Activation of vascular endothelial cells by IL-1α released by epithelial cells infected with respiratory syncytial virus

Cheng Hsien Chang, Yan Huang, Robert Anderson

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

30 Citas (Scopus)

Resumen

Although pulmonary inflammation is a serious, sometimes life-threatening, consequence of respiratory syncytial virus (RSV) infection, the mechanisms involved are not well understood. Since the process of inflammation is initiated by a complex series of events including the activation of specific adhesion molecules on vascular endothelium, we searched for endothelial cell-activating factors released from RSV-infected epithelial cells. We demonstrate here that vascular endothelial cells exposed to culture supernatants from RSV-infected pulmonary epithelial A549 cells are activated to express increased cell surface ICAM-1, and to a lesser extent, VCAM-1 and E-selectin. IL-1α was identified as the predominant endothelial cell-activating factor by pretreating epithelial cell supernatants with anti-IL-1α antibody. The preferential upregulation of endothelial ICAM-1 (relative to VCAM-1 and E-selectin) by RSV-infected epithelial cell supernatants was replicated by recombinant IL-1α thus confirming IL-1α as a major endothelial cell-activating cytokine released by RSV-infected epithelial cells. Il-1α mediated endothelial cell activation is thus a likely contributory event in the initiation of leukocyte inflammation associated with RSV infection. Crown

Idioma originalEnglish
Páginas (desde-hasta)37-41
Número de páginas5
PublicaciónCellular Immunology
Volumen221
N.º1
DOI
EstadoPublished - ene. 2003

Nota bibliográfica

Funding Information:
This work was supported by the Canadian Institutes of Health Research and Partnership funding from the IWK Grace Health Science Center and the Nova Scotia Health Research Foundation. We are grateful to Andrew C. Issekutz for endothelial cell cultures and for helpful discussions. R.A. is an Associate of the Dalhousie Medical Research Foundation.

ASJC Scopus Subject Areas

  • Immunology

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