Protein kinase C (PKC)- induced phosphorylation is necessary for macrophages to respondfully to bacterial lipopolysaccharides (LPS).
The aim of this project is to investigate the mechanism by which LPS influences PKC-dependent signalling pathways such as those leading to the cytoskeletal rearrangements associated with phagocytosis, membrane traffic, cellular adherence and motility. Dr. Aderem's focus is the molecular characterization of the MARCKS protein, and LPS-inducible PKC substrate, which regulates actin structure at the membrane. He will functionally delete the murine MARCKS null mice. In another approach to determining the role(s) of MARCKS in vivo, a macrophage-specific promoter will be used to generate transgenic mice expressing mutant MARCKS proteins in macrophages. He will characterize the LPS- inducible MARCKS promoter by defining regulatory elements in the 5' upstream region. The intron and the 3' untranslated region will also be analyzed for the presence of regulatory elements. The mechanism by which MARCKS targets to specific membranes will be analyzed by biophysical techniques, and by characterizing MARCKS binding proteins. The role of MARCKS in phagocytosis, lysosome recruitment, and transcytosis will be defined using MARCKS mutants and microbes which modify the phagocytic pathway. He will characterize the role of MARCKS in cell motility by examining actin structure and dynamics, calmodulin, and polarized membrane insertion, immotile cells expressing MARCKS mutants. A novel 50 kDa protein which is induced during phagocytosis in macrophages, and which associates with phagosomes, will also be characterized.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
5R37AI025032-13
Application #
2886554
Study Section
Bacteriology and Mycology Subcommittee 2 (BM)
Program Officer
Kraemer, Kristy A
Project Start
1987-07-01
Project End
2000-04-30
Budget Start
1999-05-01
Budget End
2000-04-30
Support Year
13
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Washington
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
135646524
City
Seattle
State
WA
Country
United States
Zip Code
98195
Warren, Sarah E; Duong, Hien; Mao, Dat Phat et al. (2011) Generation of a Listeria vaccine strain by enhanced caspase-1 activation. Eur J Immunol 41:1934-40
Miao, Edward A; Mao, Dat P; Yudkovsky, Natalya et al. (2010) Innate immune detection of the type III secretion apparatus through the NLRC4 inflammasome. Proc Natl Acad Sci U S A 107:3076-80
Warren, Sarah E; Armstrong, Abraham; Hamilton, M Kristina et al. (2010) Cutting edge: Cytosolic bacterial DNA activates the inflammasome via Aim2. J Immunol 185:818-21
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Hertz, Angie L; Bender, Andrew T; Smith, Kimberly C et al. (2009) Elevated cyclic AMP and PDE4 inhibition induce chemokine expression in human monocyte-derived macrophages. Proc Natl Acad Sci U S A 106:21978-83
Zak, Daniel E; Aderem, Alan (2009) A systems view of host defense. Nat Biotechnol 27:999-1001
Di Paolo, Nelson C; Miao, Edward A; Iwakura, Yoichiro et al. (2009) Virus binding to a plasma membrane receptor triggers interleukin-1 alpha-mediated proinflammatory macrophage response in vivo. Immunity 31:110-21
Bochud, P-Y; Sinsimer, D; Aderem, A et al. (2009) Polymorphisms in Toll-like receptor 4 (TLR4) are associated with protection against leprosy. Eur J Clin Microbiol Infect Dis 28:1055-65
Miao, Edward A; Ernst, Robert K; Dors, Monica et al. (2008) Pseudomonas aeruginosa activates caspase 1 through Ipaf. Proc Natl Acad Sci U S A 105:2562-7
Warren, Sarah E; Mao, Dat P; Rodriguez, April E et al. (2008) Multiple Nod-like receptors activate caspase 1 during Listeria monocytogenes infection. J Immunol 180:7558-64

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