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IL-1β as a determinant in silica-induced cytokine responses in monocyte-endothelial cell co-culturesDivision of Environmental Medicine, Department for Air Pollution and Noise, Norwegian Institute of Public Health, Oslo, Norway; Biomedical Laboratory Science, Faculty of Health Sciences, Oslo University College, Oslo, Norway jan-inge.herseth{at}hf.hio.no
Division of Environmental Medicine, Department for Air Pollution and Noise, Norwegian Institute of Public Health, Oslo, Norway
Division of Environmental Medicine, Department for Air Pollution and Noise, Norwegian Institute of Public Health, Oslo, Norway
Immunology and Transfusion Medicine, Ullevaal University Hospital, Oslo, Norway
Division of Environmental Medicine, Department for Air Pollution and Noise, Norwegian Institute of Public Health, Oslo, Norway
Alveolar macrophages and endothelial cells are both involved in lung inflammation and remodeling of lung alveolar structures. In the present study, monocytes (precursors for macrophages) were exposed to crystalline silica and examined for pro- and anti-inflammatory cytokine responses in non-contact co-cultures with endothelial cells. The time courses for silica-induced release of tumor necrosis factor (TNF)-
Key Words: cytokines endothelial cells monocytes silica
Human & Experimental Toxicology, Vol. 27, No. 5,
387-399 (2008) This article has been cited by other articles:
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, interleukin (IL)-1β, and IL-8 both from co-cultures and monocyte mono-cultures showed an early peak at 5–10 h, almost no response at 20 h, and a strong increase at 43 h. At 43 h, co-cultures also showed strongly increased IL-6 levels. Steady-state levels of mRNA roughly exhibited the same pattern of early up-regulation and reduced levels at 20 h. Compared with monocyte mono-cultures, silica induced a strong release of IL-1β, IL-6, and IL-8, but not of TNF-