105 research outputs found
Mapping the spatiotemporal dynamics of calcium signaling in cellular neural networks using optical flow
An optical flow gradient algorithm was applied to spontaneously forming net-
works of neurons and glia in culture imaged by fluorescence optical microscopy
in order to map functional calcium signaling with single pixel resolution.
Optical flow estimates the direction and speed of motion of objects in an image
between subsequent frames in a recorded digital sequence of images (i.e. a
movie). Computed vector field outputs by the algorithm were able to track the
spatiotemporal dynamics of calcium signaling pat- terns. We begin by briefly
reviewing the mathematics of the optical flow algorithm, and then describe how
to solve for the displacement vectors and how to measure their reliability. We
then compare computed flow vectors with manually estimated vectors for the
progression of a calcium signal recorded from representative astrocyte
cultures. Finally, we applied the algorithm to preparations of primary
astrocytes and hippocampal neurons and to the rMC-1 Muller glial cell line in
order to illustrate the capability of the algorithm for capturing different
types of spatiotemporal calcium activity. We discuss the imaging requirements,
parameter selection and threshold selection for reliable measurements, and
offer perspectives on uses of the vector data.Comment: 23 pages, 5 figures. Peer reviewed accepted version in press in
Annals of Biomedical Engineerin
Signal Propagation in Feedforward Neuronal Networks with Unreliable Synapses
In this paper, we systematically investigate both the synfire propagation and
firing rate propagation in feedforward neuronal network coupled in an
all-to-all fashion. In contrast to most earlier work, where only reliable
synaptic connections are considered, we mainly examine the effects of
unreliable synapses on both types of neural activity propagation in this work.
We first study networks composed of purely excitatory neurons. Our results show
that both the successful transmission probability and excitatory synaptic
strength largely influence the propagation of these two types of neural
activities, and better tuning of these synaptic parameters makes the considered
network support stable signal propagation. It is also found that noise has
significant but different impacts on these two types of propagation. The
additive Gaussian white noise has the tendency to reduce the precision of the
synfire activity, whereas noise with appropriate intensity can enhance the
performance of firing rate propagation. Further simulations indicate that the
propagation dynamics of the considered neuronal network is not simply
determined by the average amount of received neurotransmitter for each neuron
in a time instant, but also largely influenced by the stochastic effect of
neurotransmitter release. Second, we compare our results with those obtained in
corresponding feedforward neuronal networks connected with reliable synapses
but in a random coupling fashion. We confirm that some differences can be
observed in these two different feedforward neuronal network models. Finally,
we study the signal propagation in feedforward neuronal networks consisting of
both excitatory and inhibitory neurons, and demonstrate that inhibition also
plays an important role in signal propagation in the considered networks.Comment: 33pages, 16 figures; Journal of Computational Neuroscience
(published
Image informatics strategies for deciphering neuronal network connectivity
Brain function relies on an intricate network of highly dynamic neuronal connections that rewires dramatically under the impulse of various external cues and pathological conditions. Among the neuronal structures that show morphologi- cal plasticity are neurites, synapses, dendritic spines and even nuclei. This structural remodelling is directly connected with functional changes such as intercellular com- munication and the associated calcium-bursting behaviour. In vitro cultured neu- ronal networks are valuable models for studying these morpho-functional changes. Owing to the automation and standardisation of both image acquisition and image analysis, it has become possible to extract statistically relevant readout from such networks. Here, we focus on the current state-of-the-art in image informatics that enables quantitative microscopic interrogation of neuronal networks. We describe the major correlates of neuronal connectivity and present workflows for analysing them. Finally, we provide an outlook on the challenges that remain to be addressed, and discuss how imaging algorithms can be extended beyond in vitro imaging studies
Two-way communication with neural networks in vivo using focused light
Neuronal networks process information in a distributed, spatially heterogeneous manner that transcends the layout of electrodes. In contrast, directed and steerable light offers the potential to engage specific cells on demand. We present a unified framework for adapting microscopes to use light for simultaneous in vivo stimulation and recording of cells at fine spatiotemporal resolutions. We use straightforward optics to lock onto networks in vivo, to steer light to activate circuit elements and to simultaneously record from other cells. We then actualize this 'free' augmentation on both an 'open' two-photon microscope and a leading commercial one. By following this protocol, setup of the system takes a few days, and the result is a noninvasive interface to brain dynamics based on directed light, at a network resolution that was not previously possible and which will further improve with the rapid advance in development of optical reporters and effectors. This protocol is for physiologists who are competent with computers and wish to extend hardware and software to interface more fluidly with neuronal networks.National Institutes of Health (U.S.) (Postdoctoral Fellowship)Simons Foundation (Postdoctoral Fellowship)National Institutes of Health (U.S.) (Predoctoral Fellowship)National Institutes of Health (U.S.)Simons Foundatio
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