Autocrine production of epithelial cell–derived neutrophil attractant-78 induced by granulocyte colony-stimulating factor in neutrophils

Whereas mobilization to inflammatory sites is an important function of neutrophils, it remains to be determined whether granulocyte colony-stimulating factor (G-CSF) stimulates the mobilization of neutrophils to the inflammatory sites. This study compared the expression of more than 9000 genes in ne...

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Veröffentlicht in:Blood 2002-03, Vol.99 (5), p.1863-1865
Hauptverfasser: Suzuki, Sachiko, Kobayashi, Masanobu, Chiba, Kouji, Horiuchi, Iori, Wang, Jingxin, Kondoh, Takeshi, Hashino, Satoshi, Tanaka, Junji, Hosokawa, Masuo, Asaka, Masahiro
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Sprache:eng
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Zusammenfassung:Whereas mobilization to inflammatory sites is an important function of neutrophils, it remains to be determined whether granulocyte colony-stimulating factor (G-CSF) stimulates the mobilization of neutrophils to the inflammatory sites. This study compared the expression of more than 9000 genes in neutrophils treated with and without G-CSF with the use of a DNA microarray system to determine the effects of G-CSF on the function of neutrophils. It was found that messenger RNA expression of epithelial cell–derived neutrophil attractant-78 (ENA-78), which has been reported to be a chemotactic factor for neutrophils, was induced by G-CSF in neutrophils. The study demonstrated that the supernatant of G-CSF–treated neutrophils induced the chemotaxis of neutrophils and that anti–ENA-78 antibody and anti–CXCR-2 antibody inhibited the chemotaxis. These data suggest that G-CSF may enhance the mobilization of neutrophils and consequently augment the accumulation of neutrophils in the inflammatory sites through the secretion of ENA-78.
ISSN:0006-4971
1528-0020
DOI:10.1182/blood.V99.5.1863.h8001863_1863_1865