Leukemia inhibitory factor is involved in tubular regeneration after experimental acute renal failure

被引:51
作者
Yoshino, J [1 ]
Monkawa, T [1 ]
Tsuji, M [1 ]
Hayashi, M [1 ]
Saruta, T [1 ]
机构
[1] Keio Univ, Sch Med, Dept Internal Med, Shinjuku Ku, Tokyo 1608582, Japan
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2003年 / 14卷 / 12期
关键词
D O I
10.1097/01.ASN.0000101180.96787.02
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Leukemia inhibitory factor (LIF) is known to play a crucial role in the conversion of mesenchyme into epithelium during nephrogenesis. This study was carried out to test the hypothesis that LIF and LIF receptor (LIFR) are involved in the renal epithelial regeneration after acute renal failure. First, the authors investigated the spatiotemporal expression of LIF and LIFR in fetal and adult rat kidney. In developing kidney, LIF was expressed in the ureteric buds and LIFR was located in nephrogenic mesenchyme and the ureteric buds; in adult kidney, LIF and LIFR expression was confined to the collecting ducts. Next, the authors examined the expression of LIF and LIFR during the recovery phase after ischemia-reperfusion injury. Real-time PCR analysis revealed that LIF mRNA expression was significantly increased from day I to day 7 after reperfusion and that LIFR mRNA was upregulated from day 4 to day 14. Histologic analysis demonstrated that the increased expression of LIF mRNA and protein was most marked in the outer medulla, especially in the S3 segment of the proximal tubules. To elucidate the mitogenic role of LIF in the regeneration process, cultured rat renal epithelial (NRK 52E) cells were subjected to ATP depletion (an in vitro model of acute renal failure), and LIF expression was found to be enhanced during recovery after ATP depletion. Blockade of endogenous LIF with a neutralizing antibody significantly reduced the cell number and DNA synthesis during the recovery period. These results suggest that LIF participates in the regeneration process after tubular injury.
引用
收藏
页码:3090 / 3101
页数:12
相关论文
共 45 条
[1]   MOLECULAR EVENTS IN THE ORGANIZATION OF RENAL TUBULAR EPITHELIUM - FROM NEPHROGENESIS TO REGENERATION [J].
BACALLAO, R ;
FINE, LG .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 257 (06) :F913-F924
[2]  
BACALLAO R, 1994, J CELL SCI, V107, P3301
[3]   Activins as regulators of branching morphogenesis [J].
Ball, EMA ;
Risbridger, GP .
DEVELOPMENTAL BIOLOGY, 2001, 238 (01) :1-12
[4]   Mesenchymal to epithelial conversion in rat metanephros is induced by LIF [J].
Barasch, J ;
Yang, J ;
Ware, CB ;
Taga, T ;
Yoshida, K ;
Erdjument-Bromage, H ;
Tempst, P ;
Parravicini, E ;
Malach, S ;
Aranoff, T ;
Oliver, JA .
CELL, 1999, 99 (04) :377-386
[5]   Increased transforming growth factor-beta 1 expression in regenerating rat renal tubules following ischemic injury [J].
Basile, DP ;
Rovak, JM ;
Martin, DR ;
Hammerman, MR .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL FLUID AND ELECTROLYTE PHYSIOLOGY, 1996, 270 (03) :F500-F509
[6]  
Bauer S, 2003, J NEUROSCI, V23, P1792
[7]   MECHANISMS OF ISCHEMIC ACUTE-RENAL-FAILURE [J].
BONVENTRE, JV .
KIDNEY INTERNATIONAL, 1993, 43 (05) :1160-1178
[8]  
Bullock SL, 2001, J AM SOC NEPHROL, V12, P515, DOI 10.1681/ASN.V123515
[9]   EPITHELIOID AND FIBROBLASTIC RAT-KIDNEY CELL CLONES - EPIDERMAL GROWTH-FACTOR (EGF) RECEPTORS AND EFFECT OF MOUSE SARCOMA-VIRUS TRANSFORMATION [J].
DELARCO, JE ;
TODARO, GJ .
JOURNAL OF CELLULAR PHYSIOLOGY, 1978, 94 (03) :335-342
[10]   DEREGULATION OF PAX-2 EXPRESSION IN TRANSGENIC MICE GENERATES SEVERE KIDNEY ABNORMALITIES [J].
DRESSLER, GR ;
WILKINSON, JE ;
ROTHENPIELER, UW ;
PATTERSON, LT ;
WILLIAMSSIMONS, L ;
WESTPHAL, H .
NATURE, 1993, 362 (6415) :65-67