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1.
J Comp Neurol ; 528(7): 1113-1139, 2020 05.
Article in English | MEDLINE | ID: mdl-31710697

ABSTRACT

Calcium (Ca2+ ) dysregulation has been linked to neuronal cell death, including in hereditary retinal degeneration. Ca2+ dysregulation is thought to cause rod and cone photoreceptor cell death. Spatial and temporal heterogeneities in retinal disease models have hampered validation of this hypothesis. We examined the role of Ca2+ in photoreceptor degeneration, assessing the activation pattern of Ca2+ -dependent calpain proteases, generating spatiotemporal maps of the entire retina in the cpfl1 mouse model for primary cone degeneration, and in the rd1 and rd10 models for primary rod degeneration. We used Gaussian process models to distinguish the temporal sequences of degenerative molecular processes from other variability sources.In the rd1 and rd10 models, spatiotemporal pattern of increased calpain activity matched the progression of primary rod degeneration. High calpain activity coincided with activation of the calpain-2 isoform but not with calpain-1, suggesting differential roles for both calpain isoforms. Primary rod loss was linked to upregulation of apoptosis-inducing factor, although only a minute fraction of cells showed activity of the apoptotic marker caspase-3. After primary rod degeneration concluded, caspase-3 activation appeared in cones, suggesting apoptosis as the dominant mechanism for secondary cone loss. Gaussian process models highlighted calpain activity as a key event during primary rod photoreceptor cell death. Our data suggest a causal link between Ca2+ dysregulation and primary, nonapoptotic degeneration of photoreceptors and a role for apoptosis in secondary degeneration of cones, highlighting the importance of the spatial and temporal location of key molecular events, which may guide the evaluation of new therapies.


Subject(s)
Calpain/metabolism , Retinal Degeneration/metabolism , Retinal Degeneration/pathology , Animals , Calcium/metabolism , Cell Death/physiology , Disease Models, Animal , Mice , Mice, Inbred C57BL , Mice, Mutant Strains , Retinal Cone Photoreceptor Cells/metabolism , Retinal Cone Photoreceptor Cells/pathology , Retinal Rod Photoreceptor Cells/metabolism , Retinal Rod Photoreceptor Cells/pathology
2.
PLoS Comput Biol ; 15(10): e1007473, 2019 Oct.
Article in English | MEDLINE | ID: mdl-31639125

ABSTRACT

[This corrects the article DOI: 10.1371/journal.pcbi.1007205.].

3.
PLoS Comput Biol ; 15(8): e1007205, 2019 08.
Article in English | MEDLINE | ID: mdl-31374071

ABSTRACT

Variability, stochastic or otherwise, is a central feature of neural activity. Yet the means by which estimates of variation and uncertainty are derived from noisy observations of neural activity is often heuristic, with more weight given to numerical convenience than statistical rigour. For two-photon imaging data, composed of fundamentally probabilistic streams of photon detections, the problem is particularly acute. Here, we present a statistical pipeline for the inference and analysis of neural activity using Gaussian Process regression, applied to two-photon recordings of light-driven activity in ex vivo mouse retina. We demonstrate the flexibility and extensibility of these models, considering cases with non-stationary statistics, driven by complex parametric stimuli, in signal discrimination, hierarchical clustering and other inference tasks. Sparse approximation methods allow these models to be fitted rapidly, permitting them to actively guide the design of light stimulation in the midst of ongoing two-photon experiments.


Subject(s)
Bayes Theorem , Microscopy, Fluorescence, Multiphoton/statistics & numerical data , Models, Neurological , Animals , Calcium Signaling , Computational Biology , Glutamic Acid/physiology , Heuristics , In Vitro Techniques , Mice , Mice, Inbred C57BL , Mice, Transgenic , Models, Statistical , Neurons/physiology , Normal Distribution , Photic Stimulation , Regression Analysis , Retina/physiology , Retina/radiation effects , Signal-To-Noise Ratio , Uncertainty
4.
PLoS Comput Biol ; 14(5): e1006157, 2018 05.
Article in English | MEDLINE | ID: mdl-29782491

ABSTRACT

In recent years, two-photon calcium imaging has become a standard tool to probe the function of neural circuits and to study computations in neuronal populations. However, the acquired signal is only an indirect measurement of neural activity due to the comparatively slow dynamics of fluorescent calcium indicators. Different algorithms for estimating spike rates from noisy calcium measurements have been proposed in the past, but it is an open question how far performance can be improved. Here, we report the results of the spikefinder challenge, launched to catalyze the development of new spike rate inference algorithms through crowd-sourcing. We present ten of the submitted algorithms which show improved performance compared to previously evaluated methods. Interestingly, the top-performing algorithms are based on a wide range of principles from deep neural networks to generative models, yet provide highly correlated estimates of the neural activity. The competition shows that benchmark challenges can drive algorithmic developments in neuroscience.


Subject(s)
Action Potentials/physiology , Calcium/metabolism , Computational Biology/methods , Models, Neurological , Algorithms , Animals , Calcium/chemistry , Calcium/physiology , Databases, Factual , Mice , Molecular Imaging , Optical Imaging , Retina/cytology , Retinal Neurons/cytology , Retinal Neurons/metabolism
5.
Curr Biol ; 27(23): 3603-3615.e5, 2017 Dec 04.
Article in English | MEDLINE | ID: mdl-29174891

ABSTRACT

The mouse retina contains a single type of horizontal cell, a GABAergic interneuron that samples from all cone photoreceptors within reach and modulates their glutamatergic output via parallel feedback mechanisms. Because horizontal cells form an electrically coupled network, they have been implicated in global signal processing, such as large-scale contrast enhancement. Recently, it has been proposed that horizontal cells can also act locally at the level of individual cone photoreceptors. To test this possibility physiologically, we used two-photon microscopy to record light stimulus-evoked Ca2+ signals in cone axon terminals and horizontal cell dendrites as well as glutamate release in the outer plexiform layer. By selectively stimulating the two mouse cone opsins with green and UV light, we assessed whether signals from individual cones remain isolated within horizontal cell dendritic tips or whether they spread across the dendritic arbor. Consistent with the mouse's opsin expression gradient, we found that the Ca2+ signals recorded from dendrites of dorsal horizontal cells were dominated by M-opsin and those of ventral horizontal cells by S-opsin activation. The signals measured in neighboring horizontal cell dendritic tips varied markedly in their chromatic preference, arguing against global processing. Rather, our experimental data and results from biophysically realistic modeling support the idea that horizontal cells can process cone input locally, extending the classical view of horizontal cell function. Pharmacologically removing horizontal cells from the circuitry reduced the sensitivity of the cone signal to low frequencies, suggesting that local horizontal cell feedback shapes the temporal properties of cone output.


Subject(s)
Axons/physiology , Dendrites/physiology , Mice/physiology , Retinal Cone Photoreceptor Cells/physiology , Signal Transduction , Animals , Calcium/metabolism , Female , Glutamic Acid/metabolism , Male , Mice, Transgenic , Microscopy, Fluorescence, Multiphoton , Retinal Cone Photoreceptor Cells/cytology
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