Comprehensive analysis of differential gene expression profiles on D-galactosamine-induced acute mouse liver injury and regeneration

被引:16
作者
Chung, Heekyoung
Kim, Hyun-Jun
Jang, Ki-Seok
Kim, Mingoo
Yang, Jungeun
Kang, Kyung-Sun
Kim, Hyung-Lae
Yoon, Byung-Il
Lee, Mi-Ock
Lee, Byung-Hoon
Kim, Ju Han
Lee, Yong-Sung
Kong, Gu
机构
[1] Hanyang Univ, Coll Med, Dept Pathol, Seoul 133791, South Korea
[2] Hanyang Univ, TGRC, Seoul 133791, South Korea
[3] Seoul Natl Univ, Coll Med, SNUBI, Seoul 110799, South Korea
[4] Hanyang Univ, Coll Med, Dept Biochem, Seoul 133791, South Korea
[5] Seoul Natl Univ, Coll Vet Med, Dept Vet Publ Hlth, Seoul 151742, South Korea
[6] Seoul Natl Univ, Coll Pharm, Seoul 151742, South Korea
[7] Seoul Natl Univ, Bio MAX Inst, Seoul 151742, South Korea
[8] Seoul Natl Univ, Pharmaceut Sci Res Inst, Seoul 151742, South Korea
[9] Ewha Womans Univ, Coll Med, Dept Biochem, Seoul 158710, South Korea
[10] Kangweon Natl Univ, Sch Vet Med, Chunchon 200701, South Korea
关键词
D-galactosamine (GalN); mouse; liver; toxicogenomics; applied biosystems mouse genome survey microarray;
D O I
10.1016/j.tox.2006.07.026
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Microarray analysis of RNA from D-galactosamine (GalN)-administered mouse livers was performed to establish a global gene expression profile-during injury and regeneration stages at two different doses. A single dose of GalN at 266 or 26.6 mg/kg body weight was given intraperitoneally, and the liver samples were obtained after 6, 24, and 72 h. Histopathologic studies enabled the classification of the D-galactosamine effect into injury (6, 24 h) and regeneration (72 h) stages. By using the Applied Biosystems mouse genome survey microarray, a total of 7267 out of 33,315 (21.8%) genes were found to be statistically reliable at p < 0.05 by two-way ANOVA, and 1469 (4.4%) probes at false discovery rate < 5% by significance analysis of microarray. Among the statistically reliable clones by both analytical methods, 389 genes were differentially expressed when compared with non-treated control, with more than a 1.625-fold difference (which equals 0.7 in 1092 scale) at one or more GalN treatment conditions and with less than 1.625-fold difference at all three vehicle-treated conditions. Three hundred thirty six genes and 13 genes were identified as injury- and regeneration-specific genes, respectively, showing that most of the transcriptomic changes were seen during the injury stage. Furthermore, multiple genes involved in protein synthesis and degradation, mRNA processing and binding, and cell cycle regulation showed variable transcript levels upon acute GalN administration. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:136 / 144
页数:9
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