Differential expressions of lipid metabolism related genes in the liver of young apoE knockout mice.
- Author:
Hong-Yan YE
1
;
Miao YIN
;
Yun-Ju SHANG
;
Xue-Dong DAI
;
Sheng-Qiang ZHANG
;
Wen JING
;
Hui-Qin DU
;
Liang ZHANG
;
Jie PAN
Author Information
1. The Key Laboratory of Animal Resistant Biology of Shandong Province, College of Life Sciences, Shandong Normal University, Jinan 250014, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Apolipoprotein A-I;
metabolism;
Apolipoprotein B-100;
blood;
Apolipoproteins A;
metabolism;
Apolipoproteins E;
genetics;
Atherosclerosis;
genetics;
Gene Expression;
Lipid Metabolism;
genetics;
Lipoproteins, HDL;
blood;
Lipoproteins, LDL;
blood;
Liver;
metabolism;
Mice;
Mice, Knockout;
Triglycerides;
blood
- From:
Acta Physiologica Sinica
2008;60(1):51-58
- CountryChina
- Language:Chinese
-
Abstract:
The work was aimed to investigate the differential expressions of lipid metabolism related genes in the early stage of atherosclerosis in the young apolipoprotein E deficient (apoE(-/-)) mice at different ages with normal chow diet. The genotypes of mice were identified by using multiplex polymerase chain reaction (multi-PCR) analysis. The semi-quantitative reverse transcription-polymerase chain reaction (RT-PCR) and real-time quantitative RT-PCR were used to analyze the expressions of lipid metabolism related genes in the liver of apoE(-/-) and age-matched wild type (WT) mice of 14-day old, 1-month old, 2-month old, 3-month old. The serum total cholesterol (TC), triglyceride (TG), low-density lipoprotein cholesterol (LDL-C) and high-density lipoprotein cholesterol (HDL-C) contents were assayed using COD-PAP and GPO-PAP methods. The serum apolipoprotein B100 (apoB100) content was quantitated by immune turbidimetry. The hearts were perfusion-fixed in 4% formaldehyde, infiltrated with 30% gum sucrose for 24 h at 4 °C, and embedded in OCT compound. The aortic sinus tissues were serially sectioned at -15 °C, stained with Sudan IV, and counterstained with light green. The results were shown as follows. Compared with that in WT mice, the mRNA levels of apoA I and apoA IV in apoE(-/-) mice aged from 14-day old to 3-month old changed prominently (P<0.05), with apoA I up-regulated and apoA IV down-regulated. At the age of 1 month, the expression of apoB100 in apoE(-/-) mice was higher than that in WT mice (P<0.05). The expression of apoA V was up-regulated (P<0.05) and there was obvious lipid deposition in the aortic intima in apoE(-/-) mice at the age of 2 months. The expressions of fatty acid translocase (Fat/CD36) and angiopoietin-like protein 3 (Angptl 3) in apoE(-/-) mice were higher than those in WT mice at the age of 3 months (P<0.05), while the expressions of peroxisome proliferator-activated receptor α (PPARα), liver X receptor α (LXRα), carnitine palmitoyl transferase I (CPT I) and acyl coenzyme A oxidase 1 (ACOX1) showed no significant changes. The serum TC, TG, LDL-C and HDL-C contents in apoE(-/-) mice aged from 14-day old to 3-month old were higher than those in age-matched WT mice. apoE(-/-) mice showed a marked increase in serum apoB100 content, consistent with the trend of serum LDL-C content and apoB100 mRNA content in the liver. The results suggest that the mRNA expressions of apoA I, apoA IV, apoA V, apoB100 and Angptl 3 in apoE(-/-) mice change significantly compared with those in WT mice, and these genes might be relevant to the complicated lipid metabolism network, and involved in the early stage of atherogenesis.
