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Full humanisation of the mouse immunoglobulin loci
Lecture
Thursday, August 25, 2016
Hour: 10:00
Location:
Wolfson Building for Biological Research
Full humanisation of the mouse immunoglobulin loci
Prof. Allan Bradley
Kymab, Cambridge MA
Professor Bradley is internationally recognized as a pioneer in developing the techniques, technology and tools for genetic manipulation in the mouse over more than 3 decades. He served as Director of the Welcome Trust Sanger Institute from 2000 to 2010. He was honored by election to the fellowship of the Royal Society in 2002. Among many projects that Dr. Bradley has established and led, is the international project to systematically knockout all genes in the mouse genome, the most ambitious use of ES-cell technology ever attempted. Over the last 30 years, Dr. Bradley has authored more than 280 publications. In his lecture, Dr. Bradley will be describing the scientific history and the technology behind the creation of the Kymouse strains which are transgenic for the total human immunoglobulin gene diversity. The platform provides a valuable means to isolate therapeutic monoclonal antibodies. Kymab has also developed single B cell-based methods to capture both the heavy and light chains of antibodies at scale. Combined with deep sequencing of millions of B cells we are able to build networks of histories of B cell families which we use to isolate rare antibodies with unique properties. The combined use of Kymouse with B cell network analysis, facilitates vaccine antigen discovery and predictive pre-clinical assessment of candidate vaccine antigens prior to clinical trials in humans.
Population receptive fields in the human ventral stream and their role in face perception
Lecture
Tuesday, July 12, 2016
Hour: 12:30
Location:
Gerhard M.J. Schmidt Lecture Hall
Population receptive fields in the human ventral stream and their role in face perception
Prof. Kalanit Grill-Spector
Dept of Psychology and Stanford Neurosciences Institute
Stanford University, CA
The cortical system for processing faces is a model system for studying the functional neuroanatomy of ventral temporal cortex and its role in perception for two reasons. First, the functional organization of the cortical face system is well understood. Second, activations in ventral face-selective regions are causally related to face perception. Here, I will describe recent results from our research elucidating the computations performed by population receptive field (pRFs) in the cortical system for face perception. In contrast to predictions of classical theories, recent data from my lab reveals that computations in face-selective regions in human ventral temporal cortex can be characterized with a computational pRF model, which predicts the location and spatial extent of the visual field that is processed by the neural population in a voxel. Our research characterizes pRF properties of ventral face-selective regions revealing three main findings. First, pRFs illustrate a hierarchical organization within the face system, whereby pRFs become larger and more foveal across the ventral hierarchy. Second, attention to faces modulates pRFs in face-selective regions, consequently enhancing the representation of faces in the peripheral visual field where visual acuity is the lowest. Third, our research shows that pRF properties in face-selective regions are behaviorally relevant. We find that face perception abilities are correlated with pRF properties: participants with larger pRFs perform better in face recognition than participants with smaller pRFs. These data suggest that computations performed by pRFs in face-selective regions may form a neural basis for holistic processing necessary for face recognition. Overall, these data highlight the importance of elucidating computational properties of neural populations in ventral temporal cortex as they offer a new mechanistic understanding of high-level visual processes such as face perception.
Essential Functions of Chromatin Modifications in Prefrontal Synaptic Plasticity and Working Memory
Lecture
Tuesday, June 28, 2016
Hour: 14:00
Location:
Nella and Leon Benoziyo Building for Brain Research
Essential Functions of Chromatin Modifications in Prefrontal Synaptic Plasticity and Working Memory
Mira Jakovcevski, PhD
Max Planck Institute of Psychiatry, Munich
Using Intersubject Correlation (ISC) of Dance to Study Biological Motion Processing in Autism
Lecture
Monday, June 27, 2016
Hour: 14:30
Location:
Arthur and Rochelle Belfer Building for Biomedical Research
Using Intersubject Correlation (ISC) of Dance to Study Biological Motion Processing in Autism
Prof. Frank Pollick,School of Psychology,Scotland,University of Glasgow
Several recent papers have used the technique of Intersubject Correlation (ISC) of fMRI data to study differences between typical individuals and those on the autism spectrum when they watch movies while being scanned (Byrge, et al., 2015; Salmi et al., 2013; Hasson et al., 2009). In this presentation I discuss preliminary results from a study using ISC of solo dances that explored the differences in biological motion processing in autism noted previously by our lab (McKay, et al., 2012). This will include introductory discussion of ISC studies of dance that have highlighted the possible confounding effect of using edited videos composed of different camera views (Herbec et al., 2015) as well as the motion signal that appears related to regions of highest ISC (Noble et al., 2014; Jola et al., 2013).
Encoding of spatial and temporal properties of motor tics
Lecture
Tuesday, June 21, 2016
Hour: 12:30
Location:
Gerhard M.J. Schmidt Lecture Hall
Encoding of spatial and temporal properties of motor tics
Prof. Izhar Bar-Gad
Gonda Brain Research Center,
Bar Ilan University
Striatal disinhibition leads to spontaneous abnormal action release manifesting as motor tics, resembling those expressed in Tourette syndrome patients. We utilized microstimulation within the motor cortex of freely-behaving rats before and after striatal disinhibition to study the spatial and temporal properties of tic expression. The spatial properties of these tics were dependent on the striatal organization while the temporal properties were dependent on the cortico-striatal activity. A data-driven computational model of cortico-striatal function closely replicated the temporal properties of abnormal action release. These converging experimental and computational findings suggest a clear functional dichotomy within the cortico-striatal network, pointing to disparate temporal (cortical) vs. spatial (striatal) encoding of action release.
The first steps in vision: cell types, circuits and repair
Lecture
Monday, June 13, 2016
Hour: 12:45
Location:
Gerhard M.J. Schmidt Lecture Hall
The first steps in vision: cell types, circuits and repair
Prof. Botond Roska
Friedrich Miescher Institute for Biomedical Research, Basel
Tactile discrimination with non-whisking whiskers
Lecture
Thursday, June 9, 2016
Hour: 11:00
Location:
Nella and Leon Benoziyo Building for Brain Research
Tactile discrimination with non-whisking whiskers
Prof. Daniel Shulz
CNRS, Gif sur Yvette, France
Plasticity in Tuft Dendrites of Layer 5 pyramidal neurons
Lecture
Tuesday, June 7, 2016
Hour: 12:30
Location:
Gerhard M.J. Schmidt Lecture Hall
Plasticity in Tuft Dendrites of Layer 5 pyramidal neurons
Prof. Jackie Schiller
Rappaport Faculty of Medicine, Technion, Haifa
Nonlinear decoding of a complex movie from the mammalian retina
Lecture
Thursday, June 2, 2016
Hour: 12:30
Location:
Gerhard M.J. Schmidt Lecture Hall
Nonlinear decoding of a complex movie from the mammalian retina
Prof. Gasper Tkacik
Institute of Science and Technology IST Austria
Sexually dimorphic neuronal connectivity established by sex-specific synapse pruning in C. elegans
Lecture
Wednesday, June 1, 2016
Hour: 15:00
Location:
Gerhard M.J. Schmidt Lecture Hall
Sexually dimorphic neuronal connectivity established by sex-specific synapse pruning in C. elegans
Dr. Meital Oren-Suissa
Dept of Biochemistry and Molecular Biophysics, Columbia University New York, NY
Sexually reproducing animals display sex-specific behaviors wired onto dimorphic connectivity patterns in the nervous system. The mechanisms underlying the development of sexually dimorphic nervous systems that consists mainly of shared neuronal types remain largely unknown. Within the nervous system, males and females display a number of anatomical sexual dimorphisms often in the form of neurons that are present exclusively in one, but not the other sex. In this talk I will focus on sex-specific wiring of neurons that are present in both sexes, and demonstrate the sex-specific functions of sex-shared neurons in C. elegans. The key finding that I will present is that sex-specific wiring patterns are the result of sex-specific synaptic pruning events. I will show that many neurons initially form synapses in a non-discriminatory manner in both the male and hermaphrodite pattern before sexual maturation, but sex-specific pruning events result in the sex-specific maintenance of subsets of the connections. I will describe the behavioral tests taken to show that rewiring is indicative of repurposing of the function of sensory and interneuron. I will present the conserved genes I uncovered that function to determine sex-specific connectivity patterns. To summarize I will discuss how the sexual identity of individual neurons, by initiating selective synapse loss, refines the circuitry and defines sex-specific synaptic targets. This allows for diversification of behavioral outputs with a limited set of shared neurons.
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The first steps in vision: cell types, circuits and repair
Lecture
Monday, June 13, 2016
Hour: 12:45
Location:
Gerhard M.J. Schmidt Lecture Hall
The first steps in vision: cell types, circuits and repair
Prof. Botond Roska
Friedrich Miescher Institute for Biomedical Research, Basel
Tactile discrimination with non-whisking whiskers
Lecture
Thursday, June 9, 2016
Hour: 11:00
Location:
Nella and Leon Benoziyo Building for Brain Research
Tactile discrimination with non-whisking whiskers
Prof. Daniel Shulz
CNRS, Gif sur Yvette, France
Plasticity in Tuft Dendrites of Layer 5 pyramidal neurons
Lecture
Tuesday, June 7, 2016
Hour: 12:30
Location:
Gerhard M.J. Schmidt Lecture Hall
Plasticity in Tuft Dendrites of Layer 5 pyramidal neurons
Prof. Jackie Schiller
Rappaport Faculty of Medicine, Technion, Haifa
Nonlinear decoding of a complex movie from the mammalian retina
Lecture
Thursday, June 2, 2016
Hour: 12:30
Location:
Gerhard M.J. Schmidt Lecture Hall
Nonlinear decoding of a complex movie from the mammalian retina
Prof. Gasper Tkacik
Institute of Science and Technology IST Austria
Sexually dimorphic neuronal connectivity established by sex-specific synapse pruning in C. elegans
Lecture
Wednesday, June 1, 2016
Hour: 15:00
Location:
Gerhard M.J. Schmidt Lecture Hall
Sexually dimorphic neuronal connectivity established by sex-specific synapse pruning in C. elegans
Dr. Meital Oren-Suissa
Dept of Biochemistry and Molecular Biophysics, Columbia University New York, NY
Sexually reproducing animals display sex-specific behaviors wired onto dimorphic connectivity patterns in the nervous system. The mechanisms underlying the development of sexually dimorphic nervous systems that consists mainly of shared neuronal types remain largely unknown. Within the nervous system, males and females display a number of anatomical sexual dimorphisms often in the form of neurons that are present exclusively in one, but not the other sex. In this talk I will focus on sex-specific wiring of neurons that are present in both sexes, and demonstrate the sex-specific functions of sex-shared neurons in C. elegans. The key finding that I will present is that sex-specific wiring patterns are the result of sex-specific synaptic pruning events. I will show that many neurons initially form synapses in a non-discriminatory manner in both the male and hermaphrodite pattern before sexual maturation, but sex-specific pruning events result in the sex-specific maintenance of subsets of the connections. I will describe the behavioral tests taken to show that rewiring is indicative of repurposing of the function of sensory and interneuron. I will present the conserved genes I uncovered that function to determine sex-specific connectivity patterns. To summarize I will discuss how the sexual identity of individual neurons, by initiating selective synapse loss, refines the circuitry and defines sex-specific synaptic targets. This allows for diversification of behavioral outputs with a limited set of shared neurons.
Developing behavioral flexibility
Lecture
Wednesday, June 1, 2016
Hour: 12:30
Location:
Gerhard M.J. Schmidt Lecture Hall
Developing behavioral flexibility
Prof. Catherine Hartley
Weill Cornell Medical College
Cornell University NY
Learning lays the foundation for motivated behavior, enabling us to recognize and respond appropriately to salient events. However, to function adaptively in a dynamic environment, we must be able to flexibly alter learned behavioral responses in accordance with our ongoing experience. In this talk, I will present studies examining at the cognitive, neural, and computational levels how the learning processes that support adaptive behavioral flexibility change over the course of development from childhood to adulthood. I will show that development confers marked changes in the cognitive representations engaged during learning and I will propose that learning about the degree of instrumental agency afforded by the environment may be a critical factor that shapes an individual’s behavioral repertoire.
Encoding of spatial and temporal properties of motor tics
Lecture
Tuesday, May 31, 2016
Hour: 12:30
Location:
Gerhard M.J. Schmidt Lecture Hall
Encoding of spatial and temporal properties of motor tics
Prof. Izhar Bar-Gad
Gonda Brain Research Center, Bar Ilan University
Striatal disinhibition leads to spontaneous abnormal action release manifesting as motor tics, resembling those expressed in Tourette syndrome patients. We utilized microstimulation within the motor cortex of freely-behaving rats before and after striatal disinhibition to study the spatial and temporal properties of tic expression. The spatial properties of these tics were dependent on the striatal organization while the temporal properties were dependent on the cortico-striatal activity. A data-driven computational model of cortico-striatal function closely replicated the temporal properties of abnormal action release. These converging experimental and computational findings suggest a clear functional dichotomy within the cortico-striatal network, pointing to disparate temporal (cortical) vs. spatial (striatal) encoding of action release.
Multi-level scalable proteomic interrogation of intact biological systems
Lecture
Monday, May 30, 2016
Hour: 10:00
Location:
Arthur and Rochelle Belfer Building for Biomedical Research
Multi-level scalable proteomic interrogation of intact biological systems
Prof. Kwanghun Chung
Department of Chemical Engineering Institute for Medical Engineering and Science (IMES)Picower Institute for Learning and Memory Massachusetts Institute of Technology
http://www.chunglab.org/
Unraveling unconventional role for astroglial connexins in synaptic strength and memory
Lecture
Sunday, May 29, 2016
Hour: 15:00
Location:
Gerhard M.J. Schmidt Lecture Hall
Unraveling unconventional role for astroglial connexins in synaptic strength and memory
Prof. Nathalie Rouach
CIRB, College de France, Paris
Astrocytes play active roles in brain physiology by dynamic interactions with neurons. Connexin 30, one of the two main astroglial gap-junction subunits, is thought to be involved in behavioral and basic cognitive processes. However, the underlying cellular and molecular mechanisms were unknown. We will show here in mice that connexin 30 controls hippocampal excitatory synaptic transmission through modulation of astroglial glutamate transport, which directly alters synaptic glutamate levels. Unexpectedly, we found that connexin 30 regulated cell adhesion and migration and that connexin 30 modulation of glutamate transport, occurring independently of its channel function, was mediated by morphological changes controlling insertion of astroglial processes into synaptic clefts. By setting excitatory synaptic strength, connexin 30 plays an important role in long-term synaptic plasticity and in hippocampus-based contextual memory. Taken together, these results establish connexin 30 as a critical regulator of synaptic strength by controlling the synaptic location of astroglial processes.
Experience-induced transcriptional networks that regulate the function of cortical circuits
Lecture
Tuesday, May 24, 2016
Hour: 12:30
Location:
Gerhard M.J. Schmidt Lecture Hall
Experience-induced transcriptional networks that regulate the function of cortical circuits
Dr. Ivo Spiegel
Department of Neurobiology, WIS
Inhibitory neurons are critically important for the adaptation of neural circuits to sensory experience, but the molecular mechanisms by which experience controls the connectivity between different types of inhibitory neurons to regulate cortical plasticity are largely unknown. In this talk, I will present studies demonstrating that sensory experience induces in cortical vasoactive intestinal peptide (VIP)-expressing neurons a gene program that is markedly distinct from that induced in excitatory neurons and other subtypes of inhibitory neuron. I will show that is Igf1 one of several activity-regulated genes that are specific to VIP neurons, that IGF1 functions cell-autonomously in VIP neurons to increase inhibitory synaptic input onto these neurons and that VIP neuron-derived IGF1 regulates visual acuity in an experience-dependent manner, likely by promoting the inhibition of disinhibitory neurons and affecting inhibition onto cortical pyramidal neurons. I will discuss how our findings support a model by which experience-induced transcriptional networks regulate the synaptic connectivity of each type of neuron according to a circuit-wide homeostatic logic and I will propose that the analysis of the genomic mechanisms regulating these transcriptional networks will allow us to evaluate the extent to which cell-type-specific homeostatic mechanisms contribute to the function of cortical circuits.
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