Decreased expression of Intestinal I- and L-FABP levels in rare human genetic lipid malabsorption syndromes.

Abstract

We investigated, for the first time, the expression of I- and L-FABP in two very rare hereditary lipid malabsorption syndromes as compared with normal subjects. Abetalipoproteinemia (ABL) and Anderson's disease (AD) are characterized by an inability to export alimentary lipids as chylomicrons that result in fat loading of enterocytes. Duodeno-jejunal biopsies were obtained from 14 fasted normal subjects, and from four patients with ABL and from six with AD. Intestinal FABP expression was investigated by immuno-histochemistry, western blot, ELISA and Northern blot analysis. In contrast to normal subjects, the cellular immunostaining for both FABPs was clearly decreased in patients, as the enterocytes became fat-laden. In patients with ABL, the intestinal contents of I- (60.7 +/- 13.38 ng/mg protein) and L-FABP (750.3 +/- 121.3 ng/mg protein) are significantly reduced (50 and 35%, P < 0.05, respectively) as compared to normal subjects (I-135.3 +/- 11.1 ng, L-1211 +/- 110 ng/mg protein). In AD, the patients also exhibited decreased expression (50%, P < 0.05; I-59 +/- 11.88 ng, L-618.2 +/- 104.6 ng/mg protein). Decreased FABP expression was not associated with decreased mRNA levels. The results suggest that enterocytes might regulate intracellular FABP content in response to intracellular fatty acids, which we speculate may act as lipid sensors to prevent their intracellular transport.

• Authors: S Guilmeau, I Niot, J P Laigneau, H Devaud, V Petit, N Brousse, R Bouvier, L Ferkdadji, C Besmond, L P Aggerbeck, A Bado, M E Samson-Bouma
• Journal: Histochemistry and cell biology (Histochem Cell Biol) Vol. 128 Issue 2 Pg. 115-23 (Aug 2007) ISSN: 0948-6143 [Print] Germany
• PMID: 17605029 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• FABP1 protein, human
• FABP2 protein, human
• Fatty Acid-Binding Proteins
• RNA, Messenger

Topics

• Abetalipoproteinemia (genetics, metabolism)
• Adolescent
• Adult
• Child
• Fatty Acid-Binding Proteins (genetics, metabolism)
• Female
• Humans
• Immunohistochemistry
• Intestinal Mucosa (metabolism)
• Lipid Metabolism, Inborn Errors (genetics, metabolism)
• Malabsorption Syndromes (genetics, metabolism)
• Male
• RNA, Messenger (metabolism)