| Primary Identifier | IPR002984 | Type | Family |
| Short Name | Na/ntran_symport_creatine |
| description | Neurotransmitter transport systems are integral to the release, re-uptake and recycling of neurotransmitters at synapses. High affinity transport proteins found in the plasma membrane of presynaptic nerve terminals and glial cells are responsible for the removal from the extracellular space of released-transmitters, thereby terminating their actions []. Plasma membrane neurotransmitter transporters fall into two structurally and mechanistically distinct families. The majority of the transporters constitute an extensive family of homologous proteins that derive energy from the co-transport of Na+and Cl-, in order to transport neurotransmitter molecules into the cell against their concentration gradient. The family has a common structure of 12 presumed transmembrane helices and includes carriers for gamma-aminobutyric acid (GABA), noradrenaline/adrenaline, dopamine, serotonin, proline, glycine, choline, betaine and taurine. They are structurally distinct from the second more-restricted family of plasma membrane transporters, which are responsible for excitatory amino acid transport. The latter couple glutamate and aspartate uptake to the cotransport of Na+and the counter-transport of K+, with no apparent dependence on Cl-[]. In addition, both of these transporter families are distinct from the vesicular neurotransmitter transporters [, ].A Na+and Cl--coupled creatine transporter has been cloned from human androdent tissues. Initially it was mistaken for a choline transporter [, ].The creatine transporter species homologues are near identical (98% identityhuman vs. rat and rabbit) and they are most closely related to thetransporters reported for taurine, GABA and betaine. Northern blot analysis ofcreatine transporter distribution reveals that the highest levels of mRNAexpression are in: skeletal muscle, kidney and heart, with lower levels inbrain and other tissues. Within the brain, the highest levels were detectedin the cerebellum and hippocampus. This expression pattern correlates wellwith those tissues known to possess a high creatine uptake capacity []. |
