Intestinal monoacylglycerol (MG) metabolism is well known to involve its anabolic reesterification to triacylglycerol (TG).We recently provided evidence for enterocyte MG hydrolysis and demonstrated expression of the monoacylglycerol lipase (MGL) gene in human intestinal Caco-2 cells and rodent small intestinal mucosa. Despite the large quantities of MG derived from dietary TG, the regulation of MG metabolism in the intestine has not been previously explored. In the present studies, we examined the mRNA expression, protein expression, and activities of the two known MG-metabolizing enzymes, MGL and MGAT2, in C57BL/6 mouse small intestine, as well as liver and adipose tissues, during development and under nutritional modifications. Results demonstrate that MG metabolism undergoes tissue-specific changes during development. Marked induction of small intestinal MGAT2 protein expression and activity were found during suckling. Moreover, while substantial levels of MGL protein and activity were detected in adult intestine, its regulation during ontogeny was complex, suggesting post-transcriptional regulation of expression. In addition, during the suckling period MG hydrolytic activity is likely to derive from carboxyl ester lipase rather than MGL. In contrast to intestinal MGL, liver MGL mRNA, protein and activity all increased 5-10-fold during development, suggesting that transcriptional regulation is the primary mechanism for hepatic MGL expression. Three weeks of high fat feeding (40% kcal) significantly induced MGL expression and activity in small intestine relative to low fat feeding (10% kcal), but little change was observed upon starvation, suggesting a role for MGL in dietary lipid assimilation following a high fat intake.
sn-2-Monoacylglycerol (MG)2 is one of the major digestive products of dietary triacylglycerol (TG). Along with fatty acid, it is formed by the action of pancreatic triacylglycerol lipase (PTL) in the intestinal lumen, because PTL preferentially cleaves the sn-1 and 3 positions of TG (1). Both hydrolysis products are absorbed as monomers across the apical membrane of the intestinal epithelial cell (1, 2). The mechanism of sn-2-MG uptake into the enterocyte has been demonstrated to be a saturable function of the monomer concentration of sn-2-MG at both apical and basal lateral surfaces of the cell, suggesting carrier-mediated uptake (2, 3). At higher concentrations, a diffusional uptake pathway is also apparent (2, 3). After absorption, sn-2-MG is rapidly reincorporated into TG in the endoplasmic reticulum (ER) via the so-called monoacylglycerol acyltransferase (MGAT) pathway, which is catalyzed by two enzymes, MGAT2 and diacylglycerol acyltransferase (DGAT). Two DGAT isoforms (DGAT1 and 2) have been identified, and both are expressed in small intestine (4, 5). In addition to the MG pathway, the intestine can also synthesize TG via the glycerol-3-phosphate (G3P) pathway, which is the dominant TG synthetic pathway in other tissues such as adipose and liver (1). In the intestine, however, more ...