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Jedlicka, P.

Publications and source records attributed to Jedlicka, P..

At least 19 recordsLinked to original sources

Dendrite Control Theory: A Unifying Framework Bridging Neuronal Morphology And Dendritic Voltage Behavior

Control theory and dendritic computation have revolutionized their respective fields, yet they rarely converge. Here, we use control theory as a framework to reveal how dendritic morphology and synaptic input organization constrain structural resilience and energy cost. Treating diverse dendritic trees as connected network nodes, we demonstrate that the degree of structural symmetry dictates easy- versus hard-to-access control states. Notably, control inputs restricted solely to peripheral terminal branches are mathematically sufficient to govern the voltage states of the entire dendrite and soma, granting striking resilience against input loss elsewhere. Conversely, limiting input dimensionality amplifies voltage fluctuations and metabolic costs. These findings expose fundamental biophysical trade-offs between wiring cost, functional flexibility, robustness, and energy efficiency, suggesting interneurons generally exhibit higher resilience while excitatory neurons feature superior controllability. We introduce 'Dendrite Control Theory' as a rigorous engineering framework linking neuronal morphology directly to computation and robustness, offering a new neuroscience research paradigm.

neuroscience↗

An energy-dependent integrate-and-fire model explains coordinated synaptic and intrinsic adaptation under metabolic stress

Neuronal computation is constrained by the energetic cost of maintaining synaptic transmission, ionic gradients and action-potential generation. Prior work has shown that food restriction in mice shifts visual cortical neurons toward a different operating regime characterized by reduced excitatory synaptic drive, increased membrane resistance and a more depolarized resting membrane potential. This preserves neuronal firing rates, but comes at the cost of reduced coding precision. Deriving an improved estimate of neuronal energy consumption, we have recently shown that these adaptations reflect an optimal trade-off between neuronal information transmission and energy consumption. However, it remains unclear through which control strategies individual neurons adapt their biophysical parameters to maintain a favorable energy-information trade-off. Here we consider several candidate models implementing different control strategies. A "synapses-first" model, in which metabolic stress drives a downscaling of synaptic efficacies to save energy, while an intrinsic plasticity mechanism increases excitability to preserve the average firing rate, successfully reproduces key experimental observations. Alternative models in which energy shortages drive changes in intrinsic excitability or firing-rate variability can also reproduce the endpoint of neuronal adaptation, but predict different time courses and exhibit less energy-efficient and less stable dynamics. New experiments are needed to distinguish among these competing models.

neuroscience↗

Hippocampal granule cells balance energy and function along the Pareto optimal front

The dentate gyrus' principal neuron, the granule cell (GC), plays a key role in pattern separation, transforming similar inputs into dissimilar outputs. We used a new measure based on information theory to evaluate this transformation in an experimentally derived in silico GC model with realistic ion channel distributions across its dendrites. We found that model performance aligned well with current-clamp recordings from mouse brain slices. However, it was also possible to find artificial parameter combinations in the model that functionally outperformed the recorded cells while matching their action potential shapes. Rather than maximising computational power, the biologically realistic GC model balanced energy efficiency against increased functionality in a Pareto optimal way: No possible parameter combination was found to improve one of the objectives without impairing the other. Interestingly, immature GCs adopted a different weighted trade-off with a stronger emphasis on energy efficiency than pattern separation, but they remained Pareto optimal over their putative developmental trajectory. Our results support the idea that evolution favours neurons that can satisfy functional and energetic demands simultaneously.

neuroscience↗

Nowhere to Hide: The Effect of Centromere Architecture on LTR Retrotransposon Dynamics

Centromere architecture can determine where transposable elements persist, yet its effects on retrotransposon turnover remain poorly understood. Here we test a chromosome-level "nowhere-to-hide" model, in which holocentric chromosomes, owing to distributed centromere activity and reduced chromatin compartmentalization, provide fewer stable repeat-rich refugia than monocentric chromosomes. We combined genome-wide LTR retrotransposon annotation, spatial modelling and FISH across 40 holocentric plant species and 31 closely related monocentric relatives from Poales, Cuscuta, and Melanthiaceae. Overall LTR retrotransposon abundance and Ty1-copia/Ty3-gypsy composition were explained mainly by lineage history and chromosome size, rather than by holocentricity itself. By contrast, element persistence and removal showed dependence on centromere architecture. Intact LTR retrotransposons were younger in holocentric genomes, and holocentric chromosomes lacked the chromosome-size-dependent spatial clustering of element age observed in monocentrics. Solo-LTR profiles further revealed weaker spatial clustering of removal signatures in holocentric chromosomes, consistent with a more homogeneous chromosome-wide landscape of ectopic recombination. Epigenomic analyses of a matched Luzula-Juncus pair indicated that young elements can occur in centromeric chromatin, whereas solo LTRs are associated with more euchromatic contexts. These results support the nowhere-to-hide model, showing that centromere architecture does not shape LTR retrotransposons accumulation, but their persistence and removal efficiency.

evolutionary biology↗

Morphological differences along the radial gradient of hippocampal area CA2 pyramidal neuron dendrites

Hippocampal area CA2 has recently emerged as a critical region for social recognition memory. Furthermore, this understudied region has been implicated in psychiatric diseases and neurodegenerative diseases. There has been accumulating evidence indicating that the pyramidal neurons (PNs) in area CA2 exhibit functional specializations that correlate with somatic position in stratum pyramidale (sp). In this study, we investigated the morphological differences in dendritic architecture of CA2 PNs with a focus on the radial gradient, i.e., along the deep-superficial axis of the sp. We conducted a comprehensive morphological analysis including Sholl intersection profiles, branching order distributions, root angle distributions, and dendritic cable lengths. We found that CA2 PNs have fewer oblique dendrites and a larger number of tuft-like dendrites as compared to CA1 PNs. Furthermore, within the CA2 population, we found that many of the dendritic structural features gradually changed along the radial axis from deep to superficial somatic location, indicating a continuum of dendritic morphology rather than two sharply defined subtypes of pyramidal neurons. This morphological characterization may serve as a starting point to better understand the corresponding functional organization of CA2. The gradual difference between deeper and superficial CA2 PNs suggests a continuum of their computational capabilities beyond two binary functional classes. In briefUsing several methods, we examine the dendritic morphology of over 130 CA2 and CA1 pyramidal neurons and find that many properties such as the cable length and terminal numbers of the dendritic arbors vary as a with the location of the soma in the pyramidal layer. HighlightsO_LIWe use scholl analysis, graph theory and machine learning techniques to quantify the different dendritic morphologies of CA2 pyramidal neurons. C_LIO_LIMany properties of CA2 pyramidal neuron apical dendrites vary as a function of somatic location in the pyramidal layer. C_LIO_LIMore superficial CA2 pyramidal neurons have longer oblique apical dendrites, and shorter tuft dendrites. C_LI

neuroscience↗

Population collapse of the Egyptian fruit bat on Cyprus (2005-2022) was likely driven by roost disturbance and declining food availability linked to climate change

Peripheral island populations are often especially vulnerable to environmental change, yet they may also represent unique components of biodiversity. We assessed long-term population change in the Egyptian fruit bat (Rousettus aegyptiacus) on Cyprus, the only insular and geographically isolated population of this pteropodid in Europe, and evaluated two non-exclusive explanations for its decline: roost disturbance and reduced food availability. We analysed roost counts from 21 underground sites monitored between 2005 and 2022 and modelled temporal trends in commercially produced fruits used by the species. The monitored population declined from c. 7200 to c. 1050 individuals, corresponding to an estimated decrease of 85.4%. The decline was steepest during 2005-2011, slowed during 2012-2017, and was followed by partial recovery in 2018-2022. Colonies in easily accessible roosts declined significantly faster than those in less accessible roosts, consistent with an important role of human disturbance. Fruit production showed strong long-term declines and multiple structural breaks clustered in the mid-2000s, coinciding with the most severe phase of population decline and a major drought period on Cyprus. The fate of the missing portion of the population remains uncertain. Although large-scale mortality cannot be excluded, there was no clear evidence of widespread starvation-related mortality, and emigration to nearby mainland areas remains a plausible but untested explanation. Overall, our results indicate that the collapse of this peripheral island population was most likely driven by a combination of roost disturbance and reduced food availability associated with climate-related environmental change, highlighting the urgent need for strict roost protection and measures to secure food and water resources.

ecology↗

Functionally convergent but parametrically distinct solutions: Robust degeneracy in a population of computational models of early-birth rat CA1 pyramidal neurons

BackgroundFlexibility and robustness of neuronal function are closely linked to degeneracy, the ability of distinct structural or parametric configurations to produce similar functional outcomes. At the cellular level, this often manifests as ion-channel degeneracy, in which multiple combinations of intrinsic conductances yield comparable electrophysiological phenotypes. MethodologyWe used a population-based, data-driven modelling framework to generate large ensembles of biophysically detailed CA1 pyramidal neuron models constrained by somatic electrophysiological features extracted from patch-clamp recordings in acute slices from early-birth rats. 10 reconstructed morphologies were incorporated, and model populations were analyzed using parameter correlation analysis, principal component analysis, and generalization tests to assess robustness, degeneracy, and morphology dependence of intrinsic properties. ConclusionsAcross the model population, similar somatic firing behaviours emerged from widely different combinations of intrinsic parameters, demonstrating robust two-level ion channel degeneracy both within and across morphologies. Each morphology occupied a distinct region of parameter space, indicating morphology-specific compensatory effects, while weak pairwise parameter correlations suggested distributed compensation rather than tight parameter dependencies. Even with a fixed morphology, multiple parameter subspaces supported comparable electrophysiological phenotypes. Generalization across morphologies was structure-dependent and non-reciprocal, with successful parameter similarity occurring preferentially between structurally similar neurons. Interestingly, to accurately simulate spike-frequency adaptation, it was important to retain some kinetic properties of the ion channel models as free parameters during optimization. Together, these findings show that dendrite morphology shapes the valid parameter space, and similar electrophysiology of CA1 pyramidal neurons arises from the interplay between structural variability and ion-channel diversity. This work highlights the importance of population-based modelling for capturing biological variability and provides insights into how neuronal robustness might be maintained despite substantial heterogeneity, and offers a scalable pipeline for generating biophysically realistic CA1 neuron populations for use in network simulations. Author summaryNeurons must reliably process information even though their internal components, such as ion channels and cellular shape, can vary widely from cell to cell. How stable behaviour emerges from such variability is a fundamental question in neuroscience. In this study, we explored this problem using detailed computer models of early-birth rat hippocampal CA1 pyramidal neurons, a cell type that plays a central role in learning and memory. Instead of building a single "average" neuron model, we created large populations of models that all reproduced key experimental recordings but differed in their internal parameters. We found that neurons with different shapes and different combinations of ion channels could nevertheless generate similar electrical activity. This phenomenon, known as ion channel degeneracy, allows neurons to remain functional despite biological variability or perturbations. Our results show that neuronal shape strongly influences which parameter combinations are viable, but that multiple solutions exist even for the same morphology. The population of models we provide offers a resource for future studies of early-birth CA1 pyramidal cell function and dysfunction.

neuroscience↗

Neuronal degeneracy reflects context-specific trade-offs between energy and information

Among neurons of the same type, the different electrophysiological parameters vary drastically. It is presently unclear if there is any hidden structure in this diversity and how it relates to neuronal function. One potential source of structure is the evolutionary pressure that has sculpted brains to work in an energy-efficient manner. Here we show that neurons parameters do not vary randomly, but that neurons populate a manifold within their parameter space permitting energy-efficient signaling. This manifold represents a Pareto front of degenerate solutions to the problem of energy-efficiency and explains the prevalence of low to intermediate firing rates (2 - 5 Hz) in neocortex. Furthermore, we show that neurons in different sensory brain areas populate different manifolds and that food restriction induces systematic shifts of neuronal parameters along this manifold. Our results suggest that the large diversity of neuronal properties is actually tightly regulated to ensure energy-efficient signaling in different contexts. In briefWe show that there is hidden structure in the diversity of electrophysiological properties of neurons that is governed by trade-offs between energy consumption and information transmission. HighlightsO_LIWe derive an updated neuronal energy budget for a large class of neuron models. C_LIO_LIComputational modeling predicts a manifold of degenerate solutions to energy-efficient information coding forming a Pareto front in the neuronal parameter space. C_LIO_LINeurons from visual and somatosensory cortex fall on the predicted manifold. C_LIO_LIOptimal energy-efficiency is achieved for intermediate-low firing rates (2 - 5 Hz) as observed in neocortex. C_LIO_LIWe observe an energy-efficient form of non-multiplicative synaptic scaling during food deprivation. C_LI O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=164 SRC="FIGDIR/small/708507v2_ufig1.gif" ALT="Figure 1"> View larger version (36K): org.highwire.dtl.DTLVardef@ca6d36org.highwire.dtl.DTLVardef@1c81ca3org.highwire.dtl.DTLVardef@d03833org.highwire.dtl.DTLVardef@19bc7c_HPS_FORMAT_FIGEXP M_FIG C_FIG

neuroscience↗

Cannabinoid CB2R regulates T cell gut-homing in preclinical Crohns model.

Leukocyte trafficking is a critical step in development of chronic intestinal diseases such as Crohns disease. While strategies that block gut-homing have yielded partial success, this disease remains uncurable leaving an unmet clinical need. This is the first paper to describe a role for cannabinoid receptor two (CB2R) signalling in promoting retinoic acid-mediated induction of the gut-homing associated integrin heterodimer 4{beta}7. Using in vitro and in vivo models, we characterised the effects of pharmacological CB2R agonists and inverse agonists on T cell homing receptor expression and transmigration across gut-associated endothelial barriers. This ERK-dependent process coincides with increased T cell adherence in response to CB2R agonism with JWH133. These effects were reversed with an inverse agonist GP-1a in a CB2R dependent manner. Selective deletion of CB2R using CRISPR in vitro or CD4Cre/+ floxed mice in vivo resulted in impaired endothelial cell adherence and decreased diapedesis into the ileal lamina propria. T cell-specific deletion of cnr2, the gene encoding CB2R, attenuated chronic murine ileitis characterised by decreased naive T cell infiltration and loss of tissue architecture in 20wk TNF{Delta}ARE/+mice. This study supports further therapeutic development of CB2R-blocking drugs for the treatment of inflammatory bowel disease.

immunology↗

Centromeric repeat diversity underlies non-Mendelian segregation pattern in hop (Humulus lupulus)

Aberrant meiosis in plants often leads to aneuploidy, genetic instability, and sterility. This can occur due to several factors, including chromosome misalignment, defective synapsis or environmental factors that may result in unusual genetic combinations in the offsprings. Unusual chromosome behavior during male meiosis in Humulus lupulus is linked to irregular chromosome segregation and genome instability. However, the origin of meiotic instability remains unclear. We analyzed the centromeric landscape of H. lupulus to determine its role in aberrant chromosomal segregation during cell division. Using a combination of bioinformatic, molecular and cytogenetic approaches, we identified new centromeric repeats and revealed two types of centromeric organizations. Cytogenetic localization on metaphase chromosomes confirmed the genomic distribution of major repeat arrays and revealed unique features that contribute to aberrant segregation. Two centromeric types are composed of the major repeats SaazCEN and SaazCRM1 which are further accompanied by chromosome-specific centromeric satellites, Saaz40, Saaz293, Saaz85, and HuluTR120. Chromosome 2 displays unbalanced segregation during the cell division, implicating an important role for its centromere structure in segregation patterns. Moreover, Saaz293 is a new marker for studying aneuploidy in hop. Our findings provide new insights on chromosome segregation in hop and highlight the diversity and complexity of the centromere organization in H. lupulus.

plant biology↗

Multi-scale modelling of location- and frequency-dependent synaptic plasticity induced by transcranial magnetic stimulation in the dendrites of pyramidal neurons

BackgroundRepetitive transcranial magnetic stimulation (rTMS) induces long-term changes of synapses, but the mechanisms behind these modifications are not fully understood. Al- though there has been progress in the development of multi-scale modeling tools, no com- prehensive module for simulating rTMS-induced synaptic plasticity in biophysically realistic neurons exists.. ObjectiveWe developed a modelling framework that allows the replication and detailed prediction of long-term changes of excitatory synapses in neurons stimulated by rTMS. MethodsWe implemented a voltage-dependent plasticity model that has been previously established for simulating frequency-, time-, and compartment-dependent spatio-temporal changes of excitatory synapses in neuronal dendrites. The plasticity model can be incorporated into biophysical neuronal models and coupled to electrical field simulations. ResultsWe show that the plasticity modelling framework replicates long-term potentiation (LTP)-like plasticity in hippocampal CA1 pyramidal cells evoked by 10-Hz repetitive magnetic stimulation (rMS). This plasticity was strongly distance dependent and concentrated at the proximal synapses of the neuron. We predicted a decrease in the plasticity amplitude for 5 Hz and 1 Hz protocols with decreasing frequency. Finally, we successfully modelled plasticity in distal synapses upon local electrical theta-burst stimulation (TBS) and predicted proximal and distal plasticity for rMS TBS. Notably, the rMS TBS-evoked synaptic plasticity exhibited robust facilitation by dendritic spikes and low sensitivity to inhibitory suppression. ConclusionThe plasticity modelling framework enables precise simulations of LTP-like cellular effects with high spatio-temporal resolution, enhancing the efficiency of parameter screening and the development of plasticity-inducing rTMS protocols. HighlightsO_LIFirst rigorously validated model of TMS-induced long-term synaptic plasticity in ex- tended neuronal dendrites that goes beyond point-neuron and mean-field modelling C_LIO_LIRobust simulations of experimental data on LTP-like plasticity in the proximal dendrites of CA1 hippocampal pyramidal cells evoked by 10 Hz repetitive magnetic stimulation (rMS) C_LIO_LIReplication of distal synaptic plasticity for a local electrical theta burst stimulation (TBS) protocol C_LIO_LIPrediction of distal and proximal LTP-like plasticity for rMS TBS C_LIO_LI1 Hz rMS does not induce long-term depression C_LI

neuroscience↗

Detection and classification of long terminal repeat sequences in plant LTR-retrotransposons and their analysis using explainable machine learning.

BackgroundLong terminal repeats (LTRs) represent important parts of LTR retrotransposons and retroviruses found in high copy numbers in a majority of eukaryotic genomes. LTRs contain regulatory sequences essential for the life cycle of the retrotransposon. Previous experimental and sequence studies have provided only limited information about LTR structure and composition, mostly from model systems. To enhance our understanding of these key compounds, we focused on the contrasts between LTRs of various retrotransposon families and other genomic regions. Furthermore, this approach can be utilized for the classification and prediction of LTRs. ResultsWe used machine learning methods suitable for DNA sequence classification and applied them to a large dataset of plant LTR retrotransposon sequences. We trained three machine learning models using (i) traditional model ensembles (Gradient Boosting - GBC), (ii) hybrid CNN-LSTM models, and (iii) a pre-trained transformer-based model (DNABERT) using k-mer sequence representation. All three approaches were successful in classifying and isolating LTRs in this data, as well as providing valuable insights into LTR sequence composition. The best classification (expressed as F1 score) achieved for LTR detection was 0.85 using the CNN-LSTM hybrid network model. The most accurate classification task was superfamily classification (F1=0.89) while the least accurate was family classification (F1=0.74). The trained models were subjected to explainability analysis. SHAP positional analysis identified a mixture of interesting features, many of which had a preferred absolute position within the LTR and/or were biologically relevant, such as a centrally positioned TATA-box, and TG..CA patterns around both LTR edges. ConclusionsOur results show that the models used here recognized biologically relevant motifs, such as core promoter elements in the LTR detection task, and a development and stress-related subclass of transcription factor binding sites in the family classification task. Explainability analysis also highlighted the importance of 5- and 3-edges in LTR identity and revealed need to analyze more than just dinucleotides at these ends. Our work shows the applicability of machine learning models to regulatory sequence analysis and classification, and demonstrates the important role of the identified motifs in LTR detection.

bioinformatics↗

Axon morphology and intrinsic cellular properties determine repetitive transcranial magnetic stimulation threshold for plasticity

Repetitive transcranial magnetic stimulation (rTMS) is a widely used therapeutic tool in neurology and psychiatry, but its cellular and molecular mechanisms are not fully understood. Standardizing stimulus parameters, specifically electric field strength and direction, is crucial in experimental and clinical settings. It enables meaningful comparisons across studies and facilitating the translation of findings into clinical practice. However, the impact of biophysical properties inherent to the stimulated neurons and networks on the outcome of rTMS protocols remains not well understood. Consequently, achieving standardization of biological effects across different brain regions and subjects poses a significant challenge. This study compared the effects of 10 Hz repetitive magnetic stimulation (rMS) in entorhino-hippocampal tissue cultures from mice and rats, providing insights into the impact of the same stimulation protocol on similar neuronal networks under standardized conditions. We observed the previously described plastic changes in excitatory and inhibitory synaptic strength of CA1 pyramidal neurons in both mouse and rat tissue cultures, but a higher stimulation intensity was required for the induction of rMS-induced synaptic plasticity in rat tissue cultures. Through systematic comparison of neuronal structural and functional properties and computational modeling, we found that morphological parameters of CA1 pyramidal neurons alone are insufficient to explain the observed differences between the groups. However, axon morphologies of individual cells played a significant role in determining activation thresholds. Notably, differences in intrinsic cellular properties were sufficient to account for the 10 % higher intensity required for the induction of synaptic plasticity in the rat tissue cultures. These findings demonstrate the critical importance of axon morphology and intrinsic cellular properties in predicting the plasticity effects of rTMS, carrying valuable implications for the development of computer models aimed at predicting and standardizing the biological effects of rTMS.

neuroscience↗

The Silene latifolia genome and its giant Y chromosome

In some species, the Y is a tiny chromosome but the dioecious plant Silene latifolia has a giant [~]550 Mb Y chromosome, which has remained unsequenced so far. Here we used a hybrid approach to obtain a high-quality male S. latifolia genome. Using mutants for sexual phenotype, we identified candidate sex-determining genes on the Y. Comparative analysis of the sex chromosomes with outgroups showed the Y is surprisingly rearranged and degenerated for a [~]11 MY-old system. Recombination suppression between X and Y extended in a stepwise process, and triggered a massive accumulation of repeats on the Y, as well as in the non-recombining pericentromeric region of the X, leading to giant sex chromosomes. One-Sentence SummaryThis work uncovers the structure, function, and evolution of one of the largest giant Y chromosomes, that of the model plant Silene latifolia, which is almost 10 times larger than the human Y, despite similar genome sizes.

genomics↗

A biologically inspired repair mechanism for neuronal reconstructions with a focus on human dendrites

Investigating and modelling the functionality of human neurons remains challenging due to the technical limitations, resulting in scarce and incomplete 3D anatomical reconstructions. Here we used a morphological modelling approach based on optimal wiring to repair the parts of a dendritic morphology that were lost due to incomplete tissue samples. In Drosophila, where dendritic regrowth has been studied experimentally using laser ablation, we found that modelling the regrowth reproduced a bimodal distribution between regeneration of cut branches and invasion by neighbouring branches. Interestingly, our repair model followed growth rules similar to those for the generation of a new dendritic tree. To generalise the repair algorithm from Drosophila to mammalian neurons, we artificially sectioned reconstructed dendrites from mouse and human hippocampal pyramidal cell morphologies, and showed that the regrown dendrites were morphologically similar to the original ones. Furthermore, we were able to restore their electrophysiological functionality, as evidenced by the recovery of their firing behaviour. Importantly, we show that such repairs also apply to other neuron types including hippocampal granule cells and cerebellar Purkinje cells. We then extrapolated the repair to incomplete human CA1 pyramidal neurons, where the anatomical boundaries of the particular brain areas innervated by the neurons in question were known. Interestingly, the repair of incomplete human dendrites helped to simulate the recently observed increased synaptic thresholds for dendritic NMDA spikes in human versus mouse dendrites. To make the repair tool available to the neuroscience community, we have developed an intuitive and simple graphical user interface (GUI), which is available in the TREES Toolbox (www.treestoolbox.org). In briefWe use morphological modelling inspired by the regeneration of various artificially cut neuron types and repair incomplete human and nonhuman neuronal dendritic reconstructions. Author summaryReconstructing neuronal dendrites by drawing their 3D branching structures in the computer has proven to be crucial for interpreting the flow of electrical signals and therefore the computations that dendrites implement on their inputs. These reconstructions are tedious and prone to disruptive limitations imposed by experimental procedures. In recent years, complementary computational procedures have emerged that reproduce the fine details of morphology in theoretical models. These models allow, for example, to populate large-scale neural networks and to study structure-function relationships. In this work we use a morphological model based on optimised wiring for signal conduction and material cost to repair faulty reconstructions, in particular those of human hippocampal dendrites, which are rare and precious but often cut due to technical limitations. Interestingly, we find that our synthetic repair mechanism reproduces the two distinct modes of repair observed in real dendrites: regeneration from the severed branch and invasion from neighbouring branches. Our model therefore provides both a useful tool for single-cell electrophysiological simulations and a useful theoretical concept for studying the biology of dendrite repair. HighlightsO_LIOptimal wiring-based growth algorithm replicates regrowth of artificially cut dendrites C_LIO_LIThe growth algorithm repairs cut dendrites in incomplete reconstructions C_LIO_LIThe algorithm works for diverse neuron types in multiple species C_LIO_LIThe repair of morphology restores original electrophysiology C_LIO_LIThe repair of morphology supports simulations of high synaptic thresholds for NMDA spikes in human dendrites C_LIO_LIThe repair tool with user interface is available in the TREES Toolbox C_LI

neuroscience↗

Skewed distribution of spines is independent of presynaptic transmitter release and synaptic plasticity and emerges early during adult neurogenesis

Dendritic spines are crucial for excitatory synaptic transmission as the size of a spine head correlates with the strength of its synapse. The distribution of spine head sizes follows a lognormal-like distribution with more small spines than large ones. We analysed the impact of synaptic activity and plasticity on the spine size distribution in adult-born hippocampal granule cells from rats with induced homo- and heterosynaptic long-term plasticity in vivo and CA1 pyramidal cells from Munc-13-1-Munc13-2 knockout mice with completely blocked synaptic transmission. Neither induction of extrinsic synaptic plasticity nor the blockage of presynaptic activity degrades the lognormal-like distribution but changes its mean, variance and skewness. The skewed distribution develops early in the life of the neuron. Our findings and their computational modelling support the idea that intrinsic synaptic plasticity is sufficient for the generation, while a combination of intrinsic and extrinsic synaptic plasticity maintains lognormal like distribution of spines.

neuroscience↗

Robust and consistent measures of pattern separation based on information theory and demonstrated in the dentate gyrus

Pattern separation is a valuable computational function performed by neuronal circuits, such as the dentate gyrus, where dissimilarity between inputs is increased, reducing noise and increasing the storage capacity of downstream networks. Pattern separation is studied from both in vivo experimental and computational perspectives and, a number of different measures (such as orthogonalisation, decorrelation, or spike train distance) have been applied to quantify the process of pattern separation. However, these are known to give conclusions that can differ qualitatively depending on the choice of measure and the parameters used to calculate it. We here demonstrate that arbitrarily increasing sparsity, a noticeable feature of dentate granule cell firing and one that is believed to be key to pattern separation, typically leads to improved classical measures for pattern separation even, inappropriately, up to the point where almost all information about the inputs is lost. Standard measures therefore both cannot differentiate between pattern separation and pattern destruction, and give results that may depend on arbitrary parameter choices. We propose that techniques from information theory, in particular mutual information, transfer entropy, and redundancy, should be applied to penalise the potential for lost information (often due to increased sparsity) that is neglected by existing measures. We compare five commonly-used measures of pattern separation with three novel techniques based on information theory, showing that the latter can be applied in a principled way and provide a robust and reliable measure for comparing the pattern separation performance of different neurons and networks. We demonstrate our new measures on detailed compartmental models of individual dentate granule cells and a dentate microcircuit, and show how structural changes associated with epilepsy affect pattern separation performance. We also demonstrate how our measures of pattern separation can predict pattern completion accuracy. Overall, our measures solve a widely acknowledged problem in assessing the pattern separation of neural circuits such as the dentate gyrus, as well as the cerebellum and mushroom body. Finally we provide a publicly available toolbox allowing for easy analysis of pattern separation in spike train ensembles. Author summaryThe hippocampus is a region of the brain strongly associated with spatial navigation and encoding of episodic memories. To perform these functions effectively it makes use of circuits that perform pattern separation, where redundant structure is removed from neural representations leaving only the most salient information. Pattern separation allows downstream pattern completion networks to better distinguish between similar situations. Pathological changes, caused by Alzheimers, schizophrenia, or epilepsy, to the circuits that perform pattern separation are associated with reduced discriminative ability in both animal models and humans. Traditionally, pattern separation has been described alongside the complementary process of pattern completion, but more recent studies have focussed on the detailed neuronal and circuit features that contribute to pattern separation alone. We here show that traditional measures of pattern separation are inappropriate in this case, as they do not give consistent conclusions when parameters are changed and can confound pattern separation with the loss of important information. We show that directly accounting for the information throughput of a pattern separation circuit can provide new measures of pattern separation that are robust and consistent, and allow for nuanced analysis of the structure-function relationship of such circuits and how this may be perturbed by pathology.

neuroscience↗

The amyloid precursor protein regulates synaptic transmission at medial perforant path synapses

The perforant path provides the main cortical excitatory input to the hippocampus. Due to its important role in information processing and coding, entorhinal projections to the dentate gyrus have been studied in considerable detail. Nevertheless, a characterization of synaptic transmission between individual connected pairs of entorhinal stellate cells and dentate granule cells is still pending. Here, we have used organotypic entorhino-hippocampal tissue cultures, in which the entorhino-dentate (EC-GC) projection is present and EC-GC pairs can be studied using whole-cell patch clamp recordings. Using cultures of wildtype mice, the properties of EC-GC synapses formed by afferents from the lateral and medial entorhinal cortex were compared and differences in short-term plasticity were revealed. Since the perforant path is severely affected in Alzheimers disease, we used cultures of APP-deficient mice to address the role of the amyloid-precursor protein (APP) at this synapse. APP-deficiency caused alterations in excitatory neurotransmission at medial perforant path synapses that were accompanied by transcriptomic and ultrastructural changes. Moreover, the deletion of pre- but not postsynaptic APP through the local injection of Cre-expressing AAVs in conditional APPflox/flox tissue cultures increased the efficacy of neurotransmission at perforant path synapses. Together, these data suggest a physiological role for presynaptic APP at medial perforant path synapses, which may be adversely affected under conditions of altered APP processing.

neuroscience↗