Biology subjects

Kentros, C.

Publications and source records attributed to Kentros, C..

9 recordsLinked to original sources

bioRxiv2026

Reproducible and predictable reorganization of place fields driven by grid subfield rate changes

Understanding how the brain constructs stable yet flexible maps of space remains a central challenge in neuroscience. Place cells in the hippocampus fire at specific locations in a given environment, but reorganize completely upon introduction to another environment in a process called remapping. The medial entorhinal cortex (MEC) provides a major cortical input to the hippocampus, and the spatially periodic firing patterns of its grid cells are thought to contribute to place field formation. We previously showed that chemogenetic depolarization of MEC layer II stellate cells selectively altered firing rates within individual grid cell subfields, impaired spatial memory, and induced a form of reversible place cell remapping that we called artificial remapping. However, it remains unclear whether artificial remapping reflects a reproducible and stable mapping from entorhinal inputs to place cell outputs or a random reorganization of place fields. To explore the transfer of information between MEC and hippocampus, we repeated this chemogenetic manipulation on consecutive days and found that stimulating the same stellate cells produced similar changes in both grid subfield rates and place field locations. Using both experimental and simulated data, we show that baseline place cell activity patterns could be used to predict place field locations following the manipulation. These findings provide direct evidence for consistent input-output relationships in the entorhinal-hippocampal system and point to a central role for grid subfield rate changes in the reorganization of hippocampal spatial representations.

neuroscience↗

bioRxiv2026

Preferential generation of pathological tau species in specific subtypes of entorhinal neurons: implications for Alzheimer's Disease.

Alzheimers Disease (AD) is distinguished by the presence of two key pathological features: amyloid plaques, accumulations of proteolytic products of Amyloid Precursor Protein, and neurofibrillary tangles (NFTs), intracellular aggregations of microtubule-associated protein tau. NFTs first appear in particular entorhinal cortex (EC) neurons (called pre-alpha neurons) in asymptomatic patients, then continue to spread through other connected brain regions as the disease progresses. This stereotypical progression of tauopathy through synaptically connected brain regions (i.e. Braak stages) not only suggests that the tauopathy in AD spreads transsynaptically, it also raises the question whether particular neuronal subtypes and/or brain regions are especially prone to tauopathy. We explored this question by overexpressing wildtype human tau protein (hTau) in a variety of entorhinal and neocortical neuronal subtypes. We then compared the tendencies of different neuronal cell types to develop different pathological tau species over time and found that tau pathology does indeed develop at markedly different rates in different neuronal subtypes. Perhaps unsurprisingly, the EC is particularly prone, with the likely rat cognates of the pre-alpha neurons (ECLII fan cells) among the first to express pathological tau label. Fan cells were not, however, the neurons with the greatest vulnerability to generate pathological tau species: subsets of ECLIII neurons were found to express disproportional amounts of pathological tau. This is of particular interest given that the next structures to develop AD-related tauopathy after the EC in patients are CA1 hippocampus and subiculum, where ECLIII neurons project, rather than the dentate gyrus and CA3, where ECLII fan cells project. These results demonstrate differential susceptibility of different neuronal subtypes to pathological tau species and suggest distinct roles for different entorhinal neuronal subtypes in the propagation of the tauopathy underlying AD-related neurodegeneration.

neuroscience↗

bioRxiv2026

Heterogeneous single-cell dynamics support stable population codes for objects in the mouse anterior cingulate cortex

Remembering object locations is crucial for survival, yet how the anterior cingulate cortex (ACC) encodes spatial features across repeated experiences has not been fully characterized. Using longitudinal calcium imaging in freely moving mice, we tracked excitatory ACC neurons while animals explored objects across multiple days. We demonstrate that the ACC employs a highly dynamic coding strategy: while the overall proportion of object-responsive neurons remains constant across sessions, the specific identities of these cells fluctuate, showing a continuous turnover alongside a small, stable core. This dynamic coding is modulated by behavior, with high-exploring mice exhibiting greater cellular stability. Crucially, population-level analyses reveal that stable spatial representations emerge from collective dynamics rather than fixed single-cell identities. Population decoding demonstrates that information becomes linearly separable and highly efficient at a coarser ensemble scale. Thus, the ACC achieves representational stability through emergent network organization despite persistent single-cell dynamics.

neuroscience↗

bioRxiv2023

Direct Entorhinal Control of CA1 Temporal Coding

During behavior, hippocampal neurons fire in consistent theta sequences, organized by the theta rhythm, which have been linked to predictive coding of future actions. The mechanisms of sequence generation are yet unclear, but in the hippocampal CA1 subfield, are thought to involve both major input streams into CA1 neurons, from CA3 pyramidal neurons and directly from entorhinal cortex. We disentangled the role of these two afferent input with highly specific optogenetic inhibition limited to the direct entorhinal afferents of CA1, thereby leaving the rest of the hippocampal-entorhinal circuit intact. While CA1 spatial firing properties were largely unaffected, theta phase precession was largely abolished. Surprisingly, while theta phase precession is thought to generate theta sequences, theta sequences were actually strengthened when it was suppressed. These results suggest that sequence generation is internal to the hippocampus, while the entorhinal inputs may act as a supervisory signal driving learning and representational updates.

neuroscience↗

bioRxiv2022

Lowering levels of reelin in entorhinal cortex layer II-neurons results in lowered levels of intracellular amyloid-β.

Projection neurons in the anterolateral part of entorhinal cortex layer II (alEC LII) are the predominant cortical site for hyperphosphorylation of tau (p-tau) and formation of neurofibrillary tangles (NFTs) in brains of subjects with early-stage Alzheimers Disease (AD). A majority of alEC LII-neurons are unique among cortical excitatory neurons by expressing the protein reelin (Re+). In AD patients, and a rat model for AD overexpression mutated human APP, these Re+ excitatory projection-neurons are prone to accumulate intracellular amyloid-{beta} (iA{beta}). Biochemical pathways that involve reelin-signaling regulate levels of p-tau, and iA{beta} has been shown to impair such reelin-signaling. We therefore used the rat model and set out to assess whether accumulation of iA{beta} in Re+ alEC LII projection neurons relates to the fact that these neurons express reelin. Here we show that in Re+ alEC LII-neurons, reelin and iA{beta}42 engage in a direct protein-protein interaction, and that microRNA-mediated lowering of reelin-levels in these neurons leads to a concomitant reduction of non-fibrillar iA{beta} ranging across three levels of aggregation. Our experiments are carried out several months before plaque pathology emerges in the rat model, and the reduction of iA{beta} occurs without any substantial associated changes in human APP-levels. We propose a model positioning reelin in a sequence of changes in functional pathways in Re+ alEC LII-neurons, explaining the region and neuron-specific initiation of AD pathology. SignificanceAnterolateral entorhinal cortex layer II (EC LII) neurons are the predominant cortical site for hyperphosphorylation of tau (p-tau) and formation of neurofibrillary tangles (NFTs) in brains of subjects with early-stage Alzheimers disease (AD). The same neurons are prone to very early accumulation of non-fibrillary forms of amyloid-{beta} in the context of AD, and are unique among cortical excitatory neurons by expressing the protein reelin. We show that in such alEC LII-neurons, reelin and iA{beta}42 engage in a direct protein-protein interaction, and that selectively lowering levels of reelin leads to a concomitant reduction of non-fibrillar A{beta}. We propose a model positioning reelin in a sequence of changes in functional pathways in reelin-expressing EC LII neurons, explaining the region and neuron specific initiation of AD.

pathology↗

bioRxiv2020

Local circuits of layer Vb-to-Va neurons mediate hippocampal-cortical outputs in lateral but not in medial entorhinal cortex

The entorhinal cortex, in particular neurons in layer V, allegedly mediate transfer of information from the hippocampus to the neocortex, underlying long-term memory. Recently, this circuit has been shown to comprise a hippocampal output recipient layer Vb and a cortical projecting layer Va. With the use of in vitro electrophysiology in transgenic mice specific for layer Vb, we assessed the presence of the thus necessary connection from layer Vb-to-Va in the functionally distinct medial (MEC) and lateral (LEC) subdivisions; MEC, particularly its dorsal part, processes allocentric spatial information, whereas the corresponding part of LEC processes information representing elements of episodes. Using identical experimental approaches, we show that connections from layer Vb-to-Va neurons are more effective in LEC compared with dorsal MEC. This indicates that the hippocampal-cortex output circuit is more effective in LEC, suggesting that episodic systems-consolidation may use LEC-derived information more than allocentric spatial information from MEC.

neuroscience↗

bioRxiv2019

Modelling functional human neuromuscular junctions in a differentially-perturbable microfluidic environment, validated through recombinant monosynaptic pseudotyped ΔG-rabies virus tracing

Compartmentalized microfluidic culture systems provide new perspectives in in vitro disease modelling as they enable co-culture of different relevant cell types in interconnected but fluidically isolated microenvironments. Such systems are thus particularly interesting in the context of in vitro modelling of mechanistic aspects of neurodegenerative diseases such as amyotrophic lateral sclerosis, which progressively affect the function of neuromuscular junctions, as they enable the co-culture of motor neurons and muscle cells in separate, but interconnected compartments. In combination with cell reprogramming technologies for the generation of human (including patient-specific) motor neurons, microfluidic platforms can thus become important research tools in preclinical studies. In this study, we present the application of a microfluidic chip with a differentially-perturbable microenvironment as a platform for establishing functional neuromuscular junctions using human induced pluripotent stem cell derived motor neurons and human myotubes. As a novel approach, we demonstrate the functionality of the platform using a designer pseudotyped {Delta}G-rabies virus for retrograde monosynaptic tracing.\n\nGraphical abstract\n\nO_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=186 SRC=\"FIGDIR/small/745513v1_ufig1.gif\" ALT=\"Figure 1\">\nView larger version (91K):\norg.highwire.dtl.DTLVardef@d34487org.highwire.dtl.DTLVardef@3804b8org.highwire.dtl.DTLVardef@1be0389org.highwire.dtl.DTLVardef@1da414c_HPS_FORMAT_FIGEXP M_FIG Functional neuromuscular junction in a microfluidic chip\n\n(a) Overview of microfluidic chip. Human iPS cell-derived motor neuron aggregates (spheroids indicated by black arrows) are seeded in the three lateral compartments of the chip, while human myotubes (white arrows) are seeded in the middle compartment.\n\n(b) Directed connectivity and retrograde virus tracing. Outgrowing axons (yellow arrow) from the motor neuron aggregate enter the directional axon tunnels (grey rectangles) and form connections with the myotubes (white arrow) within the opposite compartment. Addition of a designer monosynaptic pseudotyped {Delta}G-rabies virus to the myotube compartment, infects the myotubes (green) expressing an exogenous receptor (TVA) and rabies glycoprotein (G), subsequently making infectious viruses that are retrogradely transported through the motor neuron axons (green arrow) back to the neuronal cell bodies within the aggregate, validating neuromuscular junction functionality.\n\nC_FIG

neuroscience↗

bioRxiv2019

Generation of viral vectors specific to neuronal subtypes of targeted brain regions by Enhancer-Driven Gene Expression (EDGE)

Understanding brain function requires understanding neural circuits at the level of specificity at which they operate. While recent years have seen the development of a variety of remarkable molecular tools for the study of neural circuits, their utility is currently limited by the inability to deploy them in specific elements of native neural circuits, i.e. particular neuronal subtypes. One can obtain a degree of specificity with neuron-specific promoters, but native promoters are almost never sufficiently specific restricting this approach to transgenic animals. We recently showed that one can obtain transgenic mice with augmented anatomical specificity in targeted brain regions by identifying cis-regulatory elements (i.e. enhancers) uniquely active in those brain regions and combining them with a heterologous promoter, an approach we call EDGE (Enhancer-Driven Gene Expression). Here we extend this strategy to the generation of viral (rAAV) vectors, showing that when combined with the right minimal promoter they largely recapitulate the specificity seen in the corresponding transgenic lines in wildtype animals, even of another species. Because active enhancers can be identified in any tissue sample, this approach promises to enable the kind of circuit-specific manipulations in any species. This should not only greatly enhance our understanding of brain function, but may one day even provide novel therapeutic avenues to correct the imbalances in neural circuits underlying many disorders of the brain.

neuroscience↗

bioRxiv2018

The marked diversity of unique cortical enhancers enables the generation of neuron-specific tools by Enhancer-Driven Gene Expression (EDGE)

Understanding neural circuit function requires individually addressing their component parts: specific neuronal cell types. However, not only do the precise genetic mechanisms specifying neuronal cell types remain obscure, access to these neuronal cell types by transgenic techniques also remains elusive. While most genes are expressed in the brain, the vast majority are expressed in many different kinds of neurons, suggesting that promoters alone are not sufficiently specific to distinguish cell types. However, there are orders of magnitude more distal genetic cis-regulatory elements controlling transcription (i.e. enhancers), so we screened for enhancer activity in microdissected samples of mouse cortical subregions. This identified thousands of novel putative enhancers, many unique to particular cortical subregions. Pronuclear injection of expression constructs containing such region-specific enhancers resulted in transgenic lines driving expression in distinct sets of cells specifically in the targeted cortical subregions, even though the parent genes promoter was relatively nonspecific. These data showcase the promise of utilizing the genetic mechanisms underlying the specification of diverse neuronal cell types for the development of genetic tools potentially capable of targeting any neuronal circuit of interest, an approach we call Enhancer-Driven Gene Expression (EDGE).\n\nHighlightsO_LIEnhancer ChIP-seq of cortical subregions reveals 59372 putative enhancers.\nC_LIO_LI3740 of these are specific to particular cortical subregions.\nC_LIO_LIThis reflects the remarkable anatomical diversity of the adult cortex.\nC_LIO_LIUnique enhancers provide a means to make targeted cell-type specific genetic tools.\nC_LI

neuroscience↗