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Regulation of Synapse Development by Activity Dependent Transcription in Inhibitory NeuronsMardinly, Alan Robert 07 June 2014 (has links)
Neuronal activity and subsequent calcium influx activates a signaling cascade that causes transcription factors in the nucleus to rapidly induce an early-response program of gene expression. This early-response program is composed of transcriptional regulators that in turn induce transcription of late-response genes, which are enriched for regulators of synaptic development and plasticity that act locally at the synapse.
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The TREM2 Receptor Directs Microglial Activity in Neurodegeneration and NeurodevelopmentJay, Taylor Reagan January 2019 (has links)
No description available.
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Mechanisms Shaping Excitatory Transmission at the Developing Retinogeniculate SynapseHauser, Jessica Lauren 22 October 2014 (has links)
The retinogeniculate synapse, the connection between retinal ganglion cells (RGCs) and thalamic relay neurons, undergoes extensive remodeling and refinement in the first few postnatal weeks. While many studies have focused on this process, little is known about the factors that influence excitatory transmission during this dynamic period. A major goal of my dissertation research was to identify mechanisms that regulate glutamate release and clearance at the developing synapse. First, we investigated the role of glutamate transporters and metabotropic glutamate receptors (mGluRs) in shaping excitatory transmission. Early in development, we found presynaptic group II/III mGluRs are present and are activated by glutamate released from RGCs following optic tract stimulation at natural frequencies. This response was found to diminish with age, but glutamate transporters continued to shape synaptic currents throughout development. The finding that glutamate is able to escape the synaptic cleft and bind extrasynaptic high-affinity mGluRs led us to speculate that glutamate might also diffuse to neighboring synapses and bind ionotropic glutamate receptors opposing quiescent release sites. Excitatory currents recorded from immature, but not mature, retinogeniculate synapses display a prolonged decay timecourse. We found evidence that both asynchronous release of glutamate as well as spillover of glutamate between neighboring synapses contributes to these slowly decaying synaptic currents. Furthermore, we uncovered and characterized a novel, purely spillover-mediated current from immature relay neurons, which strongly supports the presence of glutamate spillover between boutons of different RGCs. The results of my studies indicate that far more RGCs contribute to relay neuron firing than would be predicted by the anatomy alone. Finally, in an ongoing study, we investigated the functional role of the neuronal glutamate transporter GLT-1 at the immature retinogeniculate synapse. While GLT-1 has been found in both neurons and glia, excitatory currents at the retinogeniculate synapse were largely unaffected in mice lacking neuronal GLT-1, suggesting non-neuronal glutamate transporters are responsible for the majority of glutamate removal from the developing synapse. Taken together, these results provide insight into the synaptic environment of the developing retinogeniculate synapse and identify a number of mechanisms that shape excitatory transmission during this period of synaptic maturation and refinement.
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Pannexin 1 regulates dendritic spines in developing cortical neuronsSanchez-Arias, Juan C. 04 May 2020 (has links)
Sensory, cognitive, and emotional processing are rooted in the cerebral cortex. The cerebral cortex is comprised of six layers defined by the neurons within them that have distinctive connection, both within cortex itself and with other subcortical structures. Although still far from solving the mysteries of the mind, it is clear that networks form by neurons in the cerebral cortex provide the computational substrate for a remarkable range of behaviours. This neuron to neuron activation is mediated through dendritic spines, the postsynaptic target of most excitatory synapses in the cerebral cortex. Dendritic spines are small protrusions found along dendrites of neurons, and their number, as well as structural changes, accompany the development of synapses and establishment of neuronal networks. In fact, dendritic spines undergo rapid structural and functional changes guided by neuronal activity. This marriage between structural and functional plasticity, makes dendritic spines crucial in fine-tuning of networks in the brain; not surprisingly, dendritic spine aberrations are a hallmark of multiple neurodevelopmental, neuropsychiatric, and neurodegenerative disorders. With this in mind, I considered Pannexin 1 (Panx1) an interesting novel candidate for a regulatory role on cortical neuronal network and dendritic spine development, for the following reasons. First, Panx1 transcripts are enriched in the brain and in the cortex are most abundant during the embryonic and early postnatal period. . This timing roughly corresponds to a period of synaptogenesis in the postnatal brain. Second, Panx1 localizes to postsynaptic compartments in neurons and its disruption leads to enhance excitability and potentiation of neuron-to neuron communication. Third, disruption of Panx1 (either knockdown or pharmacological blockade) leads to neurite outgrowth in neuron-like cells. Lastly, genetic variants in PANX1 have been associated with neurodevelopmental disorders. This dissertation explores the role of Panx1 in the development of dendritic spines and neuronal networks, furthering our understanding on cortical development and placing Panx1 as a novel regulator of structural and functional plasticity in the brain.
Chapter 1 discusses core concepts on cortical development, with an emphasis on pyramidal neuron, the most abundant and only known projection neurons in the cerebral cortex. Here, I review the embryonic origin of pyramidal neurons, their postnasal development, and how cortical circuits are assembled. I finish this chapter with a brief review on Panx1 and its known expression and involvement in neuronal function.
In Chapter 2 I explore the functional properties of neuronal networks and synaptic composition of cortical neurons in the absence of Panx1. Using live cell imaging and analysis of Ca2+ transients in dense primary cortical cultures, revealed that Panx1 knock-out (KO) cultures exhibit more and larger groups of significantly co-activated neurons, known as network ensembles. These network properties were not explained by differences in cell viability or cell-type composition. Examination of protein expression from cortical synaptosome preparations revealed that Panx1 is enriched in synaptic compartments, while also confirming a developmental downregulation. This analysis also revealed increased levels of the postsynaptic scaffolding protein PSD-95, along with the postsynaptic glutamate receptors GluA1 and GluN2A. Lastly, ex vivo tracing of dendritic spines on apical dendrites of Layer 5 pyramidal neurons in global and glutamatergic-specific Panx1 KO brain slices revealed higher spine densities in early and late postnatal development, with no differences in spine length. Analysis of dendritic spine densities in fixed cultured cortical neurons revealed an increase associated with Panx1 KO. Altogether, this work presents for the first time a connection between Panx1 and structural development of dendritic spines and suggest that Panx1 regulates cortical neuronal networks through changes in spine density.
Chapter 3 examines the influence of Panx1 on spiny protrusions growth and movement. Spiny protrusion are long, thin, highly dynamic spine precursors. Taking advantage of a fluorescent signal localized to the plasma membrane, I visualized spiny protrusions and quantified their dynamics in wildtype (WT) and Panx1 KO developing cortical neurons, both under fixed and live conditions. I found that transient Panx1 expression is associated with decreased spiny protrusion density both in WT and Panx1 KO neurons. Using live cell imaging, I found that spiny protrusions are more stable and less motile in Panx1 KO neurons, while its transient expression reversed both of these phenotypes. These results suggest that Panx1 regulation of dendritic spines development is rooted partly in the regulation of spiny protrusion dynamics.
Overall, this dissertation demonstrates that Panx1 negatively regulates dendritic spines in part by influencing spiny protrusion dynamics. It is reasonable to speculate that Panx1 regulation of dendritic spines underlies its newly discovered role in the formation network ensembles, providing a putative mechanism for previously described roles of Panx1 in synaptic plasticity. Likewise, this body of work furthers our understanding of Panx1 by filling some of the gaps attached to its developmental expression and association with neurodevelopmental disease. / Graduate / 2021-04-16
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BDNF and Astrocyte TrkB.T1 Signaling as a Mechanism Underlying Astrocyte Synapse Interactions in Motor and Barrel CortexPinkston, Beatriz T. Ceja 25 July 2024 (has links)
Synapses are the fundamental units of communication in the brain, and their proper development and function are critical for cognitive processes and behavior. While the development of glutamatergic synapses has been extensively studied, the mechanisms underlying the formation of the tripartite synapse remain poorly understood. The tripartite synapse is a specialized structure consisting of the presynaptic terminal, the postsynaptic element, and a perisynaptic astrocyte process (PAP) that ensheathes the synaptic cleft. Increasing evidence demonstrates that PAPs are critical for synapse formation, stabilization, and plasticity. However, the mechanisms that govern the formation of tripartite synapses remain to be fully elucidated.
This dissertation investigates the role of the astrocyte TrkB.T1 receptor, a truncated isoform of the canonical receptor for brain derived neurotrophic factor (BDNF), in mediating behavior and excitatory synapse development. Using an astrocyte-specific conditional TrkB.T1 knockout mouse model, we demonstrate that deletion of TrkB.T1 results in hyperactive locomotion, with increased voluntary running and perseverative motor behaviors. Through a combination of molecular and cellular approaches, we demonstrate that the behavioral abnormalities that result from TrkB.T1 deletion are accompanied by developmental reductions in glutamatergic synapses and astrocyte-synapse interactions in the motor and barrel cortex. Mechanistic studies using neuron-astrocyte co-cultures also reveal that loss of TrkB.T1 in astrocytes inhibits the formation of PAPs around glutamatergic synapses.
Altogether, the insights presented herein present a novel astrocyte-mediated signaling mechanism that regulates excitatory synapse formation. These insights have important implications for understanding both neurodevelopmental and neuropsychiatric disorders involving synaptic dysfunction. / Doctor of Philosophy / Synapses are the central unit of communication in the brain. These neurochemical hubs of communication are able to orchestrate systems and overall behavior. Classically, a synapse has been defined as the contact point of communication between a pre-synaptic terminal and an apposing post-synaptic element. Simply illustrated, pre-synaptic terminals release neurotransmitters that can bind to the receptors of post-synaptic elements, enabling for either excitatory or inhibitory communication. While the field of neuroscience has studied how synapses form and mature, there are still many unanswered questions about a specialized synaptic structure called the tripartite synapse.
The tripartite synapse involves not just a pre- and post-synaptic element, but also a third player – a multitasking cell called the astrocyte. Astrocytes extend thousands of fine, leaflet-like processes that wrap around and support neuronal synapses. These processes, termed perisynaptic astrocyte processes (PAPs), are critical for synaptic development and function.
This dissertation investigated how brain derived neurotrophic factor (BDNF) and its receptor TrkB.T1, found almost exclusively in astrocytes, control the formation of PAPs during brain development. Using a combination of advanced microscopy and cellular and molecular techniques, we demonstrate that BDNF/TrkB.T1 signaling in astrocytes acts as a critical regulator in the development of synapses and astrocyte-synapse interactions, instructing astrocytes to extend processes that can ensheath synapses as they mature. Disruption of this pathway in mice also led to hyperactive behavior, underscoring its importance for proper brain development and function.
This novel astrocyte-based mechanism governing synapse maturation has important implications for understanding neurodevelopmental and neuropsychiatric disorders and could ultimately lead to novel therapeutic strategies targeting synaptic defects in these conditions.
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Role of the cotransporter KCC2 in cortical excitatory synapse development and febrile seizure susceptibilityAwad, Patricia Nora 08 1900 (has links)
Le co-transporteur KCC2 spécifique au potassium et chlore a pour rôle principal de réduire la concentration intracellulaire de chlore, entraînant l’hyperpolarisation des courants GABAergic l’autorisant ainsi à devenir inhibiteur dans le cerveau mature. De plus, il est aussi impliqué dans le développement des synapses excitatrices, nommées aussi les épines dendritiques. Le but de notre projet est d’étudier l’effet des modifications concernant l'expression et la fonction de KCC2 dans le cortex du cerveau en développement dans un contexte de convulsions précoces.
Les convulsions fébriles affectent environ 5% des enfants, et ce dès la première année de vie. Les enfants atteints de convulsions fébriles prolongées et atypiques sont plus susceptibles à développer l’épilepsie. De plus, la présence d’une malformation cérébrale prédispose au développement de convulsions fébriles atypiques, et d’épilepsie du lobe temporal. Ceci suggère que ces pathologies néonatales peuvent altérer le développement des circuits neuronaux irréversiblement. Cependant, les mécanismes qui sous-tendent ces effets ne sont pas encore compris. Nous avons pour but de comprendre l'impact des altérations de KCC2 sur la survenue des convulsions et dans la formation des épines dendritiques.
Nous avons étudié KCC2 dans un modèle animal de convulsions précédemment validé, qui combine une lésion corticale à P1 (premier jour de vie postnatale), suivie d'une convulsion induite par hyperthermie à P10 (nommés rats LHS). À la suite de ces insultes, 86% des rats mâles LHS développent l’épilepsie à l’âge adulte, au même titre que des troubles d’apprentissage. À P20, ces animaux presentent une augmentation de l'expression de KCC2 associée à une hyperpolarisation du potentiel de réversion de GABA. De plus, nous avons observé des réductions dans la taille des épines dendritiques et l'amplitude des courants post-synaptiques excitateurs miniatures, ainsi qu’un déficit de mémoire spatial, et ce avant le développement des convulsions spontanées. Dans le but de rétablir les déficits observés chez les rats LHS, nous avons alors réalisé un knock-down de KCC2 par shARN spécifique par électroporation in utero. Nos résultats ont montré une diminution de la susceptibilité aux convulsions due à la lésion corticale, ainsi qu'une restauration de la taille des épines. Ainsi, l’augmentation de KCC2 à la suite d'une convulsion précoce, augmente la susceptibilité aux convulsions modifiant la morphologie des épines dendritiques, probable facteur contribuant à l’atrophie de l’hippocampe et l’occurrence des déficits cognitifs.
Le deuxième objectif a été d'inspecter l’effet de la surexpression précoce de KCC2 dans le développement des épines dendritiques de l’hippocampe. Nous avons ainsi surexprimé KCC2 aussi bien in vitro dans des cultures organotypiques d’hippocampe, qu' in vivo par électroporation in utero. À l'inverse des résultats publiés dans le cortex, nous avons observé une diminution de la densité d’épines dendritiques et une augmentation de la taille des épines. Afin de confirmer la spécificité du rôle de KCC2 face à la région néocorticale étudiée, nous avons surexprimé KCC2 dans le cortex par électroporation in utero. Cette manipulation a eu pour conséquences d’augmenter la densité et la longueur des épines synaptiques de l’arbre dendritique des cellules glutamatergiques. En conséquent, ces résultats ont démontré pour la première fois, que les modifications de l’expression de KCC2 sont spécifiques à la région affectée. Ceci souligne les obstacles auxquels nous faisons face dans le développement de thérapie adéquat pour l’épilepsie ayant pour but de moduler l’expression de KCC2 de façon spécifique. / The potassium-chloride cotransporter KCC2 decreases intracellular Cl- levels and renders GABA responses inhibitory. In addition, it has also been shown to modulate excitatory synapse development. In this project, we investigated how alterations of KCC2 expression levels affect these two key processes in cortical structures of a normal and/or epileptic developing brain.
First, we demonstrate that KCC2 expression is altered by early-life febrile status epilepticus. Febrile seizures affect about 5% of children during the first year of life. Atypical febrile seizures, particularly febrile status epilepticus, correlate with a higher risk of developing cognitive deficits and temporal lobe epilepsy as adults, suggesting that they may permanently change the developmental trajectory of neuronal circuits. In fact, the presence of a cerebral malformation predisposes to the development of atypical febrile seizures and temporal lobe epilepsy. The mechanisms underlying these effects are not clear. Here, we investigated the functional impact of this alteration on subsequent synapse formation and seizure susceptibility.
We analyzed KCC2 expression and spine density in the hippocampus of a well-established rodent model of atypical febrile seizures, combining a cortical freeze lesion at post-natal day 1 (P1) and hyperthermia-induced seizure at P10 (LHS rats). 86% of these LHS males develop epilepsy and learning and memory deficits in adulthood. At P20, we found a precocious increase in KCC2 protein levels, accompanied by a negative shift of the reversal potential of GABA (EGABA) by gramicidin-perforated patch. In parallel, we observed a reduction in dendritic spine size by DiI labelling and a reduction of miniature excitatory postsynaptic current (mEPSC) amplitude in CA1 pyramidal neurons, as well as impaired spatial memory. To investigate whether the premature expression of KCC2 played a role in these alterations in the LHS model, and on seizure susceptibility, we reduced KCC2 expression in CA1 pyramidal neurons by in utero electroporation of shRNA using a triple-probe electrode. This approach lead to reduced febrile seizure susceptibility, and rescued spine size shrinkage in LHS rats. Our results show that an increase of KCC2 levels induced by early-life insults affect seizure susceptibility and spine development and may be a contributing factor to the occurrence of hippocampal atrophy and associated cognitive deficits in LHS rats.
Second, we investigated whether KCC2 premature overexpression plays a role in spine alterations in the hippocampus. We overexpressed KCC2 in hippocampal organotypic cultures by biolistic transfection and in vivo by in utero electroporation. In contrast to what was previously published, we observed that both manipulations lead to a decrease in spine density in the hippocampus, as well as an increase in spine head size in vivo. In fact, it has been previously shown that overexpressing KCC2 leads to an increase of spine density in the cortex in vivo. To prove that this discrepancy is due to brain regional differences, we overexpressed KCC2 in the cortex by in utero electroporation, and similarly found an increase in spine density and length. Altogether, our results demonstrate for the first time, that alterations of KCC2 expression are brain circuit-specific. These findings highlights the obstacles we will face to find adequate pharmacological treatment to specifically modulate KCC2 in a region-specific and time-sensitive manner in epilepsy.
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