4.5 Article

Neurogranin phosphorylation fine-tunes long-term potentiation

期刊

EUROPEAN JOURNAL OF NEUROSCIENCE
卷 33, 期 2, 页码 244-250

出版社

WILEY
DOI: 10.1111/j.1460-9568.2010.07506.x

关键词

calmodulin; NMDARs; PKC; rat hippocampus; synaptic plasticity

资金

  1. US National Institute on Aging [AG032320]
  2. Alzheimer's Association
  3. American Thyroid Association
  4. NATIONAL INSTITUTE ON AGING [R01AG032320] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Learning-related potentiation of synaptic strength at Cornu ammonis subfield 1 (CA1) hippocampal excitatory synapses is dependent on neuronal activity and the activation of glutamate receptors. However, molecular mechanisms that regulate and fine-tune the expression of long-term potentiation (LTP) are not well understood. Recently it has been indicated that neurogranin (Ng), a neuron-specific, postsynaptic protein that is phosphorylated by protein kinase C, potentiates synaptic transmission in an LTP-like manner. Here, we report that a Ng mutant that is unable to be phosphorylated cannot potentiate synaptic transmission in rat CA1 hippocampal neurons and results in a submaximal expression of LTP. Our results provide the first evidence that the phosphorylation of Ng can regulate LTP expression.

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