| Literature DB >> 30884482 |
Deviyani M Rao1, Della T Phan1, Michelle J Choo1, Amie L Owen1, Anne-Laure Perraud1, Fabienne Gally2.
Abstract
To investigate the role of fatty acid-binding protein 5 (FABP5) in infectious diseases, FABP5-deficient mice were challenged with Listeria monocytogenes, a facultative intracellular bacterial pathogen. Interestingly, FABP5-deficient animals were able to clear the infection within 3 days whereas control wild-type (WT) animals showed comparatively higher bacterial burdens in the liver and spleen. Sections of infected tissues showed an increase in inflammatory foci in WT mice compared to FABP5-deficient mice. FABP5-deficient mice had lower circulating inflammatory cytokines and increased inducible nitric oxide synthase production. FABP5-deficient mouse bone marrow-derived macrophages produced higher levels of nitrite anion than their WT counterparts in response to various stimuli. Additionally, in contrast to FABP5-/- mice, transgenic mice overexpressing FABP5 in myeloid cells (LysM-Cre driven) showed decreased survival rates and increased bacterial burden and inflammatory cytokines. Overall, these findings suggest that increased FABP5 levels correlate with a higher L. monocytogenes bacterial burden and elevated subsequent inflammation.Entities:
Keywords: FABP5; Listeria monocytogenes infection; Macrophages
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Year: 2019 PMID: 30884482 PMCID: PMC6758948 DOI: 10.1159/000496405
Source DB: PubMed Journal: J Innate Immun ISSN: 1662-811X Impact factor: 7.349