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Liver and intestinal fatty acid binding proteins in control and TGFβ1 gene targeted deficient mice

✍ Scribed by Robert N. Fontaine; Ruanna E. Gossett; Friedhelm Schroeder; Barbara A. O'Toole; Thomas Doetschman; Ann B. Kier


Publisher
Springer
Year
1996
Tongue
English
Weight
454 KB
Volume
159
Category
Article
ISSN
0300-8177

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✦ Synopsis


The effect of transforming growth factor beta-1 (TGF beta 1) expression on fatty acid binding proteins was examined in control and two strains of gene targeted TGF beta 1-deficient mice. Homozygous TGF beta 1-deficient 129 x CF-1, expressing multifocal inflammatory syndrome, had 25% less liver fatty acid binding protein (L-FABP) when compared to control mice. The decrease in L-FABP expression was not due to multifocal inflammatory syndrome since homozygous TGF beta 1-deficient/immunodeficient C3H mice on a SCID background had 36% lower liver L-FABP than controls. This effect was developmentally related and specific to liver, but not the proximal intestine, where L-FABP is also expressed. Finally, the proximal intestine also expresses intestinal-FABP (I-FABP) which decreased 3-fold in the TGF beta 1-deficient/immunodeficient C3H mice only. Thus, TGF beta 1 appears to regulate the expression of L-FABP and I-FABP in the liver and the proximal intestine, respectively.


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## Abstract Intestinal and liver fatty acid binding proteins (I‐ and L‐FABP) are thought to play a role in enterocyte fatty acid (FA) trafficking. Their modulation by cell differentiation and various potential effectors was investigated in the human Caco‐2 cell line. With the acquisition of enteroc