Transforming growth factor-β1 stimulates vascular smooth muscle cell L-proline transport by inducing system A amino acid transporter 2 (SAT2) gene expression

Transforming growth factor-beta1 (TGF-beta1) is a multifunctional cytokine that contributes to arterial remodelling by stimulating vascular smooth muscle cell (SMC) growth and collagen synthesis at sites of vascular injury. Since L-proline is essential for the synthesis of collagen, we examined whether TGF-beta1 regulates the transcellular transport Of L-proline by vascular SMCs. L-Proline uptake by vascular SMCs was primarily sodium-dependent, pH-sensitive, blocked by neutral amino acids and alpha-(methylamino)isobutyric acid, and exhibited trans-inhibition. Treatment of SMCs with TGF-beta1 stimulated L-proline transport in a concentration- and time-dependent manner. The TGF-beta1-mediated L-proline uptake was inhibited by cycloheximide or actinomycin D. Kinetic studies indicated that TGF-beta1-induced L-proline transport was mediated by an increase in transport capacity independent of any changes in the affinity for L-proline. TGF-beta1 stimulated the expression of system A amino acid transporter 2 (SAT2) mRNA in a time-dependent fashion that paralleled the increase in L-proline transport. Reverse transcriptase PCR failed to detect the presence of SAT] or amino acid transporter 3 (ATA3) in either untreated or TGF-beta1-treated SMCs. These results demonstrate that L-proline transport by vascular SMCs is mediated predominantly by the SAT and that TGF-beta1 stimulates SMC L-proline uptake by inducing the expression of the SAT2 gene. The ability of TGF-beta1 to induce SAT2 expression may function to provide SMCs with the necessary levels Of L-proline required for collagen synthesis and cell growth.