Expression of Fc α/μ receptor by human mesangial cells:: A candidate receptor for immune complex deposition in IgA nephropathy

被引:60
作者
McDonald, KJ
Cameron, AJM
Allen, JM
Jardine, AG
机构
[1] Western Infirm & Associated Hosp, Renal Unit, Glasgow G11 6NT, Lanark, Scotland
[2] Univ Glasgow, Western Infirm, Dept Med & Therapeut, Glasgow G11 6NT, Lanark, Scotland
基金
英国惠康基金;
关键词
Fc alpha/mu receptor; IgA nephropathy; mesangial cells; glomerular mesangium; IgA; IgM;
D O I
10.1006/bbrc.2001.6218
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
IgA nephropathy is characterized by the deposition of IgA immune complexes in the glomerular mesangium, but the mechanisms responsible for this are not well understood. Human mesangial cells (HMCs) can bind IgA but do not express known IgA receptors. We show here that primary HMCs express mRNA for a novel receptor, the Fc alpha/mu receptor (Fcalpha/muR), and that receptor expression is upregulated by IL-1. We also detected mRNA for a novel receptor variant in HMCs that may encode a soluble form of the receptor. Fcalpha/muR was expressed in a heterologous system which showed that the receptor was approximately 58 kDa in weight and was only minimally N-glycosylated. As predicted from the characteristics of the murine homologue, the expressed human Fcalpha/muR was able to bind IgA and IgM, but not IgG. These results suggest that Fcalpha/muR may be the receptor responsible for mesangial IgA deposition in IgA nephropathy. (C) 2002 Elsevier Science.
引用
收藏
页码:438 / 442
页数:5
相关论文
共 20 条
[1]   Identification of a novel Fcα receptor expressed by human mesangial cells [J].
Barratt, J ;
Greer, MR ;
Pawluczyk, IZA ;
Allen, AC ;
Bailey, EM ;
Buck, KS ;
Feehally, J .
KIDNEY INTERNATIONAL, 2000, 57 (05) :1936-1948
[2]   Differential effects of circulating IgA isolated from patients with IgA nephropathy on superoxide and fibronectin production of mesangial cells [J].
Chen, HC ;
Guh, JY ;
Chang, JM ;
Lai, YH .
NEPHRON, 2001, 88 (03) :211-217
[4]   IgA induced activation of human mesangial cells:: Independent of FcαR1 (CD 89) [J].
Diven, SC ;
Caflisch, CR ;
Hammond, DK ;
Weigel, PH ;
Oka, JA ;
Goldblum, RM .
KIDNEY INTERNATIONAL, 1998, 54 (03) :837-847
[5]   Increased dimeric IgA producing B cells in the bone marrow in IgA nephropathy determined by in situ hybridisation for J chain mRNA [J].
Harper, SJ ;
Allen, AC ;
Pringle, JH ;
Feehally, J .
JOURNAL OF CLINICAL PATHOLOGY, 1996, 49 (01) :38-42
[6]   Mass spectrometry proves under-O-glycosylation of glomerular IgA1 in IgA nephropathy [J].
Hiki, Y ;
Odani, H ;
Takahashi, M ;
Yasuda, Y ;
Nishimoto, A ;
Iwase, H ;
Shinzato, T ;
Kobayashi, Y ;
Maeda, K .
KIDNEY INTERNATIONAL, 2001, 59 (03) :1077-1085
[7]   Fcα receptor (CD89) mediates the development of immunoglobulin A (IgA) nephropathy (Berger's disease):: Evidence for pathogenic soluble receptor-IgA complexes in patients and CD89 transgenic mice [J].
Launay, P ;
Grossetête, B ;
Arcos-Fajardo, M ;
Gaudin, E ;
Torres, SP ;
Beaudoin, L ;
de Serre, NPM ;
Lehuen, A ;
Monteiro, RC .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 191 (11) :1999-2009
[8]   ELEVATION OF IGA IN IGA NEPHROPATHY IS LOCALIZED IN THE SERUM AND NOT SALIVA AND IS RESTRICTED TO THE IGA1 SUBCLASS [J].
LAYWARD, L ;
ALLEN, AC ;
HATTERSLEY, JM ;
HARPER, SJ ;
FEEHALLY, J .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 1993, 8 (01) :25-28
[9]  
Leung JCK, 2000, J AM SOC NEPHROL, V11, P241, DOI 10.1681/ASN.V112241
[10]   Charge-dependent binding of polymeric IgA1 to human mesangial cells in IgA nephropathy [J].
Leung, JCK ;
Tang, SCW ;
Lam, MF ;
Chan, TM ;
Lai, KN .
KIDNEY INTERNATIONAL, 2001, 59 (01) :277-285