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Glutamate receptor trafficking and protein synthesis mediate the facilitation of LTP by secreted amyloid precursor protein-alpha

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Kochen,  Lisa
Synaptic Plasticity Department, Max Planck Institute for Brain Research, Max Planck Society;

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tom Dieck,  Susanne
Synaptic Plasticity Department, Max Planck Institute for Brain Research, Max Planck Society;

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Schuman,  Erin
Synaptic Plasticity Department, Max Planck Institute for Brain Research, Max Planck Society;

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引用

Mockett, B. G., Guèvremont, D., Elder, M. K., Parfitt, K. D., Peppercorn, K., Morrissey, J., Singh, A., Hintz, T. J., Kochen, L., tom Dieck, S., Schuman, E., Tate, W. P., Williams, J. M., & Abraham, W. C. (2019). Glutamate receptor trafficking and protein synthesis mediate the facilitation of LTP by secreted amyloid precursor protein-alpha. The Journal of Neuroscience, 39(17), 3188-3203. doi:10.1523/JNEUROSCI.1826-18.2019.


引用: https://hdl.handle.net/21.11116/0000-0007-A8A2-4
要旨
Secreted amyloid precursor protein-alpha (sAPP) has growth factor-like properties and can modulate long-term potentiation (LTP)and memory. Here, we demonstrate that exposure to sAPPconverts short-lasting LTP into protein-synthesis-dependent late LTP inhippocampalslicesfrommalerats.sAPPhadnodiscernableeffect.WehypothesizedthatsAPPfacilitatedLTPviaregulatedglutamatereceptor trafficking anddenovoprotein synthesis. We found using a linear mixed model that sAPPstimulated trafficking of GluA2-lacking AMPARs, as well as NMDARs to the extrasynaptic cell surface, in a calcium/calmodulin-dependent kinase II and protein kinaseG-dependent manner. Both cell surface receptor accumulation and LTP facilitation were present even after sAPPwashout and inhibi-tion ofreceptor trafficking or protein synthesis prevented all these effects. Direct visualization of newly synthesized proteins (FUNCAT-PLA)confirmed the ability of sAPPto stimulatedenovoprotein synthesis and revealed GluA1 as one of the upregulated proteins. Therefore, sAPPgenerates a coordinated synthesis and trafficking of glutamate receptors to the cell surface that facilitate LTP