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“Can we predict synchrony and asynchrony in networks coupled by multiple dendritic gap junctions?” Frances K. Skinner Toronto Western Research Institute University Health Network and University of Toronto New York University April 13, 2008 From Scholarpedia: Mathematical Biology article of Frank Hoppensteadt • “highly interdisciplinary nature” • “barriers to collaborations between mathematicians and biologists” • “a shift from mathematical analysis to computer simulation due mostly to improvements in computer power and accessibility.. With the shift being made possible to include more information in models and still derive useful insights from them.” Especially in neuroscience with all the details being uncovered, increasingly sophisticated techniques etc. these comments are very timely. With increasing specialization and interdisciplinarity and potential moving apart of mathematical and biological sciences (or separation of viewpoints) we organized a Theoretical Neuroscience Minisymposium at 2006 Society for Neuroscience meeting, one of the aims being to help counteract this. Interneuron Heterogeneity Domain-specific innervation of hippocampal interneurons apical basal purple –laminae where axonal arbor typically extends turquoise indicates that other interneurons rather than principal cells are targets Different types of interneurons containing calcium-binding proteins and neuropeptides McBain and Fisahn NRN 2001 • General challenge – how to best consider various neurobiological details. • Specific challenge – understanding the contribution of electrical coupling in different contexts. • Outline of Talk: background, discussion of some of our previous work, and then get to question posed for this talk. “Can we predict synchrony and asynchrony in networks coupled by multiple dendritic gap junctions?” Frances K. Skinner Toronto Western Research Institute University Health Network and University of Toronto New York University April 13, 2008 Acknowledgements Tariq Zahid Fernanda Saraga, Leo Ng NSERC of Canada Computing support – RIS of UHN The hippocampus (part of medial temporal lobe) is an intensely studied region of the brain because: • It is associated with memory and learning (i.e., LTP, LTD), epileptic seizures, and neurogenesis. • It exhibits a wide range of population rhythmic activity patterns (<1 to >200 Hz) that are associated with various behavioural states. • It is amenable to experiment, retaining its synaptic circuitry and thus population activities in the slice. EEG activities of mouse hippocampus Electrode location Theta-Gamma SPW-ripples Sharp wave-ripples Spontaneous Rhythmic Field Potentials (SRFPs) (Liang Zhang’s lab; Wu et al. J Physiol 2002, J Neurophysiol 2005) Gillis et al., J. Neurosci. Meth. (2005) Blockade of field rhythms and pyramidal IPSPs by GABA-A receptor antagonist rhythmic activities also dependent on electrical coupling (gap junctions) Background Electrical coupling (i.e., gap junctions) is present in much of the mammalian brain (e.g., inferior olive, striatum, neocortex, hippocampus, retina, thalamus). In particular, gap junctions occur between inhibitory cells, often of the same type, and can be located at sites quite distant (> 200 μm) from the soma. Interneurons represent 10-20% of the neuronal population but may provide the precise temporal structure necessary for ensembles of neurons to perform specific functions. - Buzsáki and Chrobak, 1995 Interneuron Heterogeneity Domain-specific innervation of hippocampal interneurons apical basal purple –laminae where axonal arbor typically extends turquoise indicates that other interneurons rather than principal cells are targets Different types of interneurons containing calcium-binding proteins and neuropeptides McBain and Fisahn NRN 2001 Background Gap junctions located far from cell bodies, at non-proximal sites (basket cells in hippocampus) Gap junctions can be modulated Inhibitory cells have active dendrites, spikes can be generated in dendrites From Fukuda & Kosaka, J Neurosci 2000 Dendrodendritic Gap Junctions Fukuda & Kosaka, J Neurosci 2000 Model (Hippocampal Basket Cell) Passive dendrites 50 mV 372-compartment model developed in NEURON 100 ms Morphology from Gulyas et al.(1999) Saraga et al., J Neurophysiol 2006 WB used for kinetic model basis, Martina and Jonas (1997), Martina et al (1998) used as conductance value basis and spike characteristics and electrophysiological responses from Morin et al. (1996) and van Hooft et al. (2000). “Reduced” 3-compartment model based on matching electrotonic length from soma (Vout) s d d Electrotonic distance to soma (L) Vin 1.2 0.4 0 100 300 500 Anatomical distance to soma (mm) Electrotonic distance from soma (L) Vout=0.14 Vin =0.25 Vout 0.12 0.04 0 100 300 500 Anatomical distance from soma (mm) (Distal) phase response curves (PRCs) Voltage along dendrite s d s d d d Using the reduced model geometry 0.5% Phase Shift 1% 1.5% 10% 50 mV 10 ms Phase PRCs calculated using XPPAUT (Ermentrout, 2002) LOW MEDIUM HIGH 75 26 26 24 24 50 % Phase Lag 23 22 20 20 25 18 18 16 16 14 14 0.1 0.1 11 10 10 % Active % Active 0 0 100 100 % Phase Lag 28 28 Intrinsic Frequency (Hz) Intrinsic Frequency (Hz) Predicted Network Dynamics Intrinsic Frequency % Phase Lag Weakly coupled oscillator theory used to define three different dynamic regions -LOW, MEDIUM, HIGH that refer to PRCs with particular characteristics (e.g., negative PRCs for MEDIUM) Phase lags determined from interaction functions calculated using XPPAUT (Ermentrout, 2002) Results Simulations confirm theoretical predictions 28 LOW MED HIGH 75 75 50 50 22 % Phase Lag Intrinsic Frequency (Hz) 24 25 20 25 18 % Phase Lag Intrinsic Frequency (Hz) % Phase Lag 26 Intrinsic Frequency % Phase Lag 0 16 14 0.1 0.1 11 10 10 0 100 100 % Active % Active •“Weak coupling” is about 10 pS (comparing predicted and simulated) • Compare full and reduced model phase lag values to “define” synchronous and asynchronous • Synchronous is 10% or less phase lag, asynchronous otherwise Cell 1: 15% basal attenuation, 2% apical attenuation Cell 2: 8% basal attenuation, 8% apical attenuation Cell 3: 6% basal attenuation, 14% apical attenuation apical apical CELL 3 basal basal Cell 1, apical coupling (multistability) Beyond weak coupling Beyond weak coupling Beyond weak coupling Discussion and Conclusions • PRC skewness quantifications can be used to predict whether synchronous or asynchronous modes occur in electrically coupled basket cells. • Averaged PRCs can be used to predict modes for coupling at multiple sites. • Predictions cannot be made under all circumstances and multistability can occur. • Different apical and basal attenuation (due to different channel densities) allow more ‘robust’ asynchrony to occur with coupling on the more attenuated dendritic side. • Network couplings that produce asynchrony (as compared to synchrony) with weak coupling encompass more dynamic richness (i.e., range of possible phase lags) with gap junction conductance changes. • Thus, gap junction coupling may be able to tune networks in and out of synchronous activities if asynchrony with weak coupling is predicted. the end • Thank you!