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Biology subjects

Ritter, L.

Publications and source records attributed to Ritter, L..

2 recordsLinked to original sources

Efficient Working Memory Maintenance via High-Dimensional Rotational Dynamics

Working memory (WM) is fundamental to higher-order cognition, yet the circuit mechanisms through which memoranda are maintained in neural activity after removal of sensory input remain subject to vigorous debate. Prominent theories propose that stimuli are encoded in either stable and persistent activity patterns configured through attractor mechanisms or dynamic and time-varying activity patterns brought about through functionally-feedforward network architectures. However, cortical circuits exhibit heterogeneous responses during WM tasks that are challenging to reconcile with either hypothesis. We hypothesised that these complex response dynamics could emerge from an optimally noise-robust and energetically efficient solution to WM tasks. We show that, in contrast to previous theories, networks optimised for efficient WM encoding exhibit high-dimensional rotational dynamics. We find direct evidence for these rotational dynamics in large-scale recordings from monkey prefrontal cortex. Our findings suggest that the complex and dynamic response properties of WM circuits emerge from efficient coding principles.

neuroscience↗

Tunable bicontinuous macroporous cell culture scaffolds via kinetically controlled phase separation

Three-dimensional (3D) scaffolds enable biological investigations with a more natural cell conformation. However, the porosity of synthetic hydrogels is often limited to the nanometer scale, which confines the movement of 3D encapsulated cells and restricts dynamic cell processes. Precise control of hydrogel porosity across length scales remains a challenge and the development of porous materials that allow cell infiltration, spreading, and migration in a manner more similar to natural ECM environments is desirable. Here, we present a straightforward and reliable method for generating kinetically-controlled macroporous systems using liquid-liquid phase separation between poly(ethylene glycol) (PEG) and dextran. Photopolymerization-induced phase separation resulted in macroporous hydrogels with tunable pore size. Varying light intensity and hydrogel composition controlled polymerization kinetics, time to percolation, and complete gelation, which defined the average pore diameter (O = 1- 300 m) and final gel stiffness of the formed hydrogels. Critically, for biological applications, macroporous hydrogels were prepared from aqueous polymer solutions at physiological pH and temperature using visible light, allowing for direct cell encapsulation. We encapsulated human dermal fibroblasts in a range of macroporous gels with different pore sizes. Porosity improved cell spreading with respect to bulk gels and allowed migration in the porous systems.

bioengineering↗