4.7 Article

The amino acid transporter SNAT2 mediates L-proline-induced differentiation of ES cells

Journal

AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
Volume 300, Issue 6, Pages C1270-C1279

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpcell.00235.2010

Keywords

amino acids; amino acid transporters; embryonic stem cells; differentiation; primitive ectoderm

Funding

  1. University of Melbourne
  2. Australian Stem Cell Centre

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Tan BS, Lonic A, Morris MB, Rathjen PD, Rathjen J. The amino acid transporter SNAT2 mediates L-proline-induced differentiation of ES cells. Am J Physiol Cell Physiol 300: C1270-C1279, 2011. First published February 23, 2011; doi: 10.1152/ajpcell.00235.2010.-There is an increasing appreciation that amino acids can act as signaling molecules in the regulation of cellular processes through modulation of intracellular cell signaling pathways. In culture, embryonic stem (ES) cells can be differentiated to a second, pluripotent cell population, early primitive ectoderm-like cells in response to biological activities within the conditioned medium MEDII. The amino acid L-proline has been identified as a component of MEDII required for ES cell differentiation. Here, we define the primary L-proline transporter on ES and early primitive ectoderm-like cells as sodium-coupled neutral amino acid transporter 2 (SNAT2). SNAT2 uptake of L-proline can be inhibited by the addition of millimolar concentrations of other substrates. The addition of excess amino acids was used to regulate the uptake of L-proline by ES cells, and the effect on differentiation was analyzed. The ability of SNAT2 substrates, but not other amino acids, to prevent changes in morphology, gene expression, and differentiation kinetics suggested that L-proline uptake through SNAT2 was required for ES cell differentiation. These data reveal an unexpected role for amino acid uptake and the amino acid transporter SNAT2 in regulation of pluripotent cells in culture and provides a number of specific, inexpensive, and nontoxic culture additives with the potential to improve the quality of ES cell culture.

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