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Neutrophils alveolar, cytokine production

Chemokines have been found to be produced by an array of cells, including monocytes, alveolar macrophages, neutrophils, platelets, eosinophils, mast cells, T and B lymphocytes, NK cells, keratinocytes, mesangial cells, epithelial cells, hepatocytes, flbroblasts, smooth muscle cells, mesothelial cells, and endothelial cells. These cells can produce chemokines in response to a variety of factors, including viruses, bacterial products, IL-1, TNF, C5a, LTB4, and IFNs. The production of chemokines by both immune and nonimmune cells supports the contention that these cytokines may play a pivotal role in orchestrating chronic inflammation. We will focus our discussion on the role of the CXC and CC chemokine families in the context of pulmonary fibrosis. [Pg.241]

Cytokine-induced neutrophil chemoattractant production in lipopolysaccharide-stimulated rat alveolar macrophages is regulated by the polyamine, putrescine (Kamoi et al. 1997). [Pg.372]

Crippen TL, Klasing KC, Hyde DM. Cytokine-induced neutrophil chemoattractant production by primary rat alveolar type It eells. Inflammation 1995 19 575-586. [Pg.391]


See other pages where Neutrophils alveolar, cytokine production is mentioned: [Pg.83]    [Pg.550]    [Pg.555]    [Pg.399]    [Pg.210]    [Pg.310]    [Pg.74]    [Pg.243]    [Pg.651]    [Pg.906]    [Pg.2309]    [Pg.214]    [Pg.566]    [Pg.144]    [Pg.200]    [Pg.238]    [Pg.393]    [Pg.179]    [Pg.222]    [Pg.350]   
See also in sourсe #XX -- [ Pg.550 ]




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