthesis. Mice with liver specific conditional ablation of Mig-6 develop hepatomegaly and increased intrahepatic lipid and provide a novel model system to investigate the genetic and molecular events involved in the regulation of cholesterol homeostasis and bile acid synthesis. Defining the molecular mechanisms by which Mig-6 regulates cholesterol homeostasis will provide new insights into the development of more effective ways for the treatment and prevention of cardiovascular disease. |
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issn | 1932-6203 |
language | English |
last_indexed | 2024-12-21T06:40:08Z |
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spelling | doaj.art-0e6359e405594a9ba2f1da5581cf38fe2022-12-21T19:12:44ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0178e4291510.1371/journal.pone.0042915Mig-6 plays a critical role in the regulation of cholesterol homeostasis and bile acid synthesis.Bon Jeong KuTae Hoon KimJae Hee LeeEric D BurasLisa D WhiteRobert D StevensOlga R IlkayevaJames R BainChristopher B NewgardFrancesco J DeMayoJae-Wook JeongThe disruption of cholesterol homeostasis leads to an increase in cholesterol levels which results in the development of cardiovascular disease. Mitogen Inducible Gene 6 (Mig-6) is an immediate early response gene that can be induced by various mitogens, stresses, and hormones. To identify the metabolic role of Mig-6 in the liver, we conditionally ablated Mig-6 in the liver using the Albumin-Cre mouse model (Alb(cre/+)Mig-6(f/f); Mig-6(d/d)). Mig-6(d/d) mice exhibit hepatomegaly and fatty liver. Serum levels of total, LDL, and HDL cholesterol and hepatic lipid were significantly increased in the Mig-6(d/d) mice. The daily excretion of fecal bile acids was significantly decreased in the Mig-6(d/d) mice. DNA microarray analysis of mRNA isolated from the livers of these mice showed alterations in genes that regulate lipid metabolism, bile acid, and cholesterol synthesis, while the expression of genes that regulate biliary excretion of bile acid and triglyceride synthesis showed no difference in the Mig-6(d/d) mice compared to Mig-6(f/f) controls. These results indicate that Mig-6 plays an important role in cholesterol homeostasis and bile acid synthesis. Mice with liver specific conditional ablation of Mig-6 develop hepatomegaly and increased intrahepatic lipid and provide a novel model system to investigate the genetic and molecular events involved in the regulation of cholesterol homeostasis and bile acid synthesis. Defining the molecular mechanisms by which Mig-6 regulates cholesterol homeostasis will provide new insights into the development of more effective ways for the treatment and prevention of cardiovascular disease.http://europepmc.org/articles/PMC3422237?pdf=render |
spellingShingle | Bon Jeong Ku Tae Hoon Kim Jae Hee Lee Eric D Buras Lisa D White Robert D Stevens Olga R Ilkayeva James R Bain Christopher B Newgard Francesco J DeMayo Jae-Wook Jeong Mig-6 plays a critical role in the regulation of cholesterol homeostasis and bile acid synthesis. PLoS ONE |
title | Mig-6 plays a critical role in the regulation of cholesterol homeostasis and bile acid synthesis. |
title_full | Mig-6 plays a critical role in the regulation of cholesterol homeostasis and bile acid synthesis. |
title_fullStr | Mig-6 plays a critical role in the regulation of cholesterol homeostasis and bile acid synthesis. |
title_full_unstemmed | Mig-6 plays a critical role in the regulation of cholesterol homeostasis and bile acid synthesis. |
title_short | Mig-6 plays a critical role in the regulation of cholesterol homeostasis and bile acid synthesis. |
title_sort | mig 6 plays a critical role in the regulation of cholesterol homeostasis and bile acid synthesis |
url | http://europepmc.org/articles/PMC3422237?pdf=render |
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