Integrative properties of radial oblique dendrites in hippocampal CA1 pyramidal neurons.

By Attila Losonczy, Jeffrey C. Magee. Neuron, 2006

645 citations recorded by the source corpus.

Subfields: Cellular and Molecular Neuroscience, Neurology

View Paper: https://www.semanticscholar.org/paper/f7add4abe684b4dccc4c6c866df66d9ceed5a53a

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Citations in the corpus

Active properties of neocortical pyramidal neuron dendrites. (2013, background): “The formalization of the cell in three compartments ignores the possibility of local computations performed in thin basal, oblique, and tuft dendrites, for instance with local NMDA and sodium spikes (Larkum et al. 2009, Losonczy & Magee 2006, Mel 1993, Polsky et al. 2004, Schiller et al. 2000).”
Dendritic excitability and synaptic plasticity. (2008, neutral): “A: local spikes in radial oblique dendrites of CA1 pyramidal neurons evoked by multi-site two-photon uncaging of glutamate (450).”
The dendritic branch is the preferred integrative unit for protein synthesis-dependent LTP (2011, methodology): “We then attempted to induce L-LTP by pseudosynchronous (<6 ms) stimulation of multiple spines within a single oblique tertiary apical dendritic branch (Losonczy and Magee, 2006; Losonczy et al., 2008) in ACSF containing 1 mM Mg, 2 mM Ca, and 100 mMof the D1R agonist SKF38393 (GLU+SKF stimulation).”
The Theta-Gamma Neural Code (2013, neutral): “Experimentally, this window is shorter than a gamma cycle (Losonczy and Magee, 2006; Pouille and Neuron.”
Neural syntax: cell assemblies, synapsembles and readers (2010, neutral): “the same dendritic branch and fire synchronously in < 6 ms, as few as 20 neurons may be sufficient to initiate a forward-propagating dendritic spike (Losonczy and Magee, 2006).”
Pyramidal neurons: dendritic structure and synaptic integration (2008, background): “For example, inputs to the main apical dendrite and the oblique apical dendrites might be integrated differentl”
Dendritic spines and distributed circuits. (2011, neutral): “With two-photon uncaging, linear summation is observed when up to 30 neighboring spines are stimulated, although, if more inputs are stimulated, local spikes are triggered (Losonczy and Magee, 2006).”
Channelrhodopsin-2 and optical control of excitable cells (2006, methodology): “19).”
Locally dynamic synaptic learning rules in pyramidal neuron dendrites (2007, neutral): “4e), indicating that uEPSPs or action potentials alone were not sufficient to trigger LTP. STDP therefore was induced at single spines in an input-specific manner.”
COORDINATION OF SIZE AND NUMBER OF EXCITATORY AND INHIBITORY SYNAPSES RESULTS IN A BALANCED STRUCTURAL PLASTICITY ALONG MATURE HIPPOCAMPAL CA1 DENDRITES DURING LTP (2011, background): “Physiological recordings and functional imaging supports this hypothesis (Gray et al., 2006; Losonczy and Magee, 2006; Tsuriel et al., 2006; Harvey and Svoboda, 2007; De Roo et al., 2008; Harvey et al., 2008; Losonczy et al., 2008; Rose et al., 2009; Zhong et al., 2009).”
Anatomical and physiological plasticity of dendritic spines. (2007, background): “Last, 2-photon glutamate uncaging (Matsuzaki et al. 2001, Carter & Sabatini 2004, Sobczyk et al. 2005, Losonczy & Magee 2006) allows the experimenter to select nearly any visualized spine and deliver an arbitrary pattern of glutamate stimulation to the postsynaptic terminal of the selected spine.”