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PMID: 16984263 Published · ppublish English Journal Article Research Support, N.I.H., Extramural

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

Experimental dermatology ·Vol. 15 ·No. 10 ·2006-10-00 ·Pages 808-14

HogenEsch H, Dunham A, Seymour R, Renninger M, Sundberg JP

Abstract

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.

MeSH Terms
Animals Chronic Disease Dermatitis/genetics,metabolism,pathology Dermatitis, Contact/etiology,genetics,metabolism Dinitrofluorobenzene/adverse effects Disease Models, Animal Female Gene Expression Regulation, Enzymologic/drug effects Interleukin-4/pharmacology Lectins/genetics,metabolism Macrophages/drug effects,metabolism,pathology Male Mast Cells/drug effects,metabolism,pathology Mice Mice, Inbred C57BL Mice, Mutant Strains RNA, Messenger/genetics,metabolism Skin/metabolism,pathology beta-N-Acetylhexosaminidases/genetics,metabolism
Chemicals
Lectins RNA, Messenger Interleukin-4 Dinitrofluorobenzene Chil3 protein, mouse beta-N-Acetylhexosaminidases
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
HogenEsch Harm
Department of Veterinary Pathobiology, Purdue University, 725 Harrison Street, West Lafayette, IN 47907, USA. [email protected]
Dunham Anisa
Seymour Rosemarie
Renninger Matthew
Sundberg John P
Article Info
Journal
Experimental dermatology
Abbr.
Exp Dermatol
ISSN
0906-6705
Published
2006-10-00
Pages
808-14
Language
English
Region
Denmark
NLM ID
9301549
Subset
IM
Grants
NIAMS NIH HHS · AR 49288 · United States
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