Literature DB >> 18687292

Lipid bodies in innate immune response to bacterial and parasite infections.

Heloisa D'Avila1, Clarissa M Maya-Monteiro, Patricia T Bozza.   

Abstract

Lipid bodies (also known as lipid droplets, adiposomes) are dynamic organelles with key roles in regulating storage and turnover of lipids in different cells and organisms. The emerging role of lipid bodies as inflammatory organelles raises lipid body status to critical regulators of different inflammatory and infectious diseases and key markers of cell activation. Notably, lipid body biogenesis is highly regulated and is cell and stimuli specific. Lipid body structural features, including lipid and protein composition may vary according to the cell type, activation state and inflammatory environment and thus may determine different cellular functions for lipid bodies. Here we will review the morphological and structural aspects of lipid bodies, the regulated mechanisms of formation, as well as lipid body functions in cells involved in the innate immune response during bacterial and parasite infections.

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Year:  2008        PMID: 18687292     DOI: 10.1016/j.intimp.2008.01.035

Source DB:  PubMed          Journal:  Int Immunopharmacol        ISSN: 1567-5769            Impact factor:   4.932


  25 in total

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Review 5.  Macrophage form, function, and phenotype in mycobacterial infection: lessons from tuberculosis and other diseases.

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Review 7.  Foamy macrophages and the progression of the human tuberculosis granuloma.

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8.  The conserved metalloprotease invadolysin localizes to the surface of lipid droplets.

Authors:  Neville Cobbe; Kathryn M Marshall; Shubha Gururaja Rao; Ching-Wen Chang; Francesca Di Cara; Edward Duca; Sharron Vass; Adam Kassan; Margarete M S Heck
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Review 9.  Leukocyte lipid bodies - Biogenesis and functions in inflammation.

Authors:  Patricia T Bozza; Kelly G Magalhães; Peter F Weller
Journal:  Biochim Biophys Acta       Date:  2009-01-21

10.  Azithromycin treatment alters gene expression in inflammatory, lipid metabolism, and cell cycle pathways in well-differentiated human airway epithelia.

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