期刊
PRION
卷 7, 期 3, 页码 203-208出版社
LANDES BIOSCIENCE
DOI: 10.4161/pri.24503
关键词
prion; zinc; AMPA receptor; ZIP transporter
资金
- Alzheimers Research UK [ART-PG2010-2] Funding Source: researchfish
- Medical Research Council [G0802189] Funding Source: researchfish
- MRC [G0802189] Funding Source: UKRI
- Medical Research Council [G0802189] Funding Source: Medline
Zinc, the most abundant trace metal in the brain, has numerous functions in health and disease. It is released into the synaptic cleft alongside glutamate and this connection between zinc and glutamatergic neurotransmission allows the ion to modulate overall excitability of the brain and influence synaptic plasticity. To maintain healthy synapses, extracellular zinc levels need to be tightly regulated. We recently reported that the cellular prion protein (PrPC) can directly influence neuronal zinc concentrations by promoting zinc uptake via AMPA receptors. The octapeptide repeat region of PrPC is involved in zinc sensing or scavenging and the AMPA receptor provides the channel for transport of the metal across the membrane, facilitated by a direct interaction between the N-terminal polybasic region of PrPC and AMPA receptors. PrPC has been evolutionarily linked to the Zrt/Irt-like protein (ZIP) metal ion transport family with the C-terminus of PrPC sharing sequence similarities with the N-terminal extracellular domains of ZIP 5, 6 and 10. By incorporating the properties of ZIP transporters (both zinc sensing and zinc transport) into two existing neuronal proteins, (PrPC as zinc sensor, AMPA receptor as zinc transporter), neuronal cells are enhancing their biological efficiency and functionality.
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