Tumor necrosis factor beta and ultraviolet radiation are potent regulators of human keratinocyte ICAM-1 expression
Journal Article
·
· Journal of Investigative Dermatology; (USA)
- Univ. of Freiburg (Germany, F.R.)
Intercellular adhesion molecule-1 (ICAM-1) functions as a ligand of leukocyte function-associated antigen-1 (LFA-1), as well as a receptor for human picorna virus, and its regulation thus affects various immunologic and inflammatory reactions. The weak, constitutive ICAM-1 expression on human keratinocytes (KC) can be up-regulated by cytokines such as interferon-gamma (IFN gamma) and tumor necrosis factor alpha (TNF alpha). In order to further examine the regulation of KC ICAM-1 expression, normal human KC or epidermoid carcinoma cells (KB) were incubated with different cytokines and/or exposed to ultraviolet (UV) radiation. Subsequently, ICAM-1 expression was monitored cytofluorometrically using a monoclonal anti-ICAM-1 antibody. Stimulation of cells with recombinant human (rh) interleukin (IL) 1 alpha, rhIL-4, rhIL-5, rhIL-6, rh granulocyte/macrophage colony-stimulating factor (GM-CSF), rh interferon alpha (rhIFN alpha), and rh transforming growth factor beta (TGF beta) did not increase ICAM-1 surface expression. In contrast, rhTNF beta significantly up-regulated ICAM-1 expression in a time- and dose-dependent manner. Moreover, the combination of rhTNF beta with rhIFN gamma increased the percentage of ICAM-1-positive KC synergistically. This stimulatory effect of rhTNF beta was further confirmed by the demonstration that rhTNF beta was capable of markedly enhancing ICAM-1 mRNA expression in KC. Finally, exposure of KC in vitro to sublethal doses of UV radiation (0-100 J/m2) prior to cytokine (rhIFN tau, rhTNF alpha, rhTNF beta) stimulation inhibited ICAM-1 up-regulation in a dose-dependent fashion. These studies identify TNF beta and UV light as potent regulators of KC ICAM-1 expression, which may influence both attachment and detachment of leukocytes and possibly viruses to KC.
- OSTI ID:
- 6790357
- Journal Information:
- Journal of Investigative Dermatology; (USA), Journal Name: Journal of Investigative Dermatology; (USA) Vol. 95:2; ISSN 0022-202X; ISSN JIDEA
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
560120* -- Radiation Effects on Biochemicals
Cells
& Tissue Culture
63 RADIATION, THERMAL, AND OTHER ENVIRON. POLLUTANT EFFECTS ON LIVING ORGS. AND BIOL. MAT.
ADHESION
ANIMAL CELLS
ANIMALS
ANTIBODIES
BIOLOGICAL EFFECTS
BIOLOGICAL FUNCTIONS
BIOLOGICAL RADIATION EFFECTS
CARCINOMAS
CELL FLOW SYSTEMS
DISEASES
DOSE-RESPONSE RELATIONSHIPS
ELECTROMAGNETIC RADIATION
FUNCTIONS
GROWTH FACTORS
INTERFERON
IRRADIATION
KERATIN
LYMPHOKINES
MAMMALS
MAN
MEMBRANE PROTEINS
MICROORGANISMS
MITOGENS
MONOCLONAL ANTIBODIES
NEOPLASMS
ORGANIC COMPOUNDS
PARASITES
PRIMATES
PROTEINS
RADIATION EFFECTS
RADIATIONS
RECEPTORS
SCLEROPROTEINS
SUBLETHAL IRRADIATION
SYNERGISM
TIME DEPENDENCE
TUMOR CELLS
ULTRAVIOLET RADIATION
VERTEBRATES
VIRUSES
Cells
& Tissue Culture
63 RADIATION, THERMAL, AND OTHER ENVIRON. POLLUTANT EFFECTS ON LIVING ORGS. AND BIOL. MAT.
ADHESION
ANIMAL CELLS
ANIMALS
ANTIBODIES
BIOLOGICAL EFFECTS
BIOLOGICAL FUNCTIONS
BIOLOGICAL RADIATION EFFECTS
CARCINOMAS
CELL FLOW SYSTEMS
DISEASES
DOSE-RESPONSE RELATIONSHIPS
ELECTROMAGNETIC RADIATION
FUNCTIONS
GROWTH FACTORS
INTERFERON
IRRADIATION
KERATIN
LYMPHOKINES
MAMMALS
MAN
MEMBRANE PROTEINS
MICROORGANISMS
MITOGENS
MONOCLONAL ANTIBODIES
NEOPLASMS
ORGANIC COMPOUNDS
PARASITES
PRIMATES
PROTEINS
RADIATION EFFECTS
RADIATIONS
RECEPTORS
SCLEROPROTEINS
SUBLETHAL IRRADIATION
SYNERGISM
TIME DEPENDENCE
TUMOR CELLS
ULTRAVIOLET RADIATION
VERTEBRATES
VIRUSES