Global analysis of gene expression in renal ischemia-reperfusion in the mouse

被引:40
|
作者
Yoshida, T
Tang, SS
Hsiao, LL
Jensen, RV
Ingelfinger, JR
Gullans, SR
机构
[1] Brigham & Womens Hosp, Dept Med, Div Renal, Cambridge, MA 02139 USA
[2] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Pediat Nephrol Unit, Boston, MA USA
[3] Wesleyan Univ, Dept Phys, Middletown, CT 06459 USA
关键词
microarray; ischemia reperfusion; renal failure; extracellular matrix; tissue repair;
D O I
10.1006/bbrc.2002.6535
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
Ischemia-induced acute renal failure (ARF) is a relatively common disorder with major morbidity and mortality. To study global gene expression during ARF, 6-week-old C57BL/6 male mice underwent 30 min of bilateral renal ischemia followed by reperfusion [I/R] or sham operation. Oligonucleotide microarrays [Affymetrix] with approximately 10,000 genes, 6,643 of which were present in mouse kidney, were used to analyze mRNA expression for up to 4 days following I/R. Fifty-two genes at day 1 and 40 at day 4 were up-regulated more than 4-fold [400%]. Seventy genes at day 1 and 30 genes at day 4 were down-regulated to under 0.25-fold from baseline [25%]. Real-time quantitative RT-PCR confirmed changes in expression for 8 genes of interest. Most of the induced transcripts are involved in cell structure, extracellular matrix, intracellular calcium binding, and cell division/differentiation. Our data identified several novel genes that may be important in renal repair after ischemia. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:787 / 794
页数:8
相关论文
共 50 条
  • [21] Complement and renal ischemia-reperfusion injury
    Bonventre, JV
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 2001, 38 (02) : 430 - 433
  • [22] Ischemia-Reperfusion Increases TRPM7 Expression in Mouse Retinas
    Martinez-Gil, Natalia
    Kutsyr, Oksana
    Fernandez-Sanchez, Laura
    Sanchez-Saez, Xavier
    Albertos-Arranz, Henar
    Sanchez-Castillo, Carla
    Vidal-Gil, Lorena
    Cuenca, Nicolas
    Lax, Pedro
    Maneu, Victoria
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2023, 24 (22)
  • [23] BacMam Delivery of a Protective Gene to Reduce Renal Ischemia-Reperfusion Injury
    Hitchman, Elisabetta
    Hitchman, Richard B.
    King, Linda A.
    [J]. HUMAN GENE THERAPY, 2017, 28 (09) : 747 - 756
  • [24] CD44 expression in renal ischemia-reperfusion injury in rats
    Kocak, Burak
    Orug, Taner
    Turhan, Nesrin
    Ozcay, Necdet
    Gonenc, Faruk
    [J]. INTERNATIONAL UROLOGY AND NEPHROLOGY, 2009, 41 (04) : 791 - 794
  • [25] CD44 expression in renal ischemia-reperfusion injury in rats
    Burak Kocak
    Taner Orug
    Nesrin Turhan
    Necdet Ozcay
    Faruk Gonenc
    [J]. International Urology and Nephrology, 2009, 41 : 791 - 794
  • [26] Weighted Gene Coexpression Network Analysis in Mouse Livers following Ischemia-Reperfusion and Extensive Hepatectomy
    Liu, Wei
    Shi, Yongquan
    Cheng, Tao
    Jia, Ruixue
    Sun, Ming-Zhong
    Liu, Shuqing
    Liu, Qinlong
    [J]. EVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE, 2021, 2021
  • [27] EFFECT OF RENAL ISCHEMIA-REPERFUSION ON EXPRESSION OF THE RENIN-ANGIOTENSIN SYSTEM
    KONTOGIANNIS, J
    WEHBI, G
    WANG, YH
    BURNS, KD
    [J]. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 1995, 6 (03): : 983 - 983
  • [28] Expression and effect of Pbrm1 in renal ischemia-reperfusion injury
    Tian, Puxun
    Gao, Yang
    Wei, Tian
    Zhang, Xingzhe
    Dou, Meng
    Zheng, Bingxuan
    Niu, Zejiaxin
    Deng, Ge
    [J]. TRANSPLANTATION, 2024, 108 (09) : 477 - 477
  • [29] Expression analysis of long non-coding RNAs in a renal ischemia-reperfusion injury model
    Qiu Tao
    Wang Tianyu
    Zhou Jiangqiao
    Chen Zhongbao
    Ma Xiaoxiong
    Zhang Long
    Zou Jilin
    [J]. ACTA CIRURGICA BRASILEIRA, 2019, 34 (04)
  • [30] KIDNEY-CENTERED RADIOTHERAPY ATTENUATES RENAL ISCHEMIA-REPERFUSION INJURY IN MOUSE
    Khbouz, B.
    Rowart, P.
    Krzesinski, J. M.
    Lallemand, F.
    Jouret, F.
    [J]. TRANSPLANT INTERNATIONAL, 2020, 33 : 9 - 9