Neutrophil gelatinase-associated lipocalin-mediated iron traffic in kidney epithelia

被引:217
作者
Schmidt-Ott, Kai M.
Mori, Kiyoshi
Kalandadze, Avtandil
Li, Jau-Yi
Paragas, Neal
Nicholas, Thomas
Devarajan, Prasad
Barasch, Jonathan
机构
[1] Columbia Univ Coll Phys & Surg, Dept Med, New York, NY 10032 USA
[2] Kyoto Univ, Grad Sch Med, Dept Med & Clin Sci, Kyoto, Japan
[3] Univ Cincinnati, Coll Med, Cincinnati Childrens Hosp Med Ctr, Div Nephrol & Hypertens, Cincinnati, OH USA
关键词
benzoic acid; enterochelin; neutrophil gelatinase-associated lipocalin; iron; ischemia-reperfusion; kidney; lipocalin; mesenchyme; siderophore; 2,3 dihydroxybenzoic acid;
D O I
10.1097/01.mnh.0000232886.81142.58
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
Purpose of review Neutrophil gelatinase-associated lipocalin (NGAL) is a member of the lipocalin superfamily of carrier proteins. NGAL is the first known mammalian protein which specifically binds organic molecules called siderophores, which are high-affinity iron chelators. Here, we review the expression, siderophore-dependent biological activities and clinical significance of NGAL in epithelial development and in kidney disease. Recent findings NGAL expression is rapidly induced in the nephron in response to renal epithelial injury. This has led to the establishment of NGAL assays that detect renal damage in the human. Additionally, only when complexed with siderophore and iron as a trimer, NGAL induces mesenchymal-epithelial transition (or nephron formation) in embryonic kidney in vitro and protects adult kidney from ischemia-reperfusion injury in vivo. While the structure of the NGAL : siderophore : iron complex has thus far only been solved for bacterially synthesized siderophores, new evidence suggests the presence of mammalian siderophore-like molecules. Summary NGAL is rapidly and massively induced in renal epithelial injury and NGAL : siderophore : iron complexes may comprise a physiological renoprotective mechanism. The data have implications for the diagnosis and treatment of acute renal injury.
引用
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页码:442 / 449
页数:8
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