Gene expression profile in the regenerating rat liver after partial hepatectomy

被引:88
作者
Fukuhara, Y
Hirasawa, A
Li, XK
Kawasaki, M
Fujino, M
Funeshima, N
Katsuma, S
Shiojima, S
Yamada, M
Okuyama, T
Suzuki, S
Tsujimoto, G
机构
[1] Natl Res Inst Child Hlth & Dev, Dept Mol Cell Pharmacol, Setagaya Ku, Tokyo 1548567, Japan
[2] Keio Univ, Sch Med, Dept Pediat, Tokyo, Japan
[3] Natl Res Inst Child Hlth & Dev, Dept Innovat Surg, Setagaya Ku, Tokyo 1548567, Japan
基金
日本科学技术振兴机构;
关键词
complementary DNA microarray; liver regeneration; hepatectomy; clustering analysis;
D O I
10.1016/S0168-8278(03)00077-1
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: When a loss of hepatic mass occurs, the expression of a large number of genes is either induced or altered, accompanying hepatocyte proliferation. In the present study, we made an in-house cDNA microarray containing 4608 elements (Liver chip), and analyzed extensively gene expression profiles of the regenerating liver after 70% partial hepatectomy (PHx) in rats. Methods: RNAs were prepared from three rat livers at each time point (taken at 0, 6, 12, 18, 24, 48, 72 h, and I week after PHx). Using the liver chip, we performed large-scale analysis of gene expression during liver regeneration. Elements either up- or down-regulated more than twofold at one or more time points were selected. Results: Among the 4608, 382 were identified. Using cluster analysis, we found great similarity between gene-expression profiles at 12 and 18 h after PHx as well as between 48 and 72 h after PHx. We also found that there are at least six distinct temporal patterns of gene expression in the regenerating rat liver after PHx. Conclusions: These results indicated that microarray analysis is a powerful approach for monitoring molecular events in the regenerating liver. (C) 2003 European Association for the Study of the Liver. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:784 / 792
页数:9
相关论文
共 27 条
[1]   INFLUENCE OF TRANSCRIPTIONAL REGULATION AND MESSENGER-RNA STABILITY ON HEMOPEXIN GENE-EXPRESSION IN REGENERATING LIVER [J].
ALBRECHT, JH ;
MULLEREBERHARD, U ;
KREN, BT ;
STEER, CJ .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1994, 314 (01) :229-233
[2]   LIVER-REGENERATION - A COMPARISON OF IN-SITU HYBRIDIZATION FOR HISTONE MESSENGER-RNA WITH BROMODEOXYURIDINE LABELING FOR THE DETECTION OF S-PHASE CELLS [J].
ALISON, M ;
CHAUDRY, Z ;
BAKER, J ;
LAUDER, I ;
PRINGLE, H .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1994, 42 (12) :1603-1608
[3]  
BAUMANN H, 1993, J IMMUNOL, V151, P4248
[4]   Normalization and subtraction: Two approaches to facilitate gene discovery [J].
Bonaldo, MDF ;
Lennon, G ;
Soares, MB .
GENOME RESEARCH, 1996, 6 (09) :791-806
[5]   TRANSCRIPTION FACTORS MODULATING ANGIOTENSINOGEN GENE-EXPRESSION IN HEPATOCYTES [J].
BRASIER, AR ;
LI, JY ;
COPLAND, A .
KIDNEY INTERNATIONAL, 1994, 46 (06) :1564-1566
[6]   Hepatic and extra-hepatic transcription of inter-α-inhibitor family genes under normal or acute inflammatory conditions in rat [J].
Daveau, M ;
Jean, L ;
Soury, E ;
Olivier, E ;
Masson, S ;
Lyoumi, S ;
Chan, P ;
Hiron, M ;
Lebreton, JP ;
Husson, A ;
Jegou, S ;
Vaudry, H ;
Salier, JP .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1998, 350 (02) :315-323
[7]   DIFFERENT EXPRESSION OF TYROSINE AMINOTRANSFERASE AND SERINE DEHYDRATASE IN RAT LIVERS AFTER PARTIAL-HEPATECTOMY [J].
DELLAFAZIA, MA ;
SERVILLO, G ;
VIOLAMAGNI, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 182 (02) :753-759
[8]   Alcohol dehydrogenase as a critical mediator of retinoic acid synthesis from vitamin A in the mouse embryo [J].
Duester, G .
JOURNAL OF NUTRITION, 1998, 128 (02) :459S-462S
[9]  
Dumontet C, 1996, CELL MOTIL CYTOSKEL, V35, P49, DOI 10.1002/(SICI)1097-0169(1996)35:1<49::AID-CM4>3.0.CO
[10]  
2-D