FGF-1 induces expression of LXRα and production of 25-hydroxycholesterol to upregulate the apoE gene in rat astrocytes

被引:15
|
作者
Lu, Rui [1 ]
Ito, Jinichi [1 ]
Iwamoto, Noriyuki [1 ]
Nishimaki-Mogami, Tomoko [2 ]
Yokoyama, Shinji [1 ]
机构
[1] Nagoya City Univ, Sch Med Sci, Dept Biochem, Nagoya, Aichi 4678601, Japan
[2] Natl Inst Hlth Sci, Dept Biochem & Metab, Tokyo 1588501, Japan
基金
日本学术振兴会;
关键词
high density lipoprotein; cholesterol; direct repeat 4; LIVER-X-RECEPTOR; APOLIPOPROTEIN-E GENE; HIGH-DENSITY-LIPOPROTEIN; CENTRAL-NERVOUS-SYSTEM; CHOLESTEROL HOMEOSTASIS; CELLULAR CHOLESTEROL; GROWTH-FACTORS; MACROPHAGES; SECRETION; HDL;
D O I
10.1194/jlr.M800594-JLR200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fibroblast growth factor 1 (FGF-1) enhances apolipoprotein E (apoE) expression and apoE-HDL biogenesis in autocrine fashion in astrocytes (Ito, J., Y. Nagayasu, R. Lu, A. Kheirollah, M. Hayashi, and S. Yokoyama. Astrocytes produce and secrete FGF-1, which promotes the production of apoE-HDL in a manner of autocrine action. J. Lipid Res. 2005. 46: 679-686) associated with healing of brain injury (Tada, T., J-i. Ito, M. Asai, and S. Yokoyama. Fibroblast growth factor 1 is produced prior to apolipoprotein E in the astrocytes after cryo-injury of mouse brain. Neurochem. Int. 2004. 45: 23-30). FGF-1 stimulates mitogen-activated protein kinase kinase/extracellular signal-regulated kinase (MEK/ERK) to increase cholesterol biosynthesis and phosphatidylinositol 3-OH kinase (PI3K)/Akt to enhance apoEHDL secretion (Ito, J., Y. Nagayasu, K. Okumura-Noji, R. Lu, T. Nishida, Y. Miura, K. Asai, A. Kheirollah, S. Nakaya, and S. Yokoyama. Mechanism for FGF-1 to regulate biogenesis of apoE-HDL in astrocytes. J. Lipid Res. 2007. 48: 2020-2027). We investigated the mechanism for FGF-1 to upregulate apoE transcription. FGF-1 increased apoE and liver X receptor alpha (LXR alpha) mRNAs in rat astrocytes. Increase of LXR alpha mRNA was suppressed by inhibition of the FGF-1 receptor-1 and MEK/ERK but not by inhibition of PI3K/Akt. The increases of apoE mRNA and apoE-HDL secretion were both inhibited by downregulation or inhibition of LXR alpha, while they were partially suppressed by inhibiting cholesterol biosynthesis. We identified the liver X receptor element responsible for activation of the rat apoE promoter by FGF-1 located between 2450 and 2320 bp, and the direct repeat 4 (DR4) element in this region (2448 to 2433 bp) was responsible for the activation. Chromatin immunoprecipitation analysis supported that FGF-1 enhanced association of LXR with the rat apoE promoter. FGF-1 partially activated the apoE promoter even in the presence of an MEK inhibitor that inhibits the FGF-1-mediated enhancement of cholesterol biosynthesis. On the other hand, FGF-1 induced production of 25-hydroxycholesterol by MEK/ERK as an sterol regulatory element-dependent reaction besides cholesterol biosynthesis. We concluded that FGF-1-induced apoE expression in astrocytes depends on LXR alpha being mediated by both LXRa expression and an LXR alpha ligand biosynthesis.-Lu, R., J. Ito, N. Iwamoto, T. Nishimaki-Mogami, and S. Yokoyama. FGF-1 induces expression of LXRa and production of 25-hydroxycholesterol to upregulate the apoE gene in rat astrocytes. J. Lipid Res. 2009. 50: 1156-1164.
引用
收藏
页码:1156 / 1164
页数:9
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