Molecular Mechanisms by Which Saturated Fatty Acids Modulate TNF-α Expression in Mouse Macrophage Lineage

• Published in: Cell biochemistry and biophysics 2011-03, Vol.59 (2), p.89-97
• Main Authors: de Lima-Salgado, Thais Martins, Alba-Loureiro, Tatiana C, do Nascimento, Caroline S, Nunes, Maria T, Curi, Rui
• Format: Article
• Language: English
• Subjects: Animals; Biochemistry; Biological and Medical Physics; Biomedical and Life Sciences; Biophysics; Biotechnology; Cell Biology; Cells, Cultured; Fatty Acids - pharmacology; gene expression; Gene Expression Regulation - drug effects; Inflammation Mediators - pharmacology; Life Sciences; Linoleic Acid - pharmacology; Macrophages - cytology; Macrophages - drug effects; Macrophages - metabolism; messenger RNA; Mice; Oleic Acid - pharmacology; Original Research; Pharmacology/Toxicology; Saturated fatty acid; Stearic Acids - pharmacology; TNF-α; transcription factors; Transcription Factors - drug effects; Tumor Necrosis Factor-alpha - genetics; Tumor Necrosis Factor-alpha - metabolism
• ISSN: 1085-9195; 1559-0283
• DOI: 10.1007/s12013-010-9117-9

Many macrophage functions are modulated by fatty acids (FAs), including cytokine release, such as tumor necrosis factor-α (TNF-α). TNF-α is of great interest due to its role in the inflammation process observed in several diseases such as rheumatoid arthritis, atherosclerosis, and obesity. However, the mechanisms by which FA effects occur have not been completely elucidated yet. In this study, we used a mouse monocyte lineage (J774 cells) to evaluate the effect of 50 and 100 μM of saturated (palmitic and stearic acids), monounsaturated (oleic acid) and polyunsaturated (linoleic acid) FAs on TNF-α production. Alterations in gene expression, poly(A) tail length and activation of transcription factors were evaluated. Oleic and linoleic acids, usually known as neutral or pro-inflammatory FA, inhibited LPS-induced TNF-α secretion by the cells. Saturated FAs were potent inducers of TNF-α expression and secretion under basal and inflammatory conditions (in the presence of LPS). Although the effect of the saturated FA was similar, the mechanism involved in each case seem to be distinct, as palmitic acid increased EGR-1 and CREB binding activity and stearic acid increased mRNA poly(A) tail. These results may contribute to the understanding of the molecular mechanisms by which saturated FAs modulate the inflammatory response and may lead to design of associations of dietary and pharmacological strategies to counteract the pathological effects of TNF-α.