Conjunctive input processing drives feature selectivity in hippocampal CA1 neurons
By Katie C. Bittner, Christine Grienberger, Sachin P. Vaidya, Aaron D. Milstein, J. Macklin, J. Suh, S. Tonegawa, Jeffrey C. Magee. 2015
490 citations recorded by the source corpus.
Feature-selective firing allows networks to produce representations of the external and internal environments. Despite its importance, the mechanisms generating neuronal feature selectivity are incompletely understood. In many cortical microcircuits the integration of two functionally distinct inputs occurs nonlinearly through generation of active dendritic signals that drive burst firing and robust plasticity. To examine the role of this processing in feature selectivity, we recorded CA1 pyramidal neuron membrane potential and local field potential in mice running on a linear treadmill. We found that dendritic plateau potentials were produced by an interaction between properly timed input from entorhinal cortex and hippocampal CA3. These conjunctive signals positively modulated the firing of previously established place fields and rapidly induced new place field formation to produce feature selectivity in CA1 that is a function of both entorhinal cortex and CA3 input. Such selectivity could allow mixed network level representations that support context-dependent spatial maps.
Subfields: Cellular and Molecular Neuroscience, Cognitive Neuroscience
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Cellular and Molecular Neuroscience
- Johanni Brea
- Dane S. Corneil
- Vasiliki Liakoni
- Marco P Lehmann
- Jeffrey C. Magee
- Wulfram Gerstner
- Christine Grienberger
- Friedemann Zenke
In Cognitive Neuroscience
- Johanni Brea
- Wulfram Gerstner
- Dane S. Corneil
- Vasiliki Liakoni
- Marco P Lehmann
- Jeffrey C. Magee
- Christine Grienberger
- Friedemann Zenke
Citations in the corpus
- Synaptic Plasticity Forms and Functions. (2020, background): “…of a silent CA1 cell, and the large, long-lasting depolarization associated with the plateau effectively spreads throughout the neuron (Grienberger et al. 2014), inducing a potentiation of excitatory synaptic inputs that arrive around the plateau (Bittner et al. 2015, 2017) ( Figure 4 b ).”
- Eligibility Traces and Plasticity on Behavioral Time Scales: Experimental Support of NeoHebbian Three-Factor Learning Rules (2018, methodology): “However, only those neurons that also get, at the same time, sufficiently strong input from CA3 might develop the visible plateau potential (Bittner et al., 2015).”