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Published on: May 31, 2018
Kinetics of the biosynthesis of complement subcomponent C1q by murine macrophages: effects of stimulation by
A Q Zhou1, M J Herriott, R W Leu
1Biomedical Division-Immunology Section, Samuel Roberts Noble Foundation, Inc., Ardmore, OK 73402.
Insights
Interferon-gamma (IFN-gamma) boosts the production and secretion of complement subcomponent C1q by macrophages. This process enhances the rapid availability of C1q for immune responses.
Area of Science:
- Immunology
- Molecular Biology
- Cell Biology
Background:
- The complement system is crucial for innate and adaptive immunity.
- Macrophages play a key role in immune responses and pathogen clearance.
- Interferon-gamma (IFN-gamma) is a critical cytokine modulating immune cell functions.
Purpose of the Study:
- To investigate the effect of IFN-gamma on complement subcomponent C1q biosynthesis in macrophages.
- To determine the kinetics and regulation of C1q production stimulated by IFN-gamma.
Main Methods:
- Northern blot analysis for C1q mRNA accumulation.
- Complement hemolytic assay for functional C1q in culture supernatants.
- Autoradiography and Western blot analysis for C1q synthesis and intracellular levels.
Main Results:
- IFN-gamma dose-dependently increased C1q mRNA accumulation and extracellular C1q secretion.
- C1q mRNA levels rose within 3 hours and persisted for 24 hours.
- Functional C1q was secreted early (3-9 hours) and sustained for 48 hours, with no significant intracellular accumulation.
Conclusions:
- IFN-gamma promotes rapid and sustained C1q mRNA accumulation and secretion by macrophages.
- The rapid secretion prevents intracellular C1q buildup, suggesting efficient export.
- Primed macrophages provide an abundant source of C1q for immune interactions.
Abstract:
The effects of interferon-gamma (IFN-gamma) on the kinetics of biosynthesis of complement subcomponent C1q by mouse inflammatory peritoneal macrophages were determined. Stimulation of macrophages with various concentrations of IFN-gamma produced a dose-dependent increase in C1q mRNA accumulation which was detected as early as 3 h and sustained through 24 h, as determined by Northern blot analysis. A corresponding early increase in the extracellular accumulation of functional C1q was detected in culture supernatants after 3-9 h stimulation of macrophages with IFN-gamma that was sustained for 24-48 h as determined by a complement hemolytic assay. Autoradiographic analysis of [35S]methionine-labeled secretory C1q confirmed the protracted dose-dependent secretion of C1q by IFN-gamma stimulated macrophages during 24-48 h of culture. Western blot analysis of macrophage lysates indicated no significant changes in endogenous C1q levels following stimulation with IFN-gamma either after 3-9 h or 24-48 h when both C1q mRNA and extracellular accumulation were at their peak. Our results indicate that IFN-gamma promotes early and protracted mRNA accumulation and secretion of C1q by macrophages without intracellular accumulation, presumably due to the rapid rate of secretion of newly synthesized C1q. It is apparent that priming of macrophages with IFN-gamma provides a rapid and abundant source of secretory C1q for potential interaction with various macrophage triggering agents which also bind C1q.
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