Am J Physiol Cell Physiol AJP: Endocrinology and Metabolism
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Am J Physiol Cell Physiol (January 14, 2009). doi:10.1152/ajpcell.00478.2008
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Submitted on September 20, 2008
Revised on December 15, 2008
Accepted on January 6, 2009

Effect of pH on L- and D-methionine uptake across the apical membrane of Caco-2 cells

Raquel Martin-Venegas1, M José Rodriguez-Lagunas1, Yves Mercier2, Pierre-André Geraert2, and Ruth Ferrer3*

1 Facultat de Farmacia, Universitat de Barcelona
2 Adisseo France SAS
3 Facultat de Farmcia, Universitat de Barcelona

* To whom correspondence should be addressed. E-mail: rutferrer{at}ub.edu.

The transport systems involved in intestinal methionine (Met) absorption are described as Na+-dependent and Na+-independent mechanisms. However, since recent studies suggest the importance of the H+-gradient as a driving force for intestinal nutrient absorption, the aim of the present work was to test whether Met transport across the apical membrane of Caco-2 cells is affected by extracellular pH. The results show that L- and D-Met uptake was increased by lowering extracellular pH from 7.4 to 5.5, both in the presence and in the absence of Na+. Cis-inhibition experiments revealed that inhibition of L-Met transport by 2-aminobyciclo [2,2,1]heptane-2-carboxylic acid (BCH) or L-lysine (L-Lys) was higher at a pH of 5.5. Moreover, the BCH-insensitive component was not affected by pH, whereas the L-Lys-insensitive component was increased by lowering extracellular pH, thus suggesting the participation of system L. The contribution of another mechanism, sensitive to both BCH and L-Lys, was also considered. The inhibition obtained with taurine (Tau) was also higher at a pH of 5.5, thus suggesting the involvement of system B0,+ on pH-stimulated component. As for D-Met uptake, the results show higher inhibition with L-Lys and Tau at a pH of 5.5 and no effect on the L-Lys- or Tau-insensitive component. In conclusion, Met transport across the apical membrane of Caco-2 cells is increased by low extracellular pH as the result of the stimulation of two transport systems functionally identified with systems L and B0,+ for L-Met and with system B0,+ for D-Met.




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