The computational foundations of dynamic coding in working memory.

Working memory (WM) is a fundamental aspect of cognition. WM maintenance is classically thought to rely on stable patterns of neural activities. However, recent evidence shows that neural population activities during WM maintenance undergo dynamic variations before settling into a stable pattern. Although this has been difficult to explain theoretically, neural network models optimized for WM typically also exhibit such dynamics. Here, we examine stable versus dynamic coding in neural data, classical models, and task-optimized networks. We review principled mathematical reasons for why classical models do not, while task-optimized models naturally do exhibit dynamic coding. We suggest an update to our understanding of WM maintenance, in which dynamic coding is a fundamental computational feature rather than an epiphenomenon.

Optimal information loading into working memory explains dynamic coding in the prefrontal cortex.

Working memory involves the short-term maintenance of information and is critical in many tasks. The neural circuit dynamics underlying working memory remain poorly understood, with different aspects of prefrontal cortical (PFC) responses explained by different putative mechanisms. By mathematical analysis, numerical simulations, and using recordings from monkey PFC, we investigate a critical but hitherto ignored aspect of working memory dynamics: information loading. We find that, contrary to common assumptions, optimal loading of information into working memory involves inputs that are largely orthogonal, rather than similar, to the late delay activities observed during memory maintenance, naturally leading to the widely observed phenomenon of dynamic coding in PFC. Using a theoretically principled metric, we show that PFC exhibits the hallmarks of optimal information loading. We also find that optimal information loading emerges as a general dynamical strategy in task-optimized recurrent neural networks. Our theory unifies previous, seemingly conflicting theories of memory maintenance based on attractor or purely sequential dynamics and reveals a normative principle underlying dynamic coding.

Publisher Correction: Motor primitives in space and time via targeted gain modulation in cortical networks.

In the version of this article initially published, in the PDF, equations (2) and (4) erroneously displayed a curly bracket on the right hand side of the equation. This should not be there. The errors have been corrected in the PDF version of the article. The equations appear correctly in the HTML.

Motor primitives in space and time via targeted gain modulation in cortical networks.

Motor cortex (M1) exhibits a rich repertoire of neuronal activities to support the generation of complex movements. Although recent neuronal-network models capture many qualitative aspects of M1 dynamics, they can generate only a few distinct movements. Additionally, it is unclear how M1 efficiently controls movements over a wide range of shapes and speeds. We demonstrate that modulation of neuronal input-output gains in recurrent neuronal-network models with a fixed architecture can dramatically reorganize neuronal activity and thus downstream muscle outputs. Consistent with the observation of diffuse neuromodulatory projections to M1, a relatively small number of modulatory control units provide sufficient flexibility to adjust high-dimensional network activity using a simple reward-based learning rule. Furthermore, it is possible to assemble novel movements from previously learned primitives, and one can separately change movement speed while preserving movement shape. Our results provide a new perspective on the role of modulatory systems in controlling recurrent cortical activity.

Cortical Signal Propagation: Balance, Amplify, Transmit.

The neural code of cortical processing remains uncracked; however, it must necessarily rely on faithful signal propagation between cortical areas. In this issue of Neuron, Joglekar et al. (2018) show that strong inter-areal excitation balanced by local inhibition can enable reliable signal propagation in data-constrained network models of macaque cortex.