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Differential roles of Rap1 and Rap2 small GTPases in neurite retraction and synapse elimination in hippocampal spiny neurons
Author(s) -
Fu Zhanyan,
Lee Sang Hyoung,
Simonetta Alyson,
Hansen Jonathan,
Sheng Morgan,
Pak Daniel T. S.
Publication year - 2007
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.2006.04195.x
Subject(s) - ampa receptor , dendritic spine , dendritic filopodia , excitatory postsynaptic potential , neuroscience , microbiology and biotechnology , neurotransmission , biology , synapse , dendrite (mathematics) , hippocampal formation , excitatory synapse , synaptic plasticity , postsynaptic potential , actin remodeling of neurons , inhibitory postsynaptic potential , chemistry , glutamate receptor , actin cytoskeleton , receptor , biochemistry , cytoskeleton , geometry , mathematics , cell
The Rap family of small GTPases is implicated in the mechanisms of synaptic plasticity, particularly synaptic depression. Here we studied the role of Rap in neuronal morphogenesis and synaptic transmission in cultured neurons. Constitutively active Rap2 expressed in hippocampal pyramidal neurons caused decreased length and complexity of both axonal and dendritic branches. In addition, Rap2 caused loss of dendritic spines and spiny synapses, and an increase in filopodia‐like protrusions and shaft synapses. These Rap2 morphological effects were absent in aspiny interneurons. In contrast, constitutively active Rap1 had no significant effect on axon or dendrite morphology. Dominant‐negative Rap mutants increased dendrite length, indicating that endogenous Rap restrains dendritic outgrowth. The amplitude and frequency of α‐amino‐3‐hydroxy‐5‐methylisoxazole‐4‐propionate (AMPA)‐mediated miniature excitatory postsynaptic currents (mEPSCs) decreased in hippocampal neurons transfected with active Rap1 or Rap2, associated with reduced surface and total levels of AMPA receptor subunit GluR2. Finally, increasing synaptic activity with GABA A receptor antagonists counteracted Rap2’s inhibitory effect on dendrite growth, and masked the effects of Rap1 and Rap2 on AMPA‐mediated mEPSCs. Rap1 and Rap2 thus have overlapping but distinct actions that potentially link the inhibition of synaptic transmission with the retraction of axons and dendrites.