Document Detail


The state of differentiation of cultured human keratinocytes determines the level of intercellular adhesion molecule-1 (ICAM-1) expression induced by gamma interferon.
MedLine Citation:
PMID:  1373746     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Inducing the expression of ICAM-1 (CD54) on the surface of epidermal keratinocytes is an important step in initiating leukocyte interaction with the epidermis. We studied the effect of keratinocyte differentiation and of drugs used to treat epidermal inflammation on the induction of this important adhesion molecule. Cell membrane expression of ICAM-1 in cultured human keratinocytes was analyzed using both immunofluorescence and FACS analysis of staining with anti-ICAM-1 monoclonal antibody and was correlated with markers of keratinocyte differentiation. Cell-surface ICAM-1 expression was induced by gamma interferon in all culture conditions, but was significantly greater (p less than 0.014) in cells grown in low-calcium medium ([Ca++] 0.03 mM), and correlated with increased staining for the basal cell keratin K5. The synthetic retinoid Etretin (Ro 10-1670) enhanced the interferon-induced ICAM-1 expression over a wide concentration range (10(-8)-10(-5) M); however, this effect was only seen in the more differentiated cells grown in 0.15 mM and 1.0 mM calcium and not in the cells grown in 0.03 mM calcium. The Etretin effects on intracellular K5 staining paralleled those on cell-surface ICAM-1. Anti-inflammatory glucocorticoids had no effect on ICAM-1 expression in cultured human keratinocytes, even at suboptimal gamma interferon doses (5 U/ml). beta-estradiol, on the other hand, mimicked the Etretin effect, increasing both IFN induction of ICAM-1 expression and K5 staining in more differentiated keratinocytes in 0.15 and 1.0 mM calcium, but not in those in 0.03 mM calcium. Both Etretin and beta-estradiol decreased staining of involucrin, a marker of terminal differentiation, supporting the proposition that in this experimental system these drugs suppress keratinocyte differentiation. The enhanced ICAM-1 induction in keratinocytes with a basal level of differentiation correlates with the in vivo effects of interferon on ICAM-1 and may be a principal determinant in the patterns of ICAM-1 seen in inflammatory skin diseases.
Authors:
M Kashihara-Sawami; D A Norris
Related Documents :
18341576 - Chinese herbal medicine (tuhuai extract) exhibits topical anti-proliferative and anti-i...
19131226 - The involvement of pro-inflammatory cytokines in nephrogenic systemic fibrosis - a mech...
18460896 - Therapeutics and immune-mediated skin disease.
19844666 - Photolytically generated nitric oxide inhibits caspase activity and results in aif-medi...
12417876 - The role of suppressor t cells in regulation of immune responses.
17234346 - Lovastatin protects human neurons against abeta-induced toxicity and causes activation ...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  The Journal of investigative dermatology     Volume:  98     ISSN:  0022-202X     ISO Abbreviation:  J. Invest. Dermatol.     Publication Date:  1992 May 
Date Detail:
Created Date:  1992-05-28     Completed Date:  1992-05-28     Revised Date:  2008-11-21    
Medline Journal Info:
Nlm Unique ID:  0426720     Medline TA:  J Invest Dermatol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  741-7     Citation Subset:  IM    
Affiliation:
Department of Dermatology, University of Colorado School of Medicine, Denver 80262.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Acitretin
Cell Adhesion Molecules / physiology*
Cell Differentiation
Estradiol / pharmacology
Glucocorticoids / pharmacology
Humans
Intercellular Adhesion Molecule-1
Interferon-gamma / pharmacology*
Keratinocytes / chemistry,  cytology*
Male
Protein Precursors / drug effects
Staining and Labeling
Tretinoin / analogs & derivatives,  pharmacology
Grant Support
ID/Acronym/Agency:
AR26427/AR/NIAMS NIH HHS
Chemical
Reg. No./Substance:
0/Cell Adhesion Molecules; 0/Glucocorticoids; 0/Protein Precursors; 126547-89-5/Intercellular Adhesion Molecule-1; 302-79-4/Tretinoin; 50-28-2/Estradiol; 55079-83-9/Acitretin; 60108-77-2/involucrin; 82115-62-6/Interferon-gamma

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Analysis of islet cell antibodies reactivity to a human islet cell line.
Next Document:  Dermal mast cell granules bind interstitial procollagenase and collagenase.