Title of article :
Exclusive expression of transmembrane TNF-α in mice reduces the inflammatory response in early lipid lesions of aortic sinus
Author/Authors :
Matthias Canault، نويسنده , , Franck Peiretti، نويسنده , , Christoph Mueller، نويسنده , , Francis Kopp، نويسنده , , Pierre Morange، نويسنده , , Sylvia Rihs، نويسنده , , Henri Portugal، نويسنده , , Irene Juhan Vague، نويسنده , , Gilles Nalbone، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2004
Pages :
8
From page :
211
To page :
218
Abstract :
We investigated the effect of transmembrane form of tumor necrosis factor-alpha (TNF) on atherosclerosis in mice. We compared the development of early atherosclerotic lesions in the aortic sinus of (1) TNF-deficient mice that express only a non-cleavable transmembrane form of TNF (tmTNF), (2) wild-type (WT) C57BL/6 mice, and (3) TNF-deficient mice (TNF−/−). All mice were fed an atherogenic diet for 20 weeks. Lipid deposition was the most prominent in WT mice (25030±5693 μm2), tended to be lower in tmTNF mice (13640±2190 μm2, P>0.05 versus WT mice) and rare in TNF−/− mice (1408±513 μm2, P<0.05 versus tmTNF and P<0.01 versus WT). Macrophage accumulation was five-fold lower (P<0.01) in tmTNF than in WT mice. In addition, the α-actin immuno-reactivity of medial smooth muscle cells remained intact in tmTNF mice but not in WT mice. In WT mice, the plasma lipid profile was significantly more atherogenic than that of TNF−/− mice (P<0.05), but not significantly different from that of tmTNF mice (P>0.05). These results indicated that in contrast to TNF−/− mice, mice expressing exclusively tmTNF were not completely protected from early atherosclerotic lesion formation, although their lesions have a less inflammatory state than those of WT mice, which underlines the stronger proinflammatory potential of soluble TNF.
Keywords :
dyslipidemia , TNF-? , inflammation , transgenic mice , atherosclerosis
Journal title :
Atherosclerosis
Serial Year :
2004
Journal title :
Atherosclerosis
Record number :
631234
Link To Document :
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