Renal expression of galectin-3 in systemic lupus erythematosus patients with nephritis

被引:55
作者
Kang, E. H. [1 ]
Moon, K. C. [2 ]
Lee, E. Y. [1 ]
Lee, Y. J. [1 ]
Lee, E. B. [1 ]
Ahn, C. [3 ]
Song, Y. W. [1 ]
机构
[1] Seoul Natl Univ Hosp, Dept Internal Med, Div Rheumatol, Seoul 110744, South Korea
[2] Seoul Natl Univ Hosp, Dept Pathol, Seoul 110744, South Korea
[3] Seoul Natl Univ Hosp, Dept Internal Med, Div Nephrol, Seoul 110744, South Korea
关键词
galectin-3; lupus nephritis; systemic lupus erythematosus; N-TERMINAL DOMAINS; BINDING-PROTEIN; ANIMAL LECTIN; IDENTIFICATION; CELLS; GLOMERULONEPHRITIS; MYOFIBROBLASTS; MACROPHAGES; MONOCYTES; APOPTOSIS;
D O I
10.1177/0961203308094361
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aim of the study is to characterize the expression pattern of galectin-3 (Gal-3) in renal tissues of patients with systemic lupus erythematosus (SLE) nephritis and to determine whether tissue and serum Gal-3 are associated with SLE nephritis. Gal-3 expressions were examined with immunohistochemistry in renal biopsy specimens of 88 patients with SLE nephritis and in five normal specimens. Activity and chronicity indexes and glomerular Gal-3 expressions were analysed in each specimen. Serum Gal-3 levels were measured using enzyme-linked immunosorbent assays in 20 patients with SLE, including I I with nephritis, and in 50 healthy controls. Glomerular Gal-3 expression was observed in 81.8% (72/88) of patients with SLE nephritis but not in 5 controls. Gal-3 staining was attributed mainly to its cellular expression rather than its deposition, and Gal-3 expression levels were correlated with histologic activity indexes, anti-dsDNA titers, and complement 3 and 4 levels. Serum Gal-3 levels were higher in patients with SLE, particularly in those with nephritis, than in healthy controls, and correlated with anti-dsDNA titers. In conclusion, glomerular Gal-3 expression in renal tissue and serum Gal-3 levels were elevated in patients with SLE nephritis versus healthy controls; moreover, they reflected disease activity. These findings suggest that Gal-3 might contribute to the inflammatory process in SLE. Lupus (2009) 18, 22-28.
引用
收藏
页码:22 / 28
页数:7
相关论文
共 37 条
[21]   Galectin-3-positive cell infiltration in human diabetic nephropathy [J].
Kikuchi, Y ;
Kobayashi, S ;
Hemmi, N ;
Ikee, R ;
Hyodo, N ;
Saigusa, T ;
Namikoshi, T ;
Yamada, M ;
Suzuki, S ;
Miura, S .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2004, 19 (03) :602-607
[22]  
Lee YJ, 2007, CLIN EXP RHEUMATOL, V25, pS41
[23]   Identification of autoantibodies associated with systemic lupus erythematosus [J].
Lim, Y ;
Lee, DY ;
Lee, S ;
Park, SY ;
Kim, J ;
Cho, B ;
Lee, H ;
Kim, HY ;
Lee, E ;
Song, YW ;
Jeoung, DI .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 295 (01) :119-124
[24]   Soluble galectin-3 is a strong, colonic epithelial-cell-derived, lamina propria fibroblast-stimulating factor [J].
Lippert, E. ;
Falk, W. ;
Bataille, F. ;
Kaehne, T. ;
Naumann, M. ;
Goeke, M. ;
Herfarth, H. ;
Schoelmerich, J. ;
Rogler, G. .
GUT, 2007, 56 (01) :43-51
[25]   Nucling mediates apoptosis by inhibiting expression of galectin-3 through interference with nuclear factor κB signalling [J].
Liu, L ;
Sakai, T ;
Sano, N ;
Fukui, K .
BIOCHEMICAL JOURNAL, 2004, 380 :31-41
[26]   Determinants in the N-terminal domains of galectin-3 for secretion by a novel pathway circumventing the endoplasmic reticulum-Golgi complex [J].
Menon, RP ;
Hughes, RC .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1999, 264 (02) :569-576
[27]  
Nieminen J, 2005, J LEUKOCYTE BIOL, V78, P1127
[28]   Regulation of cellular adhesion to extracellular matrix proteins by galectin-3 [J].
Ochieng, J ;
Leite-Browning, ML ;
Warfield, P .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 246 (03) :788-791
[29]   Galectin 3 and its binding protein in rheumatoid arthritis [J].
Ohshima, S ;
Kuchen, S ;
Seemayer, CA ;
Kyburz, D ;
Hirt, A ;
Klinzing, S ;
Michel, BA ;
Gay, RE ;
Liu, FT ;
Gay, S ;
Neidhart, M .
ARTHRITIS AND RHEUMATISM, 2003, 48 (10) :2788-2795
[30]   Human galectin-3 is a novel chemoattractant for monocytes and macrophages [J].
Sano, H ;
Hsu, DK ;
Yu, L ;
Apgar, JR ;
Kuwabara, I ;
Yamanaka, T ;
Hirashima, M ;
Liu, FT .
JOURNAL OF IMMUNOLOGY, 2000, 165 (04) :2156-2164