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
[1]   A simple method for the in situ detection of eosinophils [J].
Ain, R ;
Tash, JS ;
Soares, MJ .
JOURNAL OF IMMUNOLOGICAL METHODS, 2002, 260 (1-2) :273-278
[2]   CONJUGATED AVIDIN IDENTIFIES CUTANEOUS RODENT AND HUMAN MAST-CELLS [J].
BERGSTRESSER, PR ;
TIGELAAR, RE ;
THARP, MD .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1984, 83 (03) :214-218
[3]  
Bleau G, 1999, EXS, V87, P211
[4]   Identification of a novel acidic mammalian chitinase distinct from chitotriosidase [J].
Boot, RG ;
Blommaart, EFC ;
Swart, E ;
Ghauharali-van der Vlugt, K ;
Bijl, N ;
Moe, C ;
Place, A ;
Aerts, JMFG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (09) :6770-6778
[5]   A macrophage protein, Ym1, transiently expressed during inflammation is a novel mammalian lectin [J].
Chang, NCA ;
Hung, SI ;
Hwa, KY ;
Kato, I ;
Chen, JE ;
Liu, CH ;
Chang, AC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (20) :17497-17506
[6]   A Brugia malayi homolog of macrophage migration inhibitory factor reveals an important link between macrophages and eosinophil recruitment during nematode infection [J].
Falcone, FH ;
Loke, P ;
Zang, XX ;
MacDonald, AS ;
Maizels, RM ;
Allen, JE .
JOURNAL OF IMMUNOLOGY, 2001, 167 (09) :5348-5354
[7]  
Gijbels MJJ, 1996, AM J PATHOL, V148, P941
[8]   Alternative activation of macrophages [J].
Gordon, S .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (01) :23-35
[9]   Biochemical characterization of endogenously formed eosinophilic crystals in the lungs of mice [J].
Guo, L ;
Johnson, RS ;
Schuh, JCL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (11) :8032-8037
[10]   Ym1 is a neutrophil granule protein that crystallizes in p47phox-deficient mice [J].
Harbord, M ;
Novelli, M ;
Canas, B ;
Power, D ;
Davis, C ;
Godovac-Zimmermann, J ;
Roes, J ;
Segal, AW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (07) :5468-5475