Advanced search
Start date
Betweenand
(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

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

Full text
Author(s):
de Lima-Salgado, Thais Martins [1] ; Alba-Loureiro, Tatiana C. [2] ; do Nascimento, Caroline S. [2] ; Nunes, Maria T. [2] ; Curi, Rui [2]
Total Authors: 5
Affiliation:
[1] Univ Sao Paulo, Sch Med, Dept Emergency Med, Lab Clin Emergency LIM51, BR-01246903 Sao Paulo - Brazil
[2] Univ Sao Paulo, Inst Biomed Sci, Dept Physiol & Biophys, BR-05508900 Sao Paulo - Brazil
Total Affiliations: 2
Document type: Journal article
Source: Cell Biochemistry and Biophysics; v. 59, n. 2, p. 89-97, MAR 2011.
Web of Science Citations: 24
Abstract

Many macrophage functions are modulated by fatty acids (FAs), including cytokine release, such as tumor necrosis factor-alpha (TNF-alpha). TNF-alpha 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 mu M of saturated (palmitic and stearic acids), monounsaturated (oleic acid) and polyunsaturated (linoleic acid) FAs on TNF-alpha 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-alpha secretion by the cells. Saturated FAs were potent inducers of TNF-alpha 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-alpha. (AU)

FAPESP's process: 06/02709-3 - Efeitos de acidos graxos sobre a producao e sinalizacao de tnf alfa em macrofagos.
Grantee:Thais Martins de Lima Salgado
Support Opportunities: Scholarships in Brazil - Post-Doctoral