HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS		QUICK SEARCH:   [advanced] Author: Keyword(s): Year:  Vol:  Page:

This Article Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via Google Scholar Google Scholar Articles by Bristow, A. F. Articles by Poole, S. Search for Related Content PubMed PubMed Citation Articles by Bristow, A. F. Articles by Poole, S.

Activated cells of the monocyte—macrophage lineage produce two forms of the inflammatory cytokine interleukin-1 (IL-1), IL-1 and IL-1β, of which IL-1β is the predominant secreted form and has a wide range of modulatory effects on the endocrine system. Immunoassays of human IL-1β have been described, but are not suitable for measurement of rat and mouse IL-1β because of limited cross-reactivity. Polyclonal sheep anti-rat or sheep anti-mouse IL-1β antisera were used to develop sensitive and specific immunoradiometric assays for rat and mouse IL-1β. Secretion of IL-1β from endotoxin-activated monocytes or macrophages was measured in vitro or in vivo in both species. In vitro, rat monocytes and mouse macrophages produced IL-1β in response to endotoxin, with a relatively small proportion of total IL-1β being secreted. In vivo, endotoxin stimulated an increase in plasma IL-1β in both animals. The development of these assays will facilitate studies of the role of endogenous IL-1β in animal endocrine models.