|BAUCHART-THEVRET, CAROLINE - Children'S Nutrition Research Center (CNRC)|
|CUI, LIWEI - Children'S Nutrition Research Center (CNRC)|
|STOLL, BARBARA - Children'S Nutrition Research Center (CNRC)|
|Burrin, Douglas - Doug|
Submitted to: Journal of Federation of American Societies for Experimental Biology
Publication Type: Abstract Only
Publication Acceptance Date: 4/1/2009
Publication Date: 5/1/2009
Citation: Bauchart-Thevret, C., Cui, L., Stoll, B., Burrin, D. 2009. Arginine-mediated stimulation of intestinal epithelial cell protein synthesis is mTOR-dependent but NO-independent [abstract]. Journal of Federation of American Societies for Experimental Biology. 23:227.7.
Technical Abstract: Arginine (ARG) is an indispensable amino acid in neonates and required for growth. Evidence indicates that intestinal epithelial cells (IEC) are capable of ARG transport, catabolism and synthesis, and express nitric oxide synthase (NOS) to produce NO from ARG. Our aim was to determine whether ARG directly stimulates IEC proliferation, survival, and protein synthesis, and whether this effect is NO-dependent and mediated via mammalian target of rapamycin (mTOR). Neonatal porcine IEC (IPEC-J2) were cultured in a serum-free Dulbecco's Modified Eagles Medium (DMEM) without ARG. After 4-d incubation, we found an increase in cell number (+175%), cell protein (+75%), and DNA content (+50%) with a maximal response at a physiological dose of ARG (0.1 mM). The expression of inducible NOS in IPEC-J2 cells was confirmed by western blot. The ARG-induced protein synthesis response was not inhibited by NO inhibitors (L-NAME or aminoguanidine). Protein synthesis was not increased by addition of a NO donor (SNAP) or the ARG precursor, proline in absence of ARG. However, ARG-induced protein synthesis was markedly decrease (-40%) by rapamycin, an inhibitor of mTOR. We also found ARG (0.5 mM) increased phospho and total mTOR and p70S6 kinase level in IPEC-J2 cells. We conclude that ARG-mediated stimulation of IEC protein synthesis is m-TOR-dependent but NO-independent.