Bone marrow stem cells contribute to repair of the ischemically injured renal tubule

被引:404
作者
Kale, S
Karihaloo, A
Clark, PR
Kashgarian, M
Krause, DS
Cantley, LG
机构
[1] Yale Univ, Sch Med, Nephrol Sect, New Haven, CT 06437 USA
[2] Yale Univ, Sch Med, Dept Lab Med, New Haven, CT 06437 USA
[3] Yale Univ, Sch Med, Dept Pathol, New Haven, CT 06437 USA
关键词
D O I
10.1172/JCI200317856
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The paradigm for recovery of the renal tubule from acute tubular necrosis is that surviving cells from the areas bordering the injury must migrate into the regions of tubular denudation and proliferate to re-establish the normal tubular epithelium. However, therapies aimed at stimulating these events have failed to alter the course of acute renal failure in human trials. In the present study, we demonstrate that Lin(-)Sca-1(+) cells from the adult mouse bone marrow are mobilized into the circulation by transient renal ischemia and home specifically to injured regions of the renal tubule. There they differentiate into renal tubular epithelial cells and appear to constitute the majority of the cells present in the previously necrotic tubules. Loss of stem cells following bone marrow ablation results in a greater rise in blood urea nitrogen after renal ischemia, while stem cell infusion after bone marrow ablation reverses this effect. Thus, therapies aimed at enhancing the mobilization, propagation, and/or delivery of bone marrow stem cells to the kidney hold potential as entirely new approaches for the treatment of acute tubular necrosis.
引用
收藏
页码:42 / 49
页数:8
相关论文
共 28 条
[21]  
SHANLEY PF, 1986, AM J PATHOL, V122, P462
[22]   PURIFICATION AND CHARACTERIZATION OF MOUSE HEMATOPOIETIC STEM-CELLS [J].
SPANGRUDE, GJ ;
HEIMFELD, S ;
WEISSMAN, IL .
SCIENCE, 1988, 241 (4861) :58-62
[23]   Medical progress - Acute renal failure [J].
Thadhani, R ;
Pascual, M ;
Bonventre, JV .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (22) :1448-1460
[24]   Liver from bone marrow in humans [J].
Theise, ND ;
Nimmakayalu, M ;
Gardner, R ;
Illei, PB ;
Morgan, G ;
Teperman, L ;
Henegariu, O ;
Krause, DS .
HEPATOLOGY, 2000, 32 (01) :11-16
[25]  
UCHIDA N, 1994, BLOOD, V83, P3758
[26]   Thresholds for cellular disruption and activation of the stress response in renal epithelia [J].
Van Why, SK ;
Kim, S ;
Geibel, J ;
Seebach, FA ;
Kashgarian, M ;
Siegel, NJ .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1999, 277 (02) :F227-F234
[27]   LOCALIZATION OF PROLIFERATING CELL NUCLEAR ANTIGEN, VIMENTIN, C-FOS, AND CLUSTERIN IN THE POSTISCHEMIC KIDNEY - EVIDENCE FOR A HETEROGENOUS GENETIC RESPONSE AMONG NEPHRON SEGMENTS, AND A LARGE POOL OF MITOTICALLY ACTIVE AND DEDIFFERENTIATED CELLS [J].
WITZGALL, R ;
BROWN, D ;
SCHWARZ, C ;
BONVENTRE, JV .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (05) :2175-2188
[28]   Disruption of overlapping transcripts in the ROSA beta geo 26 gene trap strain leads to widespread expression of beta-galactosidase in mouse embryos and hematopoietic cells [J].
Zambrowicz, BP ;
Imamoto, A ;
Fiering, S ;
Herzenberg, LA ;
Kerr, WG ;
Soriano, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (08) :3789-3794