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ref: -2021 tags: hippocampal behavior scale plasticity Magee Romani Bittner date: 12-20-2021 22:39 gmt revision:0 [head]

Bidirectional synaptic plasticity rapidly modifies hippocampal representations

  • Normal Hebbian plasticity depends on pre and post synaptic activity & their time course.
  • Three-factor plasticity depends on pre, post, and neuromodulatory activity, typically formalized as an eligibility trace (ET) and instructive signal (IS).
  • Here they show that dendritic-plateau dependent hippocampal place field generation, in particular LTD, is not (quite so) dependent on post synaptic activity.
  • Instead, it appears to be a 'register update' operation, where a new pattern is remembered (through LTP) and an old pattern is forgotten (through LTD).
    • That is, the synapses are updating information, not accumulating information.
  • The eq for a single synapse: ΔW/δt=(W maxW)k +q +(ET*IS)Wk q (ET*IS)\Delta W / \delta t = (W_{max} - W) k^+ q^+(ET * IS) - W k^- q^-(ET * IS)
    • Where k are the learning rates, and q are the nonlinear functions regulating potentiation / depression based on eligibility trace and instructive signal.

I'm still not 100% sure that this excludes any influence on presynaptic activity ... they didn't control for that. But certainly LTD in their model does not require postsynaptic activity; indeed, it may only require net-synaptic homeostasis.

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ref: -0 tags: juxtacellular recording gold mushroom cultured hippocampal neurons Spira date: 02-01-2017 02:44 gmt revision:7 [6] [5] [4] [3] [2] [1] [head]

Large-Scale Juxtacellular Recordings from Cultured Hippocampal Neurons by an Array of Gold-Mushroom Shaped Microelectrodes

  • Micrometer sized Au mushroom MEA electrodes.
  • Functionalized by poly-ethylene-imine (PEI, positively charged)/laminin (extracellular matrix protein) undergo a process to form juxtacellular junctions between the neurons and the gMµEs.
  • No figures, but:
    • Whereas substrate integrated planar MEA record FPs dominated by negative-peak or biphasic-signals with amplitudes typically ranging between 40-100 µV and a signal to noise ratio of ≤ 5,
    • The gMµE-MEA recordings were dominated by positive monophasic action potentials.
    • It is important to note that monophasic high peak amplitudes ≥ 100 µV are rarely obtained using planar electrodes arrays, whereas when using the gMµE-MEA, 34.48 % of the gMµEs recorded potentials ≥ 200 µV and 10.64 % recorded potentials in the range of 300-5,085 µV.
  • So, there is a distribution of coupling, approximately 10% "good".

PMID-27256971 Multisite electrophysiological recordings by self-assembled loose-patch-like junctions between cultured hippocampal neurons and mushroom-shaped microelectrodes.

  • Note 300uV - 1mV extracellular 'juxtacellular' action potentials from these mushroom recordings. This is 2 - 5x better than microwire extacellular in-vivo ephys; coupling is imperfect.
    • Sharp glass-insulated W electrodes, ~ 10Mohm, might achieve better SNR if driven carefully.
  • 2um mushroom cap Au electrodes, 1um diameter 1um long shaft
    • No coating, other than the rough one left by electroplating process.
    • Impedance 10 - 25 Mohm.
  • APs decline within a burst of up to 35% -- electrostatic reasons?
  • Most electrodes record more than one neuron, similar to in-vivo ephys, with less LFP coupling.

PMID-23380931 Multi-electrode array technologies for neuroscience and cardiology

  • The key to the multi-electrode-array ‘in-cell recording’ approach developed by us is the outcome of three converging cell biological principals:
    • (a) the activation of endocytotic-like mechanisms in which cultured Aplysia neurons are induced to actively engulf gold mushroom-shaped microelectrodes (gMμE) that protrude from a flat substrate,
    • (b) the generation of high Rseal between the cell’s membrane and the engulfed gMμE, and
    • (c) the increased junctional membrane conductance.
  • Functionalized the Au mushrooms with an RGD-based peptide
    • RGD is an extracellular matrix binding site on fibronectin, which mediates it's interaction with integrin, a cell surface receptor; it is thought that other elements of fibronectin regulate specificity with its receptor. PMID-2418980