Renal Toll-like receptors: recent advances and implications for disease

被引:48
作者
El-Achkar, Tarek M. [1 ]
Dagher, Pierre C. [1 ]
机构
[1] Indiana Univ, Dept Med, Div Nephrol, Indiana Ctr Biol Microscopy, Indianapolis, IN 46202 USA
来源
NATURE CLINICAL PRACTICE NEPHROLOGY | 2006年 / 2卷 / 10期
关键词
glomerulonephritis; inflammation; ischemia; renal failure; sepsis;
D O I
10.1038/ncpneph0300
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
Toll-like receptors (TLRs) are proteins that recognize specific molecular patterns of pathogens. They can also interact with a variety of endogenous ligands. When stimulated, TLRs initiate a cascade of signaling events leading to the production of a myriad of cytokines and effector molecules. Early investigations extensively characterized TLRs on cells of the innate immune system. More recently, TLRs have been found to reside in organs such as the heart, lungs, intestines, liver and kidneys. The role of these TLRs is not fully understood and is the subject of intensive current research. The available information indicates that renal TLRs have the potential to interact with exogenous and endogenous ligands, thereby influencing kidney function in health and disease. Here, we present an overview of what is currently known about renal TLRs, and discuss the potential implications for further research and clinical practice.
引用
收藏
页码:568 / 581
页数:14
相关论文
共 149 条
[71]   Cyclosporine-induced renal injury induces toll-like receptor and maturation of dendritic cells [J].
Lim, SW ;
Li, C ;
Ahn, KO ;
Kim, J ;
Moon, IS ;
Ahn, C ;
Lee, JR ;
Yang, CW .
TRANSPLANTATION, 2005, 80 (05) :691-699
[72]   Endotoxin and cytokine regulation of toll-like receptor (TLR) 2 and TLR4 gene expression in murine liver and hepatocytes [J].
Matsumura, T ;
Ito, A ;
Takii, T ;
Hayashi, H ;
Onozaki, K .
JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 2000, 20 (10) :915-921
[73]   Cytomegalovirus seromismatching increases the risk of acute renal allograft rejection [J].
McLaughlin, K ;
Wu, C ;
Fick, G ;
Muirhead, N ;
Hollomby, D ;
Jevnikar, A .
TRANSPLANTATION, 2002, 74 (06) :813-816
[74]   Human lupus autoantibody-DNA complexes activate DCs through cooperation of CD32 and TLR9 [J].
Means, TK ;
Latz, E ;
Hayashi, F ;
Murali, MR ;
Golenbock, DT ;
Luster, AD .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (02) :407-417
[75]   A human homologue of the Drosophila Toll protein signals activation of adaptive immunity [J].
Medzhitov, R ;
PrestonHurlburt, P ;
Janeway, CA .
NATURE, 1997, 388 (6640) :394-397
[76]  
MICHIE HR, 1988, SURGERY, V104, P280
[77]  
Morrissey J, 2000, J AM SOC NEPHROL, V11, P1681, DOI 10.1681/ASN.V1191681
[78]   IRAK (Pelle) family member IRAK-2 and MyD88 as proximal mediators of IL-1 signaling [J].
Muzio, M ;
Ni, J ;
Feng, P ;
Dixit, VM .
SCIENCE, 1997, 278 (5343) :1612-1615
[79]   The kinase TAK1 can activate the NIK-IκB as well as the MAP kinase cascade in the IL-1 signalling pathway [J].
Ninomiya-Tsuji, J ;
Kishimoto, K ;
Hiyama, A ;
Inoue, J ;
Cao, ZD ;
Matsumoto, K .
NATURE, 1999, 398 (6724) :252-256
[80]   Tissue-specific mRNA expression profiles of human toll-like receptors and related genes [J].
Nishimura, M ;
Naito, S .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2005, 28 (05) :886-892