Abstract

Although system A is present at the blood-brain barrier (BBB), the physiological roles of system A have not been clarified. The efflux transport of the substrates of system A, such as l-proline (l-Pro), glycine (Gly), and α-methylaminoisobutyric acid (MeAIB), across the BBB was investigated using the in vivo Brain Efflux Index method. Over a period of 40 min,l-[³H]Pro and [³H]Gly underwent efflux from the brain, whereas [³H]MeAIB did not. The efflux of l-[³H]Pro was inhibited by the presence of unlabeled l-Pro and MeAIB, suggesting that carrier-mediated efflux transport of l-Pro across the BBB is involved in system A. l-[³H]Pro uptake by TR-BBB cells, used as an in vitro BBB model, was Na⁺-dependent with high-affinity (K _m1 = 425 μM) and low-affinity (K _m2 = 10.8 mM) saturable processes. The manner of inhibition of l-[³H]Pro uptake for amino acids was consistent with system A. Although GlnT, ATA2, and ATA3 mRNA were all expressed in TR-BBB cells, ATA2 mRNA was predominant. Under hypertonic conditions, ATA2 mRNA in TR-BBB cells was induced by up to 373%, and it activated [³H]MeAIB uptake. In light of these observations, our results indicate thatl-Pro and Gly are transported from the brain across the BBB, whereas MeAIB is retained in the brain. System A is involved in efflux transport for l-Pro at the BBB. The predominantly expressed ATA2 mRNA at the BBB may play a role in maintaining the concentration of small neutral amino acids and cerebral osmotic pressure in the brain under pathological conditions.