Increases in Calmodulin Abundance and Stabilization of Activated iNOS Mediate Bacterial Killing in RAW 264.7 Macrophages

Journal Article · Tue Aug 01 04:00:00 EDT 2006 · Biochemistry, 45(32):9717-9726

DOI:https://doi.org/10.1021/bi060485p· OSTI ID:891139

Smallwood, Heather S; Shi, Liang; Squier, Thomas C

The rapid activation of macrophages in response to bacterial antigens is central to the innate immune system that permits the recognition and killing of pathogens to limit infection. To understand regulatory mechanisms underlying macrophage activation, we have investigated changes in the abundance of calmodulin (CaM) and iNOS in response to the bacterial cell wall component lipopolysaccharide (LPS) using RAW 264.7 macrophages. Critical to these measurements was the ability to differentiate free iNOS from the CaM-bound (active) form of iNOS associated with nitric oxide generation. We observe a rapid two-fold increase in CaM abundance during the first 30 minutes that is blocked by inhibition of NF?B nuclear translocation or protein synthesis. A similar two-fold increase in the abundance of the complex between CaM and iNOS is observed with the same time dependence. In contrast, there are no detectable increases in the CaM-free (i.e., inactive) form of iNOS within the first hour; it remains at a very low abundance during the initial phase of macrophage activation. Increasing cellular CaM levels in stably transfected cells results in a corresponding increase in the abundance of the CaM/iNOS complex that promotes effective bacterial killing following challenge by Salmonella typhimurium. Thus, LPS-dependent increases in CaM abundance function in the stabilization and activation of iNOS on the rapid time-scale associated with macrophage activation and bacterial killing. These results explain how CaM and iNOS coordinately function to form a stable complex that is part of a rapid host-response that functions within the first 30 minutes following bacterial infection to up-regulate the innate immune system involving macrophage activation.

• Research Organization: Pacific Northwest National Laboratory (PNNL), Richland, WA (US)
• Sponsoring Organization: USDOE
• DOE Contract Number: AC05-76RL01830
• OSTI ID: 891139
• Report Number(s): PNWD-SA-7421
• Journal Information: Biochemistry, 45(32):9717-9726, Journal Name: Biochemistry, 45(32):9717-9726
• Country of Publication: United States
• Language: English

Related Subjects

59 BASIC BIOLOGICAL SCIENCES
60 APPLIED LIFE SCIENCES
ABUNDANCE
ANTIGENS
CALMODULIN
CELL WALL
LIPOPOLYSACCHARIDES
MACROPHAGES
NITRIC OXIDE
PATHOGENS
PROTEINS
SALMONELLA TYPHIMURIUM
STABILIZATION
SYNTHESIS
TIME DEPENDENCE
TRANSLOCATION
macrophage
pathogen
sensors
signal transduction