20
Views
21
CrossRef citations to date
0
Altmetric
Original Article

Release of cytokines and proteases from human peripheral blood mononuclear and polymorphonuclear cells following phagocytosis and LPS stimulation

, , &
Pages 461-470 | Received 18 Dec 1995, Accepted 03 May 1996, Published online: 08 Jul 2009
 

Abstract

Release and cellular contents of pro- and anti-inflammatory cytokines, neutro-philic elastase and secretory leukocyte proteinase inhibitor (SLPI) were measured with enzyme-linked immunosorbent assay in peripheral blood mono- and polymorphonuclear cells stimulated with preopsonized yeast cells or lipopolysaccha-ride. Tumour necrosis factor alpha (TNFu) was also measured with a bioassay. TNFα production and soluble TNFα receptor I (sTNF RI) were demonstrated in the environment of both cell populations. The bioassay indicated levels of TNFα far below those detected by ELISA. The overall secretion of cytokines and their inhibitors was found to favour an anti-inflammatory balance in the environment of the stimulated cells. The interleukin-1 receptor antagonist (ILl-ra), compared with interleukin-1β (IL-1β), dominated the secretions from both cell types with a 100- to 1000-fold excess respectively. Most of the translated IL-lβ was not secreted but found associated with the cellular compartments. In contrast to lipopolysaccharide (LPS) stimulation, preopsonized yeast cells stimulated a massive release of elastase from neutrophil cells.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.