All events, 2012

Towards a link between hippocampal network dynamics and exploratory behavior

Lecture
Date:
Tuesday, August 28, 2012
Hour: 12:30
Location:
Gerhard M.J. Schmidt Lecture Hall
Dr. Anton Sirota
|
Centre for Integrative Neuroscience, Tubingen University, Germany

The role of phagocytic activity in brain maintenance

Lecture
Date:
Tuesday, August 14, 2012
Hour: 12:30
Location:
Gerhard M.J. Schmidt Lecture Hall
Prof. Jonathan Kipnis
|
Dept of Neuroscience, University of Virginia, Charlottesville VA

Thousands of new neurons are generated daily during adult life but only a fraction of them survive, mature and incorporate into the neural circuits; the rest die, and their corpses are presumably cleared by other healthy cells. How the dying neurons are removed and how such clearance influences neurogenesis are not well understood. We identified an unexpected phagocytic role for the doublecortin (DCX)-positive neuronal progenitor cells during adult neurogenesis. Our in vivo and ex vivo studies demonstrate that DCX+ cells comprise of a significant phagocytic population within the neurogenic zones. Intracellular engulfment protein ELMO1, which promotes Rac activation downstream of phagocytic receptors, was required for phagocytosis by DCX+ cells. Disruption of engulfment in vivo genetically (in Elmo1-null mice) or pharmacologically (in wild type mice) led to reduced uptake by DCX+ cells, accumulation of apoptotic nuclei in the neurogenic niches, and impaired neurogenesis. Implication of this phenomenon could be relevant to clinical conditions associated with induced (stroke) or impaired (depression) neurogenesis. We extended our studies of phagocytic activity to neurodevelopmental diseases, such as autistic spectrum disorders and Rett syndrome, in particular. We found that myeloid compartment of Rett mice is impaired in phagocytic activity. When myeloid compartment is replaced using bone marrow transplantation from wild-type bone marrow into Mecp2‒/y mice, the disease is arrested and life expectancy is increased by more than five-fold. Bone marrow transplantation results in engraftment of the brain parenchyma with wild type microglia-like cells, capable of clearing apoptotic debris load, which presumably allows more efficient neuronal function. Our data unexpectedly implicate myeloid cells in Rett pathology, and suggest that these immune cells might offer a feasible target for future therapeutic intervention for this devastating disease.

A Reconstruction of the Neocortical Column

Lecture
Date:
Tuesday, July 31, 2012
Hour: 10:00
Location:
Gerhard M.J. Schmidt Lecture Hall
Prof. Henry Markram
|
The Blue Brain Project, Ecole Polytechnique Fédérale de Lausanne, Switzerland

A multitude of experiments over the past century have yielded deep insights into the cellular and synaptic organization of the microcircuitry of the neocortex and its possible role as a functional unit - a column of cells across 6 layers. The available data is, however, not standardized, is highly fragmented and often conflicting. More importantly, there are large gaps in our knowledge requiring an impractical number of experiments to fill. We therefore developed a strategy to accelerate a comprehensive analysis of the neocortical column by attempting to reconstruct it from partial information. We performed a spectrum of standardized biological experiments on strategic cellular and synaptic properties of the microcircuitry of the somatosensory cortex of a young rat and gathered further relevant data from previously published studies. We developed a generic supercomputer-based platform to build and simulate biologically-detailed brain models, and attempted to reconstruct a first draft of a unifying model at the cellular level of detail. The model integrates and unifies most of the current data, significantly predicts missing data, and provides a broad range of new insights into the structural and functional organization of neocortical microcircuitry. The model also serves as a virtual specimen for a new generation of simulation-based experimentation that can accelerate an integrated understanding of the cellular and synaptic basis of neocortical function.

Perceptual bias induced by optical stimulation in the macaque frontal eye field

Lecture
Date:
Tuesday, July 24, 2012
Hour: 12:30
Location:
Nella and Leon Benoziyo Building for Brain Research
Dr. Shay Ohayon
|
Computation and Neural Systems CALTECH

We studied differences between optical and electrical micro-stimulation (MS) in the macaque frontal eye field (FEF) using single unit recordings, behavioral essay and fMRI. The frontal eye field serves as ideal test bed since it has been thoroughly characterized with electrical stimulation and because a behavioral effect (i.e. saccade) is easily induced by electrical MS. Three different constructs (AAV5-hSyn-eNpHR3.0, AAV5-hSyn-ChR2, AAV5-CAG-Arch) were injected to three FEF sites in two monkeys and robust firing rate modulations were observed upon light delivery. Although activity modulation was observed as far as 2mm away from the optical stimulation site, no significant voxel activation was found during combined fMRI and optical stimulation. High current electrical MS reliably induced saccades. Low current electrical MS combined with optical stimulation increased the probability of eliciting a saccade, suggesting optical stimulation may be similar to a low current electrical MS, known to induce an attentional bias. To test the possible effects of optical stimulation on attention monkeys were trained on a delayed memory saccade task. We observed significant changes in performance during optical stimulation trials, such as an increase in incorrect and missed trials, suggesting monkeys failed to perceive the instructed cue signal in the periphery.

Optogenetics symposium

Conference
Date:
Saturday, July 14, 2012
Hour:
Location:
The David Lopatie Conference Centre

90th Birthday Meeting for Prof. David Samuel

Conference
Date:
Thursday, June 28, 2012
Hour:
Location:
Michael Sela Auditorium

Homepage

Brain-to-brain coupling:a mechanism for creating and sharing a social world

Lecture
Date:
Thursday, June 21, 2012
Hour: 14:30
Location:
Nella and Leon Benoziyo Building for Brain Research
Prof. Uri Hasson
|
Dept of Psychology, Princeton University

Cognition materializes in an interpersonal space. The emergence of complex behaviors requires the coordination of actions among individuals according to a shared set of rules. Despite the central role of other individuals in shaping our minds, experiments typically isolate human or animal subjects from their natural environment by placing them in a sealed quiet room where interactions occur solely with a computer screen. In everyday life, however, we spend most of our time interacting with other individuals. In the talk I will argue in favor of a shift from a single-brain to a multi-brain frame of reference. I will present a series of studies aimed at characterizing the brain-to-brain coupling during real life social interaction. The data suggest that in many cases the neural processes in one brain are coupled to the neural processes in another brain via the transmission of a signal through the environment. The brain-to-brain neural coupling exposes a shared neural substrate that exhibits temporally aligned response patterns across communicators. The recording of the neural responses from two brains opens a new window into the neural basis of interpersonal communication, and may be used to assess verbal and non-verbal forms of interaction in both human and other model systems.

New solutions to the "solved" problem of how sodium channels control cortical neuronal excitability

Lecture
Date:
Tuesday, June 19, 2012
Hour: 12:30
Location:
Gerhard M.J. Schmidt Lecture Hall
Prof. Mike Gutnick
|
Veterinary Medicine, Faculty of Agriculture, Hebrew University of Jerusalem

60 years ago, Hodgkin and Huxley published their seminal papers which described the kinetics of voltage-gated ionic currents in the squid giant axon and used these measurements to produce the fundamental model of action potential generation. Their findings have become the basis for our understanding of neuronal excitability and information processing and are central to computational models of neuronal function. However, it turns out that the precise activation and inactivation characteristics of voltage-gated sodium channels in the CNS can vary widely, not only depending on the brain region, cell type and molecular subunit, but also as a function of the location of channels within the neuron and their relationship to the local membrane cytoskeleton. These differences in current properties can have a profound functional impact. I will discuss our data on transient and persistent sodium currents in the various compartments of the cortical pyramidal neuron, collected in brain slices using whole-cell current and on-cell single channel recordings and imaging of sodium-sensitive fluorescent dyes.

Parallel, non-convergent, interactions between separate cortical loci underlie perceptual unity: implications for a new view of object recognition

Lecture
Date:
Sunday, June 17, 2012
Hour: 12:30
Location:
Gerhard M.J. Schmidt Lecture Hall
Prof. Moshe Gur
|
Dept of Biomedical Engineering, Technion, Haifa

Any physical device, including computers, when comparing A to B, must send the information to point C. Explanations of brain processing take such a convergence for granted thus generating models relying on increasingly converging hierarchical streams. Such models, however, consistently fail to explain many perceptual phenomena. To see whether the brain, at times, can compare (integrate, process) events that take place at different loci without sending the information to a common target, I performed experiments in three modalities, somato-sensory, auditory, and visual, where 2 different loci at the primary cortex were stimulated. Subjects were able to integrate inputs in time and space affecting small separate cortical loci. The ability to correlate activity between loci was independent of cortical distance up to 2-4 cm. Given the organization of sensory cortex where localized responses in primary cortex do not interact while convergence in downstream areas results in loss of individual stimulus identity and in decreasing selectivity to elementary stimuli, those results cannot be explained by conventional convergence models. We must thus assume a non-converging mechanism whereby two (or more) activated cortical loci can be integrated without sending information via axons into another downstream integrating site. Once we allow for such a non-converging mechanism, many perceptual phenomena can be viewed differently. Object recognition and representation is such a phenomenon that, I suggest, does not result from hierarchical convergence of cells with ever-increasing feature selectivity but rather from parallel interactions between various visual and non-visual areas. If my hypothesis of the brain ability to relate activity taking place at separate loci without using convergence-by-wires is correct, it implies that the brain can use heretofore unconsidered (unknown?) parallel processing and that conventional models, including computer programs, would not be able to capture many brain processes.

Bird's Brain? Possible relations between behavior and brain plasticity

Lecture
Date:
Tuesday, June 12, 2012
Hour: 12:30
Location:
Gerhard M.J. Schmidt Lecture Hall
Prof. Anat Barnea
|
Dept of Natural and Life Sciences The Open University of Israel

Neurogenesis (birth of new neurons) occurs in many vertebrates, including humans. Most of the new neurons die before reaching destination. Those which survive migrate to various brain regions, replace older ones and connect to existing circuits. Evidence suggests that this replacement is related to acquisition of new information. Therefore, neuronal replacement is seen as a form of brain plasticity that enables organisms to adjust to environmental changes. However, direct evidence of a causal link between replacement and learning remains elusive. I will review a few of our studies which tried to uncover conditions that influence new neuronal recruitment and survival, and how these phenomena relate to the life of birds. The hypothesis is that an increase in new neuron recruitment is associated with expected or actual increase in memory load, particularly in brain regions that process and perhaps store this new information. Moreover, since new neuronal recruitment is part of a turnover process, we assume that the same conditions that favor the survival of some neurons induce the death of others. I will offer a frame and rational for comparing neuronal replacement in the adult avian brain, and try to uncover the pressures, rules, and mechanisms that govern its constant rejuvenation. I will discuss a variety of behaviors and environmental conditions (especially birds' migration, and if time permits - parent-offspring recognition) and their effect on new neuronal recruitment in relevant regions in the avian brain. I will describe various approaches and techniques which we used in those studies (behavioral, anatomical, cellular and hormonal), and will emphasize the significance of studying behavior and brain function under natural or naturalistic conditions.

Pages

All events, 2012

The role of phagocytic activity in brain maintenance

Lecture
Date:
Tuesday, August 14, 2012
Hour: 12:30
Location:
Gerhard M.J. Schmidt Lecture Hall
Prof. Jonathan Kipnis
|
Dept of Neuroscience, University of Virginia, Charlottesville VA

Thousands of new neurons are generated daily during adult life but only a fraction of them survive, mature and incorporate into the neural circuits; the rest die, and their corpses are presumably cleared by other healthy cells. How the dying neurons are removed and how such clearance influences neurogenesis are not well understood. We identified an unexpected phagocytic role for the doublecortin (DCX)-positive neuronal progenitor cells during adult neurogenesis. Our in vivo and ex vivo studies demonstrate that DCX+ cells comprise of a significant phagocytic population within the neurogenic zones. Intracellular engulfment protein ELMO1, which promotes Rac activation downstream of phagocytic receptors, was required for phagocytosis by DCX+ cells. Disruption of engulfment in vivo genetically (in Elmo1-null mice) or pharmacologically (in wild type mice) led to reduced uptake by DCX+ cells, accumulation of apoptotic nuclei in the neurogenic niches, and impaired neurogenesis. Implication of this phenomenon could be relevant to clinical conditions associated with induced (stroke) or impaired (depression) neurogenesis. We extended our studies of phagocytic activity to neurodevelopmental diseases, such as autistic spectrum disorders and Rett syndrome, in particular. We found that myeloid compartment of Rett mice is impaired in phagocytic activity. When myeloid compartment is replaced using bone marrow transplantation from wild-type bone marrow into Mecp2‒/y mice, the disease is arrested and life expectancy is increased by more than five-fold. Bone marrow transplantation results in engraftment of the brain parenchyma with wild type microglia-like cells, capable of clearing apoptotic debris load, which presumably allows more efficient neuronal function. Our data unexpectedly implicate myeloid cells in Rett pathology, and suggest that these immune cells might offer a feasible target for future therapeutic intervention for this devastating disease.

A Reconstruction of the Neocortical Column

Lecture
Date:
Tuesday, July 31, 2012
Hour: 10:00
Location:
Gerhard M.J. Schmidt Lecture Hall
Prof. Henry Markram
|
The Blue Brain Project, Ecole Polytechnique Fédérale de Lausanne, Switzerland

A multitude of experiments over the past century have yielded deep insights into the cellular and synaptic organization of the microcircuitry of the neocortex and its possible role as a functional unit - a column of cells across 6 layers. The available data is, however, not standardized, is highly fragmented and often conflicting. More importantly, there are large gaps in our knowledge requiring an impractical number of experiments to fill. We therefore developed a strategy to accelerate a comprehensive analysis of the neocortical column by attempting to reconstruct it from partial information. We performed a spectrum of standardized biological experiments on strategic cellular and synaptic properties of the microcircuitry of the somatosensory cortex of a young rat and gathered further relevant data from previously published studies. We developed a generic supercomputer-based platform to build and simulate biologically-detailed brain models, and attempted to reconstruct a first draft of a unifying model at the cellular level of detail. The model integrates and unifies most of the current data, significantly predicts missing data, and provides a broad range of new insights into the structural and functional organization of neocortical microcircuitry. The model also serves as a virtual specimen for a new generation of simulation-based experimentation that can accelerate an integrated understanding of the cellular and synaptic basis of neocortical function.

Perceptual bias induced by optical stimulation in the macaque frontal eye field

Lecture
Date:
Tuesday, July 24, 2012
Hour: 12:30
Location:
Nella and Leon Benoziyo Building for Brain Research
Dr. Shay Ohayon
|
Computation and Neural Systems CALTECH

We studied differences between optical and electrical micro-stimulation (MS) in the macaque frontal eye field (FEF) using single unit recordings, behavioral essay and fMRI. The frontal eye field serves as ideal test bed since it has been thoroughly characterized with electrical stimulation and because a behavioral effect (i.e. saccade) is easily induced by electrical MS. Three different constructs (AAV5-hSyn-eNpHR3.0, AAV5-hSyn-ChR2, AAV5-CAG-Arch) were injected to three FEF sites in two monkeys and robust firing rate modulations were observed upon light delivery. Although activity modulation was observed as far as 2mm away from the optical stimulation site, no significant voxel activation was found during combined fMRI and optical stimulation. High current electrical MS reliably induced saccades. Low current electrical MS combined with optical stimulation increased the probability of eliciting a saccade, suggesting optical stimulation may be similar to a low current electrical MS, known to induce an attentional bias. To test the possible effects of optical stimulation on attention monkeys were trained on a delayed memory saccade task. We observed significant changes in performance during optical stimulation trials, such as an increase in incorrect and missed trials, suggesting monkeys failed to perceive the instructed cue signal in the periphery.

Brain-to-brain coupling:a mechanism for creating and sharing a social world

Lecture
Date:
Thursday, June 21, 2012
Hour: 14:30
Location:
Nella and Leon Benoziyo Building for Brain Research
Prof. Uri Hasson
|
Dept of Psychology, Princeton University

Cognition materializes in an interpersonal space. The emergence of complex behaviors requires the coordination of actions among individuals according to a shared set of rules. Despite the central role of other individuals in shaping our minds, experiments typically isolate human or animal subjects from their natural environment by placing them in a sealed quiet room where interactions occur solely with a computer screen. In everyday life, however, we spend most of our time interacting with other individuals. In the talk I will argue in favor of a shift from a single-brain to a multi-brain frame of reference. I will present a series of studies aimed at characterizing the brain-to-brain coupling during real life social interaction. The data suggest that in many cases the neural processes in one brain are coupled to the neural processes in another brain via the transmission of a signal through the environment. The brain-to-brain neural coupling exposes a shared neural substrate that exhibits temporally aligned response patterns across communicators. The recording of the neural responses from two brains opens a new window into the neural basis of interpersonal communication, and may be used to assess verbal and non-verbal forms of interaction in both human and other model systems.

New solutions to the "solved" problem of how sodium channels control cortical neuronal excitability

Lecture
Date:
Tuesday, June 19, 2012
Hour: 12:30
Location:
Gerhard M.J. Schmidt Lecture Hall
Prof. Mike Gutnick
|
Veterinary Medicine, Faculty of Agriculture, Hebrew University of Jerusalem

60 years ago, Hodgkin and Huxley published their seminal papers which described the kinetics of voltage-gated ionic currents in the squid giant axon and used these measurements to produce the fundamental model of action potential generation. Their findings have become the basis for our understanding of neuronal excitability and information processing and are central to computational models of neuronal function. However, it turns out that the precise activation and inactivation characteristics of voltage-gated sodium channels in the CNS can vary widely, not only depending on the brain region, cell type and molecular subunit, but also as a function of the location of channels within the neuron and their relationship to the local membrane cytoskeleton. These differences in current properties can have a profound functional impact. I will discuss our data on transient and persistent sodium currents in the various compartments of the cortical pyramidal neuron, collected in brain slices using whole-cell current and on-cell single channel recordings and imaging of sodium-sensitive fluorescent dyes.

Parallel, non-convergent, interactions between separate cortical loci underlie perceptual unity: implications for a new view of object recognition

Lecture
Date:
Sunday, June 17, 2012
Hour: 12:30
Location:
Gerhard M.J. Schmidt Lecture Hall
Prof. Moshe Gur
|
Dept of Biomedical Engineering, Technion, Haifa

Any physical device, including computers, when comparing A to B, must send the information to point C. Explanations of brain processing take such a convergence for granted thus generating models relying on increasingly converging hierarchical streams. Such models, however, consistently fail to explain many perceptual phenomena. To see whether the brain, at times, can compare (integrate, process) events that take place at different loci without sending the information to a common target, I performed experiments in three modalities, somato-sensory, auditory, and visual, where 2 different loci at the primary cortex were stimulated. Subjects were able to integrate inputs in time and space affecting small separate cortical loci. The ability to correlate activity between loci was independent of cortical distance up to 2-4 cm. Given the organization of sensory cortex where localized responses in primary cortex do not interact while convergence in downstream areas results in loss of individual stimulus identity and in decreasing selectivity to elementary stimuli, those results cannot be explained by conventional convergence models. We must thus assume a non-converging mechanism whereby two (or more) activated cortical loci can be integrated without sending information via axons into another downstream integrating site. Once we allow for such a non-converging mechanism, many perceptual phenomena can be viewed differently. Object recognition and representation is such a phenomenon that, I suggest, does not result from hierarchical convergence of cells with ever-increasing feature selectivity but rather from parallel interactions between various visual and non-visual areas. If my hypothesis of the brain ability to relate activity taking place at separate loci without using convergence-by-wires is correct, it implies that the brain can use heretofore unconsidered (unknown?) parallel processing and that conventional models, including computer programs, would not be able to capture many brain processes.

Bird's Brain? Possible relations between behavior and brain plasticity

Lecture
Date:
Tuesday, June 12, 2012
Hour: 12:30
Location:
Gerhard M.J. Schmidt Lecture Hall
Prof. Anat Barnea
|
Dept of Natural and Life Sciences The Open University of Israel

Neurogenesis (birth of new neurons) occurs in many vertebrates, including humans. Most of the new neurons die before reaching destination. Those which survive migrate to various brain regions, replace older ones and connect to existing circuits. Evidence suggests that this replacement is related to acquisition of new information. Therefore, neuronal replacement is seen as a form of brain plasticity that enables organisms to adjust to environmental changes. However, direct evidence of a causal link between replacement and learning remains elusive. I will review a few of our studies which tried to uncover conditions that influence new neuronal recruitment and survival, and how these phenomena relate to the life of birds. The hypothesis is that an increase in new neuron recruitment is associated with expected or actual increase in memory load, particularly in brain regions that process and perhaps store this new information. Moreover, since new neuronal recruitment is part of a turnover process, we assume that the same conditions that favor the survival of some neurons induce the death of others. I will offer a frame and rational for comparing neuronal replacement in the adult avian brain, and try to uncover the pressures, rules, and mechanisms that govern its constant rejuvenation. I will discuss a variety of behaviors and environmental conditions (especially birds' migration, and if time permits - parent-offspring recognition) and their effect on new neuronal recruitment in relevant regions in the avian brain. I will describe various approaches and techniques which we used in those studies (behavioral, anatomical, cellular and hormonal), and will emphasize the significance of studying behavior and brain function under natural or naturalistic conditions.

From discrete elements to a perceived contour in the primary visual cortex

Lecture
Date:
Tuesday, June 5, 2012
Hour: 12:30
Location:
Gerhard M.J. Schmidt Lecture Hall
Dr. Hamutal Slovin
|
Gonda Brain Research Center Bar Ilan University

The neuronal mechanisms underlying perceptual grouping of discrete, similarly oriented elements are not well understood. To investigate this, we imaged population responses in V1 of monkeys trained on a contour detection task. Mapping neuronal populations processing contour/background elements in V1 enabled studying the role of two encoding mechanisms: strength of population response and synchronization. Response maps early in time showed activation patches corresponding to the contour/background individual elements. An early increased synchronization between the contour elements, accompanied by decreased synchronization between the background elements, suggested that contour integration is initiated with synchronization changes. However only response modulation at later times, defined by increased activity in the contour elements, along with suppressed activity in the background elements, enabled to visualize in single trials, a salient continuous contour segregated from a noisy background. Finally, the late modulation was correlated with psychophysical performance of contour saliency, further supporting its role in contour perception. In the second part of this talk we will demonstrate the effects of microsaccades on perceptual mechanisms in V1.

Creating a nuisance to probe the neural code

Lecture
Date:
Tuesday, May 29, 2012
Hour: 12:30
Location:
Gerhard M.J. Schmidt Lecture Hall
Dr. Mickey London
|
Edmond and Lily Safra Center for Brain Sciences The Hebrew University of Jerusalem

A major objective of neuroscience is to understand the neural code, namely how the patterns of neuronal signals (e.g. action potentials, membrane potential, calcium concentrations) “represent” physical objects, commands for actions, or psychological phenomena. An successful neural coding scheme has to be robust to noise (i.e. random neuronal activity). We have recently shown that using a small perturbation, an introduction of one “extra”-spike to the activity of a single neuron in the cortex, and studying the consequence of that perturbation we can obtain bounds on the level of noise in the cortex. Theoretical analysis of the data indicates that intrinsic, stimulus-independent variations in membrane potential of cortical neurons are on the order of 2.2–4.5 mV—variations that are pure noise, and so carry no information at all. Such level of noise places severe limitations on the plausibility of neural code based on precise spike timing. Using recent advances in optogentics we can extend the approach of introducing a precisely controlled perturbation. We explore how these perturbations affect the dynamics of activity in the cortex as well as theirs effect on animal performance on a task, to gain further bounds and insights on the neural code.

Creating a nuisance to probe the neural code

Lecture
Date:
Tuesday, May 29, 2012
Hour: 12:30
Location:
Gerhard M.J. Schmidt Lecture Hall
Dr. Mickey London
|
Edmond and Lily Safra Center for Brain Sciences The Hebrew University of Jerusalem

A major objective of neuroscience is to understand the neural code, namely how the patterns of neuronal signals (e.g. action potentials, membrane potential, calcium concentrations) “represent” physical objects, commands for actions, or psychological phenomena. An successful neural coding scheme has to be robust to noise (i.e. random neuronal activity). We have recently shown that using a small perturbation, an introduction of one “extra”-spike to the activity of a single neuron in the cortex, and studying the consequence of that perturbation we can obtain bounds on the level of noise in the cortex. Theoretical analysis of the data indicates that intrinsic, stimulus-independent variations in membrane potential of cortical neurons are on the order of 2.2–4.5 mV—variations that are pure noise, and so carry no information at all. Such level of noise places severe limitations on the plausibility of neural code based on precise spike timing. Using recent advances in optogentics we can extend the approach of introducing a precisely controlled perturbation. We explore how these perturbations affect the dynamics of activity in the cortex as well as theirs effect on animal performance on a task, to gain further bounds and insights on the neural code.

Pages

All events, 2012

There are no events to display

All events, 2012

There are no events to display