DENDRITIC INTERACTIONS DURING INDUCTION OF PLASTICITY IN MOUSE HIPPOCAMPAL CA1 NEURONS <EM>EX VIVO</EM>
University of Cambridge
Presentation
Date TBA
Event Information
Poster Board
PS03-08AM-525
Poster
View posterAbstract
Using whole-cell patch-clamp recordings from hippocampal slices, I applied a novel stimulation paradigm (pre1–post–pre2) to probe interactions between converging excitatory inputs with distinct arrival times. Strikingly, an excitatory event preceding a post-before-pre pairing converted t-LTD into t-LTP, revealing sensitivity of STDP polarity to input sequence rather than spike timing alone. To investigate the underlying mechanisms, I examined the role of NMDA receptors (NMDARs) using pharmacological manipulations targeting the glutamate binding site, channel pore, and glycine co-agonist site. These experiments uncovered an unconventional form of t-LTD that depends on the glycine binding site and channel pore, but not the glutamate binding site, of presynaptic NMDARs. This profile is consistent with the involvement of GluN1/3-containing NMDARs, suggesting a glycine-activated, glutamate-independent mechanism for t-LTD during early development.
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