Details

Autor(en) / Beteiligte

• Gutierrez, Maximiliano Gabriel
• Gonzalez, Alexis Perez
• Anes, Elsa
• Griffiths, Gareth

Titel

Role of lipids in killing mycobacteria by macrophages: evidence for NF-[kappa]B-dependent and -independent killing induced by different lipids

Ist Teil von

• Cellular microbiology, 2009-03, Vol.11 (3), p.406-420

Ort / Verlag

Oxford: Hindawi Limited

Erscheinungsjahr

2009

Quelle

Wiley Blackwell Single Titles

Beschreibungen/Notizen

• We have shown that several lipids can modulate the macrophage innate immune response against mycobacteria and enhance their killing. Since NF-κB is required for mycobacterial killing, we tested the ability of lipids to activate NF-κB in uninfected macrophages and those infected with mycobacteria. In uninfected cells, sphingomyelin (SM), phosphatidylinositol-4-phosphate (PIP) and arachidonic acid (AA) enhanced NF-κB activation and the cell surface expression of CD69, a macrophage activation marker regulated by NF-κB. Sphingosine (Sph), sphingosine-1-phosphate (S1P), diacylglycerol (DAG), eicosapentanoic acid (EPA) and phosphatidyl choline (PC) failed to activate either NF-κB or CD69. Ceramide (Cer) activated CD69 expression without activating NF-κB. In Mycobacterium smegmatis- infected cells, NF-κB was transiently activated in a manner that was enhanced by SM, PIP and AA. In contrast Mycobacterium avium mostly repressed NF-κB activation and only SM and AA could induce its partial activation. While lipids that activate NF-κB in uninfected cells tend to kill mycobacteria in macrophages Sph and S1P failed to activate NF-κB under most conditions but nevertheless enhanced killing of M. smegmatis , M. avium and M. tuberculosis H37Rv. Our results argue that both NF-κB-dependent and -independent mechanisms are involved in macrophage killing of mycobacteria and that both mechanisms can be enhanced by selected lipids.