Mechanism of liver regeneration after partial hepatectomy using mouse cDNA microarray

被引:51
作者
Togo, S
Makino, H
Kobayashi, T
Morita, T
Shimizu, T
Kubota, T
Ichikawa, Y
Ishikawa, T
Okazaki, Y
Hayashizaki, Y
Shimada, H
机构
[1] Yokohama City Univ, Sch Med, Dept Surg 2, Kanazawa Ku, Yokohama, Kanagawa 2360004, Japan
[2] RIKEN, Lab Genome Explorat Res Grp, Genomic Sci Ctr, Yokohama, Kanagawa, Japan
关键词
Liver regeneration; cDNA microarray; partial hepatectomy;
D O I
10.1016/j.jhep.2003.11.005
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: The liver has the capacity to regenerate after partial hepatectomy. In order to clarify the mechanism of liver regeneration, we observed the initial stage, especially the mechanism of gene expression during progress from GO to S phase (0-24 h), and attempted to identify new genes controlling progress to the S phase. Methods: We applied large-scale gene expression analysis with complementary DNA microarrays in mouse hepatectomy models to clarify the mechanism of liver regeneration after partial hepatectomy. Results: As a result, 23 new immediate-early gene candidates such as interleukin-1 receptor associated kinase-1 and karyopherin alpha-1, which are involved in transportation within the nucleus, were discovered. Candidates for new genes concerned with the progress to the S phase were discovered: inhibitor of DNA binding 2 (ID2) and inhibitor of DNA binding 3 (ID3), both new liver regeneration factors that promoted progress to the S phase, and GADD45 gamma (growth arrest and DNA-damage-inducible protein) as a factor inhibiting that process. Conclusions: The above results not only suggest the importance of NFkappaB in the initial stage of liver regeneration but also points to the orderly maintenance of the proliferation of the cells in liver regeneration. (C) 2003 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:464 / 471
页数:8
相关论文
共 23 条
  • [1] THE PROTEIN ID - A NEGATIVE REGULATOR OF HELIX-LOOP-HELIX DNA-BINDING PROTEINS
    BENEZRA, R
    DAVIS, RL
    LOCKSHON, D
    TURNER, DL
    WEINTRAUB, H
    [J]. CELL, 1990, 61 (01) : 49 - 59
  • [2] High-efficiency full-length cDNA cloning by biotinylated CAP trapper
    Carninci, P
    Kvam, C
    Kitamura, A
    Ohsumi, T
    Okazaki, Y
    Itoh, M
    Kamiya, M
    Shibata, K
    Sasaki, N
    Izawa, M
    Muramatsu, M
    Hayashizaki, Y
    Schneider, C
    [J]. GENOMICS, 1996, 37 (03) : 327 - 336
  • [3] Liver regeneration
    Fausto, N
    [J]. JOURNAL OF HEPATOLOGY, 2000, 32 : 19 - 31
  • [4] FITZGERALD MJ, 1995, CELL GROWTH DIFFER, V6, P417
  • [5] Protein kinesis - Nucleocytoplasmic transport
    Gorlich, D
    Mattaj, IW
    [J]. SCIENCE, 1996, 271 (5255) : 1513 - 1518
  • [6] EXPRESSION OF A CELLULAR ONCOGENE DURING LIVER-REGENERATION
    GOYETTE, M
    PETROPOULOS, CJ
    SHANK, PR
    FAUSTO, N
    [J]. SCIENCE, 1983, 219 (4584) : 510 - 512
  • [7] INDUCTION-PATTERNS OF 70 GENES DURING 9 DAYS AFTER HEPATECTOMY DEFINE THE TEMPORAL COURSE OF LIVER-REGENERATION
    HABER, BA
    MOHN, KL
    DIAMOND, RH
    TAUB, R
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (04) : 1319 - 1326
  • [8] HARA E, 1994, J BIOL CHEM, V269, P2139
  • [9] Higgins GM, 1931, ARCH PATHOL, V12, P186
  • [10] Preprocessing implementation for microarray (PRIM): an efficient method for processing cDNA microarray data
    Kadota, K
    Miki, R
    Bono, H
    Shimizu, K
    Okazaki, Y
    Hayashizaki, Y
    [J]. PHYSIOLOGICAL GENOMICS, 2001, 4 (03) : 183 - 188