Expression of chitinase-like proteins in the skin of chronic proliferative dermatitis (cpdm/cpdm) mice

被引:26
作者
HogenEsch, Harm
Dunham, Anisa
Seymour, Rosemarie
Renninger, Matthew
Sundberg, John P.
机构
[1] Purdue Univ, Dept Vet Pathobiol, W Lafayette, IN 47907 USA
[2] Jackson Lab, Bar Harbor, ME 04609 USA
关键词
dermatitis; chitinase-like proteins; macrophages; mast cells; mouse;
D O I
10.1111/j.1600-0625.2006.00483.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Mammalian chitinase-like proteins belong to a family of proteins structurally related to chitinases but devoid of enzymatic activity. They have a postulated role in remodeling of extracellular matrix and defense mechanisms against chitin-containing pathogens. The expression of these proteins is increased in parasitic infections and allergic airway disease, but their expression in dermatitis has not been examined. The mRNA expression of two chitinase 3-like (Chi3L) proteins, Chi3L3 (Ym1) and Chi3L4 (Ym2), was determined in the skin of normal mice, chronic proliferative dermatitis (cpdm/cpdm) mutant mice and mice with experimentally induced contact hypersensitivity reaction. The localization of Chi3L3 and Chi3L4 proteins in cells was determined by fluorescence microscopy of double-labeled frozen sections of skin, and confirmed in vitro by stimulation of macrophages and mast cells with cytokines. Quantitative RT-PCR demonstrated a 976-fold increase of Chi3l4 mRNA expression and a 24-fold increase of Chi3l3 mRNA expression in the skin of cpdm/cpdm mice. Their expression was also increased in the ears of mice with 2,4-dinitrofluorobenzene-induced contact hypersensitivity, but the increase was greater for Chi3l3 mRNA (51-fold) than Chi3l4 mRNA (32-fold). Western blot analysis with an antibody against Chi3L3 and Chi3L4 confirmed the increased amount of these proteins in the skin of cpdm/cpdm mice. Two-color immunofluorescence identified macrophages, dendritic cells and mast cells as cellular sources of Chi3L3 and Chi3L4 proteins. Eosinophils and neutrophils did not contain detectable concentrations of these proteins. Treatment of macrophages and mast cells in vitro with interleukin-4 induced expression of Chi3l3 and Chi3l4 mRNA.
引用
收藏
页码:808 / 814
页数:7
相关论文
共 41 条
[21]   IL-4 dependent alternatively-activated macrophages have a distinctive in vivo gene expression phenotype [J].
Loke P. ;
Nair M.G. ;
Parkinson J. ;
Guiliano D. ;
Blaxter M. ;
Allen J.E. .
BMC Immunology, 3 (1)
[22]   MURINE EOSINOPHIL GRANULOCYTES BIND THE MURINE MACROPHAGE-MONOCYTE SPECIFIC MONOCLONAL-ANTIBODY F4/80 [J].
MCGARRY, MP ;
STEWART, CC .
JOURNAL OF LEUKOCYTE BIOLOGY, 1991, 50 (05) :471-478
[23]   Mast cells [J].
Metcalfe, DD ;
Baram, D ;
Mekori, YA .
PHYSIOLOGICAL REVIEWS, 1997, 77 (04) :1033-1079
[24]  
MORRISON BW, 1994, ONCOGENE, V9, P3417
[25]   Chitinase and Fizz family members are a generalized feature of nematode infection with selective Upregulation of Ym1 and F10.1 by antigen-presenting cells [J].
Nair, MG ;
Gallagher, LJ ;
Taylor, MD ;
Loke, P ;
Coulson, PS ;
Wilson, RA ;
Maizels, RM ;
Allen, JE .
INFECTION AND IMMUNITY, 2005, 73 (01) :385-394
[26]   Macrophages in chronic type 2 inflammation have a novel phenotype characterized by the abundant expression of Ym1 and Fizz1 that can be partly replicated in vitro [J].
Nair, MG ;
Cochrane, DW ;
Allen, JE .
IMMUNOLOGY LETTERS, 2003, 85 (02) :173-180
[27]   Cellular expression of murine Ym1 and Ym2, chitinase family proteins, as revealed by in situ hybridization and immunohistochemistry [J].
Nio, J ;
Fujimoto, W ;
Konno, A ;
Kon, Y ;
Owhashi, M ;
Iwanaga, T .
HISTOCHEMISTRY AND CELL BIOLOGY, 2004, 121 (06) :473-482
[28]   Identification of a novel eosinophil chemotactic cytokine (ECF-L) as a chitinase family protein [J].
Owhashi, M ;
Arita, H ;
Hayai, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (02) :1279-1286
[29]   A new mathematical model for relative quantification in real-time RT-PCR [J].
Pfaffl, MW .
NUCLEIC ACIDS RESEARCH, 2001, 29 (09) :E45
[30]  
Raes G, 2002, J LEUKOCYTE BIOL, V71, P597