Biology subjects

Josić, K.

Publications and source records attributed to Josić, K..

3 recordsLinked to original sources

bioRxiv2017

From the statistics of connectivity to the statistics of spike times in neuronal networks

An essential step toward understanding neural circuits is linking their structure and their dynamics. In general, this relationship can be almost arbitrarily complex. Recent theoretical work has, however, begun to identify some broad principles underlying collective spiking activity in neural circuits. The first is that local features of network connectivity can be surprisingly effective in predicting global statistics of activity across a network. The second is that, for the important case of large networks with excitatory-inhibitory balance, correlated spiking persists or vanishes depending on the spatial scales of recurrent and feedforward connectivity. We close by showing how these ideas, together with plasticity rules, can help to close the loop between network structure and activity statistics.\n\nHighlightsO_LIRemarkable new data on connectivity and activity raise the promise and raise the bar for linking structure and dynamics in neural networks.\nC_LIO_LIRecent theories aim at a statistical approach, in which the enormous complexity of wiring diagrams is reduced to key features of that connectivity that drive coherent, network-wide activity.\nC_LIO_LIWe provide a unified view of three branches of this work, tied to a broadly useful \"neural response\" formula that explicitly relates connectivity to spike train statistics.\nC_LIO_LIThis isolates a surprisingly systematic role for the local structure and spatial scale of connectivity in determining spike correlations, and shows how the coevolution of structured connectivity and spiking statistics through synaptic plasticity can be predicted self-consistently.\nC_LI

neuroscience↗

bioRxiv2017

Modeling mechanical interactions in growing populations of rod-shaped bacteria

Advances in synthetic biology allow us to engineer bacterial collectives with pre-specified characteristics. However, the behavior of these collectives is difficult to understand, as cellular growth and division as well as extra-cellular fluid flow lead to complex, changing arrangements of cells within the population. To rationally engineer and control the behavior of cell collectives we need theoretical and computational tools to understand their emergent spatiotemporal dynamics. Here, we present an agent-based model that allows growing cells to detect and respond to mechanical interactions. Crucially, our model couples the dynamics of cell growth to the cells environment: Mechanical constraints can affect cellular growth rate and a cell may alter its behavior in response to these constraints. This coupling links the mechanical forces that influence cell growth and emergent behaviors in cell assemblies. We illustrate our approach by showing how mechanical interactions can impact the dynamics of bacterial collectives growing in microfluidic traps.

synthetic biology↗

bioRxiv2016

Linking structure and activity in nonlinear spiking networks

Recent experimental advances are producing an avalanche of data on both neural connectivity and neural activity. To take full advantage of these two emerging datasets we need a framework that links them, revealing how collective neural activity arises from the structure of neural connectivity and intrinsic neural dynamics. This problem of structure-driven activity has drawn major interest in computational neuroscience. Existing methods for relating activity and architecture in spiking networks rely on linearizing activity around a central operating point and thus fail to capture the nonlinear responses of individual neurons that are the hallmark of neural information processing. Here, we overcome this limitation and present a new relationship between connectivity and activity in networks of nonlinear spiking neurons by developing a diagrammatic fluctuation expansion based on statistical field theory. We explicitly show how recurrent network structure produces pairwise and higher-order correlated activity, and how nonlinearities impact the networks' spiking activity. Our findings open new avenues to investigating how single-neuron nonlinearities--including those of different cell types--combine with connectivity to shape population activity and function.

neuroscience↗