Topic: Hebbian learning

Even in stable environments, sensory responses undergo continuous reformatting, a phenomenon known as representational drift. Using chronic calcium imaging in mouse auditory cortex, we show that during this representational drift signal correlations predict future noise correlations, suggesting that stimulus-driven co-activation strengthens effective connectivity via Hebbian-like plasticity. Linear network models reveal that these temporal dependencies between signal and noise correlations emerge only when Hebbian learning balances stochastic synaptic changes, preventing functional degradation

Cognitive maps confer animals with flexible intelligence by representing spatial, temporal, and abstract relationships that can be used to shape thought, planning, and behavior. Cognitive maps have been observed in the hippocampus, but their algorithmic form and the processes by which they are learned remain obscure. Here, we employed large-scale, longitudinal two-photon calcium imaging to record activity from thousands of neurons in the CA1 region of the hippocampus while mice learned to efficiently collect rewards from two subtly different versions of linear tracks in virtual reality. The r

Brains often infer low-dimensional features from high-dimensional input. For example, during visual processing a picture captured by the retina is processed hierarchically through the ventral stream, which gradually infers higher-level features encoded by the lower number of neurons. However, it is still unclear how neural networks learn to perform such tasks. Hebbian Learning (HL), a local form of plasticity that uses pre- and postsynaptic activity to change synaptic efficacy, has been used extensively in receptive field models, sparse coding, independent and principal component analysis, an

Understanding the neural code for vision remains a major challenge for neuroscience, with recent efforts influenced by the success of convolutional neural networks. However, spiking neurons make biological vision fundamentally different from the firing rate model implicit in these artificial neural networks. In region V1 of the primate visual cortex, a flashed image is processed in tens of milliseconds, allowing time for only a few action potentials, typically across a small subset of neurons. Moreover, persistent eye motion (ocular drift) changes the location of retinal responses, and thus

The successor representation (SR) is a promising candidate principle for hippocampal function. Theory proposes that each place cell encodes the expected state occupancy of its target location in the near future. This framework has desirable consequences on the generalisability and efficiency of reinforcement learning algorithms operating over these representations and is supported by behavioural and electrophysiological evidence. However, it is unclear how the SR might be learnt in the brain. Temporal difference learning, commonly used to learn SRs in artificial agents, is not known to be impl

Despite the recent success of deep learning in artificial intelligence, the lack of biological plausibility and labeled data in natural learning still poses a challenge in understanding biological learning. At the other extreme lies Hebbian learning, the simplest local and unsupervised one, yet considered to be computationally less efficient. In this talk, I would introduce a novel method to infer the form of Hebbian learning from in vivo data. Applying the method to the data obtained from the monkey inferior temporal cortex for the recognition task indicates how Hebbian learning changes th

Humans and other primates exhibit rich and versatile behaviour, switching nimbly between tasks as the environmental context requires. I will discuss the neural coding patterns that make this possible in humans and deep networks. First, using deep network simulations, I will characterise two distinct solutions to task acquisition (“lazy” and “rich” learning) which trade off learning speed for robustness, and depend on the initial weights scale and network sparsity. I will chart the predictions of these two schemes for a context-dependent decision-making task, showing that the rich solution is

Spiking neural networks (SNNs) are characterized by low power consumption, highly parallel computation and event-driven information processing [1]. Many of the concepts that promise to improve the efficiency of SNNs compared to conventional deep neural networks, such as spikes, sparsity, and static suppression, are inspired by our understanding of how the brain processes information. Hence, we can further advance the development of SNNs by improving our current knowledge of how biological neural networks learn through spike-based local plasticity mechanisms. In recent years, many spike-based

Learning in neuronal circuits requires coordinated modifications of synaptic strengths across hierarchical networks to refine computation and improve behavioral outcomes. This coordination requires solving the credit assignment problem. Yet, how neuronal circuits achieve credit assignment remains a central unsolved question in systems neuroscience [1]. Several modeling studies have suggested putative biological mechanisms for back-propagating error signals through multi-layer networks. These functionally motivated models assume distinct neuronal compartments representing local error signals t

To successfully inform behavior, cortical circuits must produce consistent patterns of neuronal activity within and across trials that allow for reliable stimulus discrimination. Under this perspective, any response variability appears detrimental to sensory systems as it severely limits stimulus discriminability. Here, we propose a beneficial role of response variability: to facilitate faster learning in feedforward-recurrent networks through a self-stabilizing feedback mechanism. We explore this hypothesis in the framework of learning novel stimulus representations in pre-structured recurren