H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – 27-28 OCT 2011 - 1 Project-Team BEAGLE INRIA Rhône-Alpes LIRIS UMR CNRS 5205 Université.

Slides:



Advertisements
Similar presentations
Synaptic Homeostasis Sean Sweeney Module 725. mEPSPs are recordings of release of one vesicle/quantum. EPSP is a suprathreshold stimulation Of the nerve.
Advertisements

Long-term Potentiation as a Physiological Phenomenon
Justin Besant BIONB 2220 Final Project
Spike Timing-Dependent Plasticity Presented by: Arash Ashari Slides mostly from: 1  Woodin MA, Ganguly K, and Poo MM. Coincident pre-
Part III: Models of synaptic plasticity BOOK: Spiking Neuron Models, W. Gerstner and W. Kistler Cambridge University Press, 2002 Chapters Laboratory.
Spike timing-dependent plasticity: Rules and use of synaptic adaptation Rudy Guyonneau Rufin van Rullen and Simon J. Thorpe Rétroaction lors de l‘ Intégration.
Spike timing dependent plasticity Homeostatic regulation of synaptic plasticity.
Spike timing-dependent plasticity Guoqiang Bi Department of Neurobiology University of Pittsburgh School of Medicine.
Synaptic Plasticity.
Figure 8.1 Forms of short-term synaptic plasticity.
Plasticity in the nervous system Edward Mann 17 th Jan 2014.
Lecture 14: The Biology of Learning References: H Shouval, M F Bear, L N Cooper, PNAS 99, (2002) H Shouval, G Castellani, B Blais, L C Yeung,
Real Neurons for Engineers (Lecture 2) Harry R. Erwin, PhD COMM2E University of Sunderland.
Before we start: What is the question? Why is it interesting?
Synapses are everywhere neurons synapses Synapse change continuously –From msec –To hours (memory) Lack HH type model for the synapse.
Long term potentiation (LTP) of an excitatory synaptic inputs is input specific.
A globally asymptotically stable plasticity rule for firing rate homeostasis Prashant Joshi & Jochen Triesch
Bi/CNS 150 Lecture 20 Friday November 15, 2014 Learning & Memory 1. Synaptic plasticity Bruce Cohen Kandel,Chap. 12: pp , Chap
How facilitation influences an attractor model of decision making Larissa Albantakis.
1 Activity-dependent Development (2) Hebb’s hypothesis Hebbian plasticity in visual system Cellular mechanism of Hebbian plasticity.
Critical periods A time period when environmental factors have especially strong influence in a particular behavior. –Language fluency –Birds- Are you.
Copyright © 2007 Wolters Kluwer Health | Lippincott Williams & Wilkins Neuroscience: Exploring the Brain, 3e Chapter 25: Molecular Mechanisms of Learning.
Synaptic plasticity Basic Neuroscience NBL 120. classical conditioning CS (neutral) - no response US - UR After pairing: CS - CR.
Neural Plasticity Lecture 7. Neural Plasticity n Nervous System is malleable l learning occurs n Structural changes l increased dendritic branching l.
Biological Modeling of Neural Networks Week 4 – Reducing detail - Adding detail Wulfram Gerstner EPFL, Lausanne, Switzerland 4.2. Adding detail - synapse.
Learning and Stability. Learning and Memory Ramón y Cajal, 19 th century.
Biological Modeling of Neural Networks: Week 14 – Dynamics and Plasticity Wulfram Gerstner EPFL, Lausanne, Switzerland 14.1 Reservoir computing - Complex.
Molecular mechanisms of memory. How does the brain achieve Hebbian plasticity? How is the co-activity of presynaptic and postsynaptic cells registered.
Neural Plasticity: Long-term Potentiation Lesson 15.
HEBB’S THEORY The implications of his theory, and their application to Artificial Life.
synaptic plasticity is the ability of the connection, or synapse, between two neurons to change in strength in response to either use or disuse of transmission.
Optical approaches to synaptic plasticity: From unitary events to learning rules Sam Wang Princeton University.
Biological Modeling of Neural Networks Week 6 Hebbian LEARNING and ASSOCIATIVE MEMORY Wulfram Gerstner EPFL, Lausanne, Switzerland 6.1 Synaptic Plasticity.
Unit 4 Psychology Learning: Neural Pathways, Synapse Formation & the Role of Neurotransmitters.
A Calcium dependent model of synaptic plasticity (CaDp)
Spike-timing-dependent plasticity (STDP) and its relation to differential Hebbian learning.
Mechanisms for memory: Introduction to LTP Bailey Lorv Psych 3FA3 November 15, 2010.
”When spikes do matter: speed and plasticity” Thomas Trappenberg 1.Generation of spikes 2.Hodgkin-Huxley equation 3.Beyond HH (Wilson model) 4.Compartmental.
1 7. Associators and synaptic plasticity Lecture Notes on Brain and Computation Byoung-Tak Zhang Biointelligence Laboratory School of Computer Science.
Synaptic plasticity: Introduction Different induction protocols Basic properties Key elements of the biophysics Site of change: pre or post-synaptic More.
1 4. Associators and Synaptic Plasticity Lecture Notes on Brain and Computation Byoung-Tak Zhang Biointelligence Laboratory School of Computer Science.
Strong claim: Synaptic plasticity is the only game in town. Weak Claim: Synaptic plasticity is a game in town. Biophysics class: section III The synaptic.
Synaptic plasticity DENT/OBHS 131 Neuroscience 2009.
Slide 1 Neuroscience: Exploring the Brain, 3rd Ed, Bear, Connors, and Paradiso Copyright © 2007 Lippincott Williams & Wilkins Bear: Neuroscience: Exploring.
Trends in Biomedical Science Making Memory. The following slides are mostly derived from The Brain from Top to Bottom, an Interactive Website about the.
Copyright © 2004 Allyn and Bacon 1 Chapter 13 Learning and Memory: Basic Mechanisms This multimedia product and its contents are protected under copyright.
Synaptic plasticity. Definition Alteration of synapse response to input.
1 Bi/CNS 150 Lecture 21 Friday November 15, 2012 Learning & Memory 1. Synaptic plasticity Henry Lester Chapter 63 (from p 1258)
Learning & Memory 2. Synaptic plasticity
Neural Mechanisms of Learning & Memory Lesson 24.
Keeping the neurons cool Homeostatic Plasticity Processes in the Brain.
APPROACHES TO THE BIOLOGY OF MEMORY Scale of analysis: –Micro: intra, intercellular –Medio: cell assemblies and neural networks –Macro: Coordinated brain.
0 Chapter 4: Associators and synaptic plasticity Fundamentals of Computational Neuroscience Dec 09.
Perceptron vs. the point neuron Incoming signals from synapses are summed up at the soma, the biological “inner product” On crossing a threshold, the cell.
Synaptic Plasticity Synaptic efficacy (strength) is changing with time. Many of these changes are activity-dependent, i.e. the magnitude and direction.
Week 6 Hebbian LEARNING and ASSOCIATIVE MEMORY Wulfram Gerstner EPFL, Lausanne, Switzerland 6.1 Synaptic Plasticity - Hebbian Learning - Short-term Plasticity.
CS 2016 Long-Term Synaptic Plasticity III Christian Stricker ANUMS/JCSMR - ANU
Ch 8. Synaptic Plasticity 8.9 ~ 8.10 Adaptive Cooperative Systems, Martin Beckerman, Summarized by Kim, S. –J. Biointelligence Laboratory, Seoul.
Spike-timing-dependent plasticity (STDP) and its relation to differential Hebbian learning.
Synaptic Plasticity and the NMDA Receptor
Types of Learning Associative Learning: Classical Conditioning
Section 2 Interaction between neurons
Capacity of auto-associative networks
Types of Learning Associative Learning: Classical Conditioning
Types of Learning Associative Learning: Classical Conditioning
Types of Memory (iconic memory) (7 bits for 30seconds)
Kaushik Majumdar Center for Complex Systems and Brain Sciences
Types of Learning Associative Learning: Classical Conditioning
Spike-timing-dependent plasticity (STDP)
Neuroscience: Exploring the Brain, 3e
Presentation transcript:

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Project-Team BEAGLE INRIA Rhône-Alpes LIRIS UMR CNRS 5205 Université de Lyon, France DevLeaNN - Paris – OCT 201 Hugues BERRY Unconventional forms of plasticity: beyond the synaptic Hebbian paradigm

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Origin of synaptic plasticity: Donald Hebb 1949, Hebb's PhD Thesis: " When an axon of cell A [...] persistently takes part in firing cell B, some growth process or metabolic change takes place in one or both cells such that A's efficiency, as one of the cells firing B, is increased " Major points: –long-lasting changes (trace, memory) –associativity (A & B must both fire) –locality (depends only on A & B) Major issue: can only increase

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Evidence for long-term potentiation (LTP) Came out in the early 1970's (Bliss & Lomo J Physiol 1973) High Frequency stimulations (HFS) in the hippocampus maintains for hours-days A B From Fino et al. J Neurosci 2005 ≈200 pulses ≈100 Hz stimulation

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Evidence for long-term depression (LTD) Came out in the early 1990's (Dudek & Bear PNAS 1992) Low Frequency stimulations (LFS) in the hippocampus From Fino et al. J Neurosci 2005 maintains for hours-days A B ≈1000 pulses ≈1 Hz stimulation

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Transition to spikes and spike-timings Initiated in late 1990's ( Markram et al. Science 1997; Bi & Poo J Neurosci 1998) LTP or LTD depending on the timing between pairs of post- and pre- synaptic spikes A (pre) B (post) pre post pre post Δt = t post -t pre < 0Δt = t post -t pre > 0 Bi & Poo J Neurosci 1998 maintains for hours ≈100 paired ≈1 Hz ΔtΔt pre post 1 s stimulation

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Molecular basis glutamate synapses) from Citri & Malenka Neuropsychopharmacology 2008 V soma (mV) time V rest V thr tAtA tAtA tAtA tBtB  LTP  LTD

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Is that all our brain does? Most computational models with plastic / learning synapses use rules derived from Hebbian LTP/LTD or STDP. Yet there is more than this going on in our brains: – Anti-Hebbian plasticity

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Is that all our brain does? Most computational models with plastic / learning synapses use rules derived from Hebbian LTP/LTD or STDP. Yet there is more than this going on in our brains: – Anti-Hebbian plasticity – Relaxed locality Neuromodulation (e.g. dopamine, serotonin) Glia-neuron interactions

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Is that all our brain does? Most computational models with plastic / learning synapses use rules derived from Hebbian LTP/LTD or STDP. Yet there is more than this going on in our brains: – Anti-Hebbian plasticity – Relaxed locality Neuromodulation (e.g. dopamine, serotonin) Glia-neuron interactions – Nonassociative rules : synaptic scaling short-term facilitation

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Is that all our brain does? Most computational models with plastic / learning synapses use rules derived from Hebbian LTP/LTD or STDP. Yet there is more than this going on in our brains: – Anti-Hebbian plasticity – Relaxed locality Neuromodulation (e.g. dopamine, serotonin) Glia-neuron interactions – Nonassociative rules : synaptic scaling short-term facilitation – Intrinsic plasticity

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Outline STDP: evolution with the number of paired stimulations Intrinsic long-term plasticity of the threshold or gain –mechanical origins –competition with synaptic Hebbian learning in chaotic recurrent networks Short term plasticity –modulation by glial cells: the tripartite synapse

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT STDP : EVOLUTION WITH THE NUMBER OF PAIRED STIMULATIONS WITH B. DELORD AND L. VENANCE LABS

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT STDP in the basal ganglia BG = motor control, procedural memory, goal oriented tasks. The striatum is the major input nucleus for cortical input from Fino & Venance Front Synaptic Neurosci 2010 cortico-striatal synapses

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT STDP in the basal 100 stims STDP in at cortico-striatal synapses is Anti-Hebbian synaptic weight Fino et al. J Neurosci 2005 ≈100 paired pulses, ≈1 Hz ΔtΔt pre post 1 s Δt = t post -t pre < 0Δt = t post -t pre > 0 pre post pre post stimulation Bi & Poo J Neurosci 1998

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Decreasing the paired stimulation count Cui et al., submitted

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT LTP re-emerges at low stim. counts: model Cui et al., submitted signaling by AMPAR and NMDAR Retrograde signaling by endocannabinoids

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Low-stims LTP is endocannabinoid (eCB) Cui et al., submitted Full Model eCB-KO Model Experimental confirmation

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT eCB-Low stims LTP also exists in the cortex Cui et al., submitted

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT A novel form of LTP "Classical" NMDAR-mediated LTP and LTD disappear with fewer stimulations But an endocannabinoid-mediated LTP emerges for 5-20 pairings First evidence for endocannabinoid-mediated potentiation Ongoing work: –variations of the frequency and stochasticity of Δt –effects in a network (# stims, time scales) A possible cellular support for rapid learning: –Associative memories and behavioral rules can be learned within a few or even a single trial (Pasupathy et al. Nature 2005; Tse et al. Science 2007). –This would represent as few as 2-50 spikes – eCB-low stims LTP may code such rapid learnings

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT INTRINSIC PLASTICITY OF THE THRESHOLD OR GAIN WITH B. DELORD LAB

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Plasticity of the f-I curve in the cortex firing frequency f Injected current I "Transfert function" Paz et al. J Physiol 2009

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Plasticity of the f-I curve in the cortex firing frequency f Injected current I "Transfert function" Paz et al. J Physiol 2009 stimulation

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Plasticity of the f-I curve in the cortex No change in synaptic weights : INTRINSIC PLASTICITY Paz et al. J Physiol 2009

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Modulations of voltage-gated channels What happense if other voltage-dependent ionic channels (ie not synaptic AMPAR and NMDAR) are also modulated by neural activity? Synaptic plasticity I NMDA I AMPA

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT generic voltage-gated ion channel X A generic Hodgkin-Huxley model leakspikeinjected current (soma) 0 injected current I inj Firing frequency of the neuron f Naudé et al., submitted g X = total quantity of X: ?? I X properties 1/

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Increasing g X changes the f-I Naudé et al., submitted IP expected with modulation of stiff- activating channels Channels activating before spike: plasticity of the f-I threshold θ Channels activating at or after spike: plasticity of the f-I inverse slope ε

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Homeostatic IP of the threshold A single neuron with Homeostatic IP of the threshold firing frequency f i Input of neuron i Input from the reservoir 0 firing frequency Naudé et al., submitted Desaturation of neuron i

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT H-IP of the threshold in mixed networks Recurrent neural networks (firing rate) with initial chaotic dynamics + Hebbian synaptic learning (Siri et al. J Physiol 2007; Neural Computation 2008) +/- H-IP of the threshold ? Network-averaged firing Network 10 3 learning steps SP (no IP) SP+IP Largest Lyapunov exponent Learning steps Naudé et al., submitted chaotic non chaotic

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT H-IP of the threshold in mixed networks Functional property: sensitivity to the input : Δ[x] = [network dynamics w/ input - network dynamics w/o input] Naudé et al., submitted SP (no IP) SP+IP Learning steps Δ[x] Network-averaged firing

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT H-IP of the threshold in mixed networks Functional property: sensitivity to the input : Δ[x] = [network dynamics w/ input - network dynamics w/o input] Naudé et al., submitted SP (no IP) SP+IP Learning steps Δ[x] SP+IP Network-averaged firing

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Conclusions Intrinsic plasticity – is to be expected when the number of stiff-activating voltage- dependent ionic channels is regulated by the neuron activity –nature of changes (θ or ε) depends on if the channel opens before or during the spike. – H-IP may prevents some of the runaway effects of synaptic plasticity (neuronal saturation, simplification of dynamics) Ongoing work –Non-homeostatic IP ? + - -

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT MODULATION OF SHORT-TERM PLASTICITY BY GLIAL CELLS WITH E. BEN JACOB LAB

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Short-term plasticity (STP) Recycling glutamate takes time: τ rec ≈ sec Restoring basal Ca levels after a presyn spike takes time: τ f ≈ 1-2 sec Maintains short-term only (0.1 – few sec) STP crucially conditions information transfert from pre to post (Tsodyks & Markram PNAS 1997; Abbott et al Science 1997) Ca 2+ + glutamate presyn spike frequency synaptic weight (% control) facilitation depression 100 Paired-pulse plasticity

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Glial cells modulate STP Glial cells (astrocytes) ≈ 50 % of human brain Not only mechanical/feeding support to neurons: –communicate with each other over long distances through slow calcium waves ( Goldberg et al. PLoS Comp Biol 2010; De Pittà et al. J Biol Phys 2009 ) – associate with synapses into tripartite synapses –bidirectional comunication between presynaptic, postynaptic and astrocytes Modulation of STP by glial cells has been evidenced but confusing: facilitation, depression, or both (Robitaille Neuron 1998; Jourdain et al., Nature Neurosci 2007) ? Haydon Nature Rev Neurosci 2001

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT A model of glia-modulated STP De Pitta et al. PLoS Comp Biol 2011

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Mean-field theory of the system De Pitta et al. PLoS Comp Biol 2011 syn. weight potentiation depression

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT syn. weight Confirmation by simulations De Pitta et al. PLoS Comp Biol 2011 = =

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Conclusion Astrocytes dynamically switch synapses between depressing and potentiating modes Astrocytes can decrease global synaptic weight while increasing paired-pulse potentiation (and vice-versa) (cf Jourdain et al., Nature Neurosci 2007) The plasticity characteristics of a synapse may not be fixed but could be modulated by associated astrocytes. Ongoing work: –effect on the postsynaptic terminal –modulation of long-term plasticity (STDP) Perspectives: assembly of a mixed glia/neuron network neuron glia ≈10 m/s ≈10 µm/s

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT SUMMARY

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Unconventional plasticity The "Unconventional computation" CS community: –"enrich or go beyond the standard models, such as the von-Neumann computer architecture and the Turing machine, which have dominated computer science for more than half a century" Unconventional plasticity: even though the synaptic Hebbian framework prevails, outside-the-box plasticity forms do exist and it may be worth looking at them for learning & memory. Expands the (limited?) framework of Hebbian synaptic plasticity: –time-scale-dependent plasticity ("quick learning" LTP) –homeostatic maintenance of dynamic regimes (intrinsic plasticity) –dynamic modulation of the synaptic operating regime (depressing/potentiating)

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Thanks!!! Funding : INSERM U1050 Collège de France, Paris Y. Cui E. Fino L. Venance ISIR, Univ P&M Curie, Paris France J. Naudé B. Delord S. Genet Contributions: for computer ressources Sch. Physics & Astronomy, Tel Aviv Univ, Israel M. Goldberg M. De Pittà E. Ben Jacob Project-Team Beagle, INRIA, Lyon, France J. Lallouette J.M. Gomès H. Berry Salk Institute, San Diego, USA V. Volman

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT More information 2011 Meeting of the Society for Neuroscience (Washington, Nov ) –"Sub-second induction unveils a switch from NMDA- to endocannabinoid-LTP", abstract # –"Astrocyte regulation of presynaptic plasticity", abstract # Published paper: –De Pittà, Volman, Berry & Ben Jacob (2011) A tale of two stories: astrocyte regulation of synaptic depression and facilitation, PLoS Comput Biol (in press). Questions?

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Is that all our brain does? Most computational models with plastic / learning synapses use rules derived from Hebbian LTP/LTD or STDP. Yet there is more than this going on in our brains: – Anti-Hebbian plasticity: – Relaxed locality Neuromodulation (e.g. dopamine, serotonin) Glia-neuron interactions – Nonassociative rules : synaptic scaling short-term facilitation A1 B A2 A1+A2=3 A1/A2=1/3 LTP A1+A2=6 A1/A2=2 Scaling A1+A2=3 A1/A2=2

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Short-term plasticity (STP) Recycling glutamate takes time: τ rec ≈ sec Restoring basal Ca levels after a presyn spike takes time: τ f ≈ 1-2 sec Maintains short-term only (0.1 – few sec) Ca 2+ + glutamate time presyn spikes presyn Ca postsyn potential τfτf

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Short-term plasticity (STP) Recycling glutamate takes time: τ rec ≈ sec Restoring basal Ca levels after a presyn spike takes time: τ f ≈ 1-2 sec Maintains short-term only (0.1 – few sec) Ca 2+ + glutamate time presyn spikes presyn Ca postsyn potential τfτf potentiation (facilitation)

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Short-term plasticity (STP) Recycling glutamate takes time: τ rec ≈ sec Restoring basal Ca levels after a presyn spike takes time: τ f ≈ 1-2 sec Maintains short-term only (0.1 – few sec) Ca 2+ + glutamate time presyn spikes presyn Ca postsyn potential τ rec depression

H. BERRY - Unconventional forms of plasticityDevLeaNN - Paris – OCT Short-term plasticity (STP) STP crucially conditions information transfert from pre to post (Tsodyks & Markram PNAS 1997; Abbott et al Science 1997) Ca 2+ + glutamate presyn spike frequency synaptic weight (% control) facilitation depression 100