Recipient organisationCardiff UniversitySource-published name: Cardiff University
Funding£1.5M
PeriodJan 2022 — Jan 2027
In plain English
AI plain-English summary
A mouse’s whiskers are helping scientists watch how the brain’s learning circuits physically rewire during a simple texture-discrimination task. The cerebral cortex stores long-term memories, but how it organises learning across its many specialised regions remains unknown. This programme focuses on a recurring circuit module—pyramidal neurons in layers 2 and 3 that receive both sensory input and feedback from higher brain areas. The team will test whether feedback connections act as a gate, allowing or blocking synaptic plasticity on the sensory inputs, and whether a specific class of inhibitory neurons controls that gate. If the hypothesis holds, the work would reveal a fundamental mechanism for how the cortex encodes learned associations. Because a mutation linked to schizophrenia (DISC1) disrupts the normal separation of inputs on these neurons, the research could also explain how mis-wiring in this circuit contributes to cognitive deficits in mental health conditions. This is primarily fundamental science, but understanding a core memory substrate could eventually inform strategies for treating learning and memory disorders.
View original technical description
One of the great challenges in Neuroscience is understanding how learning and memory work. Long term memory is thought to be stored in the cerebral cortex. The cerebral cortex is particularly highly developed in humans. It is involved in almost every aspect of behaviour and cognition from sensory processing and planning for action, through to logical reasoning and imaginative thought. How therefore is learning and memory organised in such a diverse structure? Our aim in this programme of work is to understand a component of the cortical circuit that forms a recurring module throughout most cortical areas and may provide a common substrate for learning and long-term memory across the great variety of modalities that compose the cortical repertoire. We will study pyramidal neurones that receive both feedback connections from higher order cortical areas and ascending feedforward connections carrying sensory information. While feedback connections target apical dendrites, the feedforward connections favour the basal dendrites of the pyramidal cells. The pyramidal neurones in question are located in layers 2 and 3 (L2/3). We will study them in a relatively simple yet highly organised part of the mouse cerebral cortex (known as the barrel cortex) that receives tactile information from the whiskers. We will observe how feedback information from higher order cortical areas interacts with L2/3 neurones when the animal learns a tactile texture discrimination task, for example distinguishes between rough and smooth surfaces. We will test the hypothesis that feedback connections gate synaptic plasticity on the feedforward connections and thereby encode features of the stimulus advantageous for learning the discrimination. Furthermore, we will test the idea that a subset of inhibitory interneurones that target the apical dendrites are able to control the interaction between the feedback and feedforward connections and thereby exert control over synaptic plasticity. The programme of work comprises experiments where 1. we probe the nature and operation of the cortical circuit in some detail using in vitro brain slices and measure the plasticity by observing a synaptic process known as long-term potentiation (LTP) and 2. we test how the components of the circuit behave in whole animals (in vivo) when they learn to distinguish between two tactile textures in a discrimination task to gain a reward 3. we measure structural plasticity in the L2/3 cells during learning with and without the correct feedback. Preliminary studies show that our texture discrimination task depends on barrel cortex, can be learned by mice over a few days and causes structural plasticity in the L2/3 neurones. The feedback connections from higher order cortical areas can be made to express artificial ion channels that can be activated by light (optogenetics), allowing us to selectively stimulate feedback connections 1. in cortical slices to gate LTP in vitro or 2. during tactile learning in vivo to bias choices toward one texture or the other. Our studies probe what we believe is a fundamental component of the long-term memory system. Its correct operation relies on the separation of connections on apical and basal dendrites. However, in a mutation that is known to cause mental health conditions in people (DISC1 t(1;11)), we have found that the balance between apical and basal dendrites of pyramidal cells is altered (in barrel cortex and prefrontal cortex). Connections normally directed to basal dendrites are found to excite apical dendrites, due to developmental atrophy of the basal dendrites. To understand the extent of this mis-wiring and its consequences for plasticity we will map excitatory and inhibitory inputs in the mutants using optogenetics methods and determine the ability of inhibition to control apical gating of plasticity. This aspect of the study could help explain how cognitive deficits arise in mental health conditions like schizophrenia.
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