22 results on '"Mack, Volker"'
Search Results
2. CKAMP44: A Brain-Specific Protein Attenuating Short-Term Synaptic Plasticity in the Dentate Gyms
- Author
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von Engelhardt, Jakob, Mack, Volker, Sprengel, Rolf, Kavenstock, Netta, Li, Ka Wan, Stern-Bach, Yael, Smit, August B., Seeburg, Peter H., and Monyer, Hannah
- Published
- 2010
- Full Text
- View/download PDF
3. Impaired Reproductive Behavior by Lack of GluR-B Containing AMPA Receptors But Not of NMDA Receptors in Hypothalamic and Septal Neurons
- Author
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Shimshek, Derya R., Bus, Thorsten, Grinevich, Valery, Single, Frank N., Mack, Volker, Sprengel, Rolf, Spergel, Daniel J., and Seeburg, Peter H.
- Published
- 2006
4. Differential GABAA receptor clustering determines GABA synapse plasticity in rat oxytocin neurons around parturition and the onset of lactation
- Author
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Koksma, Jan-Jurjen, Fritschy, Jean-Marc, Mack, Volker, Van Kesteren, Ronald E., and Brussaard, Arjen B.
- Published
- 2005
- Full Text
- View/download PDF
5. Dominance of the lurcher mutation in heteromeric kainate and AMPA receptor channels
- Author
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Schwarz, Martin K., Pawlak, Verena, Osten, Pavel, Mack, Volker, Seeburg, Peter H., and Köhr, Georg
- Published
- 2001
- Full Text
- View/download PDF
6. State-dependent Ras signalling and AMPA receptor trafficking
- Author
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Yi Qin, Yinghua Zhu, Baumgart, Joel P., Stornetta, Ruth L., Seidenman, Kennet, Mack, Volker, Aelst, Linda van, and Zhu, J. Julius
- Subjects
Phosphorylation -- Analysis ,Adaptation (Physiology) -- Influence ,Adaptation (Physiology) -- Research ,Neural transmission -- Research ,Cognition in children -- Research ,Cognition in children -- Influence ,Biological sciences - Abstract
Study is conducted to show that low levels of Ras activity stimulate extracellular signal-regulated kinase kinase (MEK)-p42/44 MAPK (extracellular signal-regulated kinase B [ERK] signaling), whereas high levels of Ras activity stimulate additional Pi3 kinase (Pi3K)-protein kinase B (PKB) signaling. Ras-MEK-ERK activity in sleeping animals is sufficient to deliver GluR2L into synapses, while additional increased Ras-Pi3K-PKB activity in awaken animals delivers GluR1 synapses
- Published
- 2005
7. F196. Transgenic Overexpression of the Type III Isoform of Neuregulin 1 in Mice Induces Abnormalities on Auditory Event Related EEG Biomarkers Related to Schizophrenia Accompanied by Reduction of Parvalbumin Positive Interneurons in the Prefrontal Cortex
- Author
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Schuelert, Niklas, Nissen, Wiebke, Mack, Volker, Jaeger, Stefan, Arban, Roberto, Schwab, Markus, Rossner, Moritz, Dorner-Ciossek, Cornelia, and Rosenbrock, Holger
- Published
- 2018
- Full Text
- View/download PDF
8. Noelin1 Affects Lateral Mobility of Synaptic AMPA Receptors.
- Author
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Pandya, Nikhil J., Seeger, Christian, Babai, Norbert, Gonzalez-Lozano, Miguel A., Mack, Volker, Lodder, Johannes C., Gouwenberg, Yvonne, Mansvelder, Huibert D., Danielson, U. Helena, Li, Ka Wan, Heine, Martin, Spijker, Sabine, Frischknecht, Renato, and Smit, August B.
- Abstract
Summary Lateral diffusion on the neuronal plasma membrane of the AMPA-type glutamate receptor (AMPAR) serves an important role in synaptic plasticity. We investigated the role of the secreted glycoprotein Noelin1 (Olfactomedin-1 or Pancortin) in AMPAR lateral mobility and its dependence on the extracellular matrix (ECM). We found that Noelin1 interacts with the AMPAR with high affinity, however, without affecting rise- and decay time and desensitization properties. Noelin1 co-localizes with synaptic and extra-synaptic AMPARs and is expressed at synapses in an activity-dependent manner. Single-particle tracking shows that Noelin1 reduces lateral mobility of both synaptic and extra-synaptic GluA1-containing receptors and affects short-term plasticity. While the ECM does not constrain the synaptic pool of AMPARs and acts only extrasynaptically, Noelin1 contributes to synaptic potentiation by limiting AMPAR mobility at synaptic sites. This is the first evidence for the role of a secreted AMPAR-interacting protein on mobility of GluA1-containing receptors and synaptic plasticity. [ABSTRACT FROM AUTHOR]
- Published
- 2018
- Full Text
- View/download PDF
9. Characterization of HTT Inclusion Size, Location, and Timing in the zQ175 Mouse Model of Huntington´s Disease: An In Vivo High-Content Imaging Study.
- Author
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Carty, Nikisha, Berson, Nadège, Tillack, Karsten, Thiede, Christina, Scholz, Diana, Kottig, Karsten, Sedaghat, Yalda, Gabrysiak, Christina, Yohrling, George, von der Kammer, Heinz, Ebneth, Andreas, Mack, Volker, Munoz-Sanjuan, Ignacio, and Kwak, Seung
- Subjects
HUNTINGTON disease ,HUNTINGTIN protein ,NEURODEGENERATION ,TRINUCLEOTIDE repeats ,PROTEIN expression ,LABORATORY mice ,MEDICAL imaging systems - Abstract
Huntington’s disease (HD) is an autosomal dominant neurodegenerative disorder caused by a CAG trinucleotide repeat expansion in the huntingtin gene. Major pathological hallmarks of HD include inclusions of mutant huntingtin (mHTT) protein, loss of neurons predominantly in the caudate nucleus, and atrophy of multiple brain regions. However, the early sequence of histological events that manifest in region- and cell-specific manner has not been well characterized. Here we use a high-content histological approach to precisely monitor changes in HTT expression and characterize deposition dynamics of mHTT protein inclusion bodies in the recently characterized zQ175 knock-in mouse line. We carried out an automated multi-parameter quantitative analysis of individual cortical and striatal cells in tissue slices from mice aged 2–12 months and confirmed biochemical reports of an age-associated increase in mHTT inclusions in this model. We also found distinct regional and subregional dynamics for inclusion number, size and distribution with subcellular resolution. We used viral-mediated suppression of total HTT in the striatum of zQ175 mice as an example of a therapeutically-relevant but heterogeneously transducing strategy to demonstrate successful application of this platform to quantitatively assess target engagement and outcome on a cellular basis. [ABSTRACT FROM AUTHOR]
- Published
- 2015
- Full Text
- View/download PDF
10. The Structure of Mammalian Serine Racemase.
- Author
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Smith, Myron A., Mack, Volker, Ebneth, Andreas, Moraes, Isabel, Felicetti, Brunella, Wood, Michael, Schonfeld, Dorian, Mather, Owen, Cesura, Andrea, and Barker, John
- Subjects
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SERINE , *METHYL aspartate , *GLUTAMIC acid , *BINDING sites , *ENZYMES , *CATALYSTS - Abstract
Serine racemase is responsible for the synthesis of D-serine, an endogenous co-agonist for N-methyl-D-aspartate receptor-type glutamate receptors (NMDARs). This pyridoxal 5'-phosphate-dependent enzyme is involved both in the reversible conversion of L- to D-serine and serine catabolism by α,β-elimination of water, thereby regulating D-serine levels. Because D-serine affects NMDAR signaling throughout the brain, serine racemase is a promising target for the treatment of disorders related to NMDAR dysfunction. To provide a molecular basis for rational drug design the x-ray crystal structures of human and rat serine racemase were determined at 1.5- and 2.1-Å resolution, respectively, and in the presence and absence of the orthosteric inhibitor malonate. The structures revealed a fold typical of β-family pyridoxal 5'-phosphate enzymes, with both a large domain and a flexible small domain associated into a symmetric dimer, and indicated a ligand-induced rearrangement of the small domain that organizes the active site for specific turnover of the substrate. [ABSTRACT FROM AUTHOR]
- Published
- 2010
- Full Text
- View/download PDF
11. Enhanced Odor Discrimination and Impaired Olfactory Memory by Spatially Controlled Switch of AMPA Receptors.
- Author
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Shimshek, Derya R., Bus, Thorsten, Kim, Jinhyun, Mihaljevic, Andre, Mack, Volker, Seeburg, Peter H., Sprengel, Rolf, and Schaefer, Andreas T.
- Subjects
DRUG receptors ,CALCIUM ,CONDITIONED response ,SMELL ,SMELL disorders ,SENSES - Abstract
Genetic perturbations of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionate receptors (AMPARs) are widely used to dissect molecular mechanisms of sensory coding, learning, and memory. In this study, we investigated the role of Ca
2+ -permeable AMPARs in olfactory behavior. AMPAR modification was obtained by depletion of the GluR-B subunit or expression of unedited GluR-B(Q), both leading to increased Ca2+ permeability of AMPARs. Mice with this functional AMPAR switch, specifically in forebrain, showed enhanced olfactory discrimination and more rapid learning in a go/no-go operant conditioning task. Olfactory memory, however, was dramatically impaired. GluR-B depletion in forebrain was ectopically variable ("mosaic") among individuals and strongly correlated with decreased olfactory memory in hippocampus and cortex. Accordingly, memory was rescued by transgenic GluR-B expression restricted to piriform cortex and hippocampus, while enhanced odor discrimination was independent of both GluR-B variability and transgenic GluR-B expression. Thus, correlated differences in behavior and levels of GluR-B expression allowed a mechanistic and spatial dissection of olfactory learning, discrimination, and memory capabilities. [ABSTRACT FROM AUTHOR]- Published
- 2005
- Full Text
- View/download PDF
12. DEVELOPMENTAL PROGRESSION OF INTERNEURON NETWORK DEFICITS IN A 15Q13.3 MICRODELETION MOUSE MODEL – A GLIMPSE ON ADOLESCENT PRIMING FOR SCHIZOPHRENIA?
- Author
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Funk, Marzieh, Jaeger, Stefan, Schülert, Niklas, Dorner-Ciossek, Cornelia, Rosenbrock, Holger, and Mack, Volker
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BIOLOGICAL models ,CEREBRAL cortex ,CONFERENCES & conventions ,NEURONS ,NEUROPLASTICITY ,SCHIZOPHRENIA - Abstract
Background: Schizophrenia is a complex neurodevelopmental disorder. Patients typically start exhibiting symptoms during adolescence, coinciding with a critical period for the maturation of the prefrontal cortex. While previous studies have identified deficits in cortical interneuron integrity and network function in chronic patients, little is known about the maladaptive circuitry in the early prodromal phase of the disease. To assess pathophysiological changes during adolescence that might contribute to the disruption of cortical network function we have studied a 15q13.3 microdeletion mouse model Df[h15q13]−/+ resembling a human copy number variant (CNV) known to confer high risk for psychiatric disorders such as schizophrenia. Using a combination of histology, in vitro electrophysiology and electroencephalography (EEG) we explored the interneuronal connectivity and cortical network functionality in the Df[h15q13]−/+ mouse model from adolescence to early adulthood Methods: Immunohistological analysis was performed on brain slices within the prefrontal cortex, dorsal hippocampus and amygdala region from Df[h15q13]−/+ and wild-type mice (N=8) at PND35 and PND70 (4 sections/brain). Sections were immunostained for markers of interneuron subtypes and respective synapses. Fluorescence images were recorded and processed with an Opera Phenix (PerkinElmer) using the 63x objective in confocal mode. EEG studies were performed on Df[h15q13]−/+ and wild-type mice within the age range of PND41 to PND70 (6). Mice were obtained from Taconic and housed within the experimental facility for at least one week prior to experimental procedures. Results: We initially confirmed that the adult Df[h15q13]−/+ microdeletion mouse model exhibits robust markers reminiscent of schizophrenialinked pathology, such as the reduction of parvalbumin positive (PV+) interneurons, lower abundance of perineuronal net proteins (PNNs) and an impaired cortical processing of sensory information. We identified abnormalities in the number and distribution of interneuron synapses in the prefrontal cortex, hippocampus and amygdala, the phenotype in the adolescent brain, which were opposed to pathophysiological changes identified in adult Df[h15q13]−/+ microdeletion mice. We discovered an enhanced inhibitory drive from specific subpopulations of interneurons during adolescence that might contribute to deficits in the adult hippocampal and PFC network. Likewise, we found Df[h15q13]−/+ specific differences in cortical network processing between adolescent and adult mice revealed by EEG. To align the development of cortical network function to the progressive changes in network structure we performed longitudinal EEG recordings and uncovered particular abnormalities in basal and evoked oscillatory rhythms in adolescent and adult mice. Discussion: In this study, we discovered abnormalities in the interneuron integration during a critical period for the maturation of the prefrontal cortex in a 15q13.3 microdeletion mouse model. Our findings provide novel insights into early deficits in the limbic and cortical neuronal networks that may drive circuit dysfunction in schizophrenia patients. Identification of adolescent pathophysiology in models for schizophrenia risk will provide the opportunity to explore new mechanisms for early intervention. [ABSTRACT FROM AUTHOR]
- Published
- 2020
- Full Text
- View/download PDF
13. Neural adaption in midbrain GABAergic cells contributes to high-fat diet-induced obesity.
- Author
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Xiaomeng Wang, Xiaotong Wu, Hao Wu, Hanyang Xiao, Sijia Hao, Bingwei Wang, Chen Li, Bleymehl, Katherin, Kauschke, Stefan G., Mack, Volker, Ferger, Boris, Klein, Holger, Ruimao Zheng, Shumin Duan, and Hao Wang
- Subjects
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WHITE adipose tissue , *MESENCEPHALON , *OBESITY , *GENE expression , *FAT , *RNA sequencing - Abstract
Overeating disorders largely contribute to worldwide incidences of obesity. Available treatments are limited. Here, we discovered that long-term chemogenetic activation of ventrolateral periaqueductal gray (vlPAG) GABAergic cells rescue obesity of high-fat diet-induced obesity (DIO) mice. Thiswas associated with the recovery of enhanced mIPSCs, decreased food intake, increased energy expenditure, and inguinal white adipose tissue (iWAT) browning. In vivo calcium imaging confirmed vlPAG GABAergic suppression for DIO mice, with corresponding reduction in intrinsic excitability. Single-nucleus RNA sequencing identified transcriptional expression changes in GABAergic cell subtypes in DIO mice, highlighting Cacna2d1 as of potential importance. Overexpressing CACNA2D1 in vlPAG GABAergic cells of DIO mice rescued enhanced mIPSCs and calcium response, reversed obesity, and therefore presented here as a potential target for obesity treatment. [ABSTRACT FROM AUTHOR]
- Published
- 2023
- Full Text
- View/download PDF
14. Forebrain-Specific Glutamate Receptor B Deletion Impairs Spatial Memory But Not Hippocampal Field Long-Term Potentiation.
- Author
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Shimshek, Derya R., Jensen, Vidar, Celikel, Tansu, Yu Geng, Schupp, Bettina, Bus, Thorsten, Mack, Volker, Marx, Verena, Hvalby, Øivind, Seeburg, Peter H., and Sprengel, Rolf
- Subjects
HIPPOCAMPUS (Brain) ,LABORATORY mice ,PROSENCEPHALON ,NEURONS ,DEVELOPMENTAL neurobiology - Abstract
We demonstrate the fundamental importance of glutamate receptor B (GluR-B) containing AMPA receptors in hippocampal function by analyzing mice with conditional GluR-B deficiency in postnatal forebrain principal neurons (GluR-B
ΔFb ). These mice are as adults sufficiently robust to permit comparative cellular, physiological, and behavioral studies. GluR-B loss induced moderate long-term changes in the hippocampus of GluR-BΔFb mice. Parvalbumin-expressing interneurons in the dentate gyrus and the pyramidal cells in CA3 were decreased in number, and neurogenesis in the subgranular zone was diminished. Excitatory synaptic CA3-to-CA1 transmission was reduced, although synaptic excitability, as quantified by the lowered threshold for population spike initiation, was increased compared with control mice. These changes did not alter CA3-to-CA1 long-term potentiation (LTP), which in magnitude was similar to LTP in control mice. The altered hippocampal circuitry, however, affected spatial learning in GluR-BΔFb mice. The primary source for the observed changes is most likely the AMPA receptor-mediated Ca2+ signaling that appears after GluR-B depletion, because we observed similar alterations in GluR-BΔFb mice in which the expression of Ca2+ -permeable AMPA receptors in principal neurons was induced by postnatal activation of a Q/R-site editing-deficient GluR-B allele. [ABSTRACT FROM AUTHOR]- Published
- 2006
- Full Text
- View/download PDF
15. Increasing the Excitatory Drive Rescues Excitatory/Inhibitory Imbalance and Mismatch Negativity Deficit Caused by Parvalbumin Specific GluA1 Deletion.
- Author
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Chen-Engerer, Hsing-Jung, Jaeger, Stefan, Bondarenko, Rimma, Sprengel, Rolf, Hengerer, Bastian, Rosenbrock, Holger, Mack, Volker, and Schuelert, Niklas
- Subjects
- *
NEURAL circuitry , *PYRAMIDAL neurons , *PREFRONTAL cortex , *AMPA receptors , *SENSORIMOTOR integration - Abstract
[Display omitted] • We offer a systematic workflow to study how GlyT1 inhibitor restores E/I imbalance-mediated cortical network dysfunction. • PV-specific GluA1 knock-out is an ideal experimental tool to study E/I imbalance-caused cortical network abnormality. • Boosting NMDA receptor-related signaling pathway restores E/I imbalance-mediated mismatch negativity deficit. Disturbance in synaptic excitatory and inhibitory (E/I) transmission in the prefrontal cortex is considered a critical factor for cognitive dysfunction, a core symptom in schizophrenia. However, the cortical network pathophysiology induced by E/I imbalance is not well characterized, and an effective therapeutic strategy is lacking. In this study, we simulated imbalanced cortical network by using mice with parvalbumin neuron (PV) specific knockout of GluA1 (AMPA receptor subunit 1) (Gria1-PV KO) as an experimental model. Applying high-content confocal imaging and electrophysiological recordings in the medial prefrontal cortex (mPFC), we found structural and functional alterations in the local network of Gria1-PV KO mice. Additionally, we applied electroencephalography (EEG) to assess potential deficits in mismatch negativity (MMN), the standard readout in the clinic for measuring deviance detection and sensory information processing. Gria1-PV KO animals exhibited abnormal theta oscillation and MMN, which is consistent with clinical findings in cognitively impaired patients. Remarkably, we demonstrated that the glycine transporter 1 (GlyT1) inhibitor, Bitopertin, ameliorates E/I imbalance, hyperexcitability, and sensory processing malfunction in Gria1-PV KO mice. Our results suggest that PV-specific deletion of GluA1 might be an experimental approach for back translating the E/I imbalance observed in schizophrenic patients. Our work offers a systematic workflow to understand the effect of GlyT1 inhibition in restoring cortical network activity from single cells to local brain circuitry. This study highlights that selectively boosting NMDA receptor-mediated excitatory drive to enhance the network inhibitory transmission from interneurons to pyramidal neurons (PYs) is a potential therapeutic strategy for restoring E/I imbalance-associated cognitive-related abnormality. [ABSTRACT FROM AUTHOR]
- Published
- 2022
- Full Text
- View/download PDF
16. GluA1 and its PDZ-interaction: A role in experience-dependent behavioral plasticity in the forced swim test
- Author
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Freudenberg, Florian, Marx, Verena, Mack, Volker, Layer, Liliana E., Klugmann, Matthias, Seeburg, Peter H., Sprengel, Rolf, and Celikel, Tansu
- Subjects
- *
GLUTAMATE receptors , *PROTEIN-protein interactions , *NEUROPLASTICITY , *MENTAL depression , *BEHAVIORAL assessment , *DESPAIR -- Testing , *MESSENGER RNA - Abstract
Abstract: Glutamate receptor dependent synaptic plasticity plays an important role in the pathophysiology of depression. Hippocampal samples from clinically depressed patients display reduced mRNA levels for GluA1, a major subunit of AMPA receptors. Moreover, activation and synaptic incorporation of GluA1-containing AMPA receptors are required for the antidepressant-like effects of NMDA receptor antagonists. These findings argue that GluA1-dependent synaptic plasticity might be critically involved in the expression of depression. Using an animal model of depression, we demonstrate that global or hippocampus-selective deletion of GluA1 impairs expression of experience-dependent behavioral despair. This impairment is mediated by the interaction of GluA1 with PDZ-binding domain proteins, as deletion of the C-terminal leucine alone is sufficient to replicate the behavioral phenotype. Our results provide evidence for a significant role of hippocampal GluA1-containing AMPA receptors and their PDZ-interaction in experience-dependent expression of behavioral despair and link mechanisms of hippocampal synaptic plasticity with behavioral expression of depression. [Copyright &y& Elsevier]
- Published
- 2013
- Full Text
- View/download PDF
17. Differential GABAA receptor clustering determines GABA synapse plasticity in rat oxytocin neurons around parturition and the onset of lactation
- Author
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Koksma, Jan-Jurjen, Fritschy, Jean-Marc, Mack, Volker, Van Kesteren, Ronald E., and Brussaard, Arjen B.
- Subjects
- *
GABA , *PARTURITION , *SYNAPSES , *NEURONS - Abstract
Abstract: Expression, functional properties, and clustering of α1-, α2-, and α3-subunit containing GABAA receptors (GABAARs) were studied in dorsomedial SON neurons of the adult female rat supraoptic nucleus (SON) around parturition. We show that, although the decay time constant (τdecay) of GABAergic postsynaptic currents between and within individual recordings was very diverse, ranging from fast (i.e., α1-like) to significantly slower (i.e., non-α1-like), there was an overall shift towards slower decaying synaptic currents during the onset of lactation. This shift is not due to changes in mRNA expression levels, because real-time quantitative PCR assays indicated that the relative contribution of α1, α2, and α3 remained the same before and after parturition. Also, changes in phosphorylation levels are not likely to affect the τdecay of postsynaptic currents. In α-latrotoxin (α-LTX)-induced bursts of synaptic currents from individual synapses, the τdecay of consecutive synaptic events within bursts was very similar, but between bursts there were large differences in τdecay. This suggested that different synapses within individual SON neurons contain distinct GABAAR subtypes. Using multilabeling confocal microscopy, we examined the distribution of postsynaptic α1-, α2-, and α3-GABAARs, based on colocalization with gephyrin. We show that the three GABAAR subtypes occurred either in segregated clusters of one subtype as well as in mixed clusters of two or possibly even three receptor subtypes. After parturition, the density and proportion of clusters containing α2- (or α3-), but not α1-GABAARs, was significantly increased. Thus, the functional synaptic diversity at the postsynaptic level in dorsomedial SON neurons is correlated with a differential clustering of distinct GABAAR subtypes at individual synapses. [Copyright &y& Elsevier]
- Published
- 2005
- Full Text
- View/download PDF
18. Glutamatergic Plasticity by Synaptic Delivery of GluR-Blong-Containing AMPA Receptors
- Author
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Kolleker, Alexander, Zhu, J. Julius, Schupp, Bettina J., Qin, Yi, Mack, Volker, Borchardt, Thilo, Köhr, Georg, Malinow, Roberto, Seeburg, Peter H., and Osten, Pavel
- Subjects
- *
NEUROPLASTICITY , *HIPPOCAMPUS (Brain) , *LEARNING , *NEURONS - Abstract
Activity-driven delivery of AMPA receptors is proposed to mediate glutamatergic synaptic plasticity, both during development and learning. In hippocampal CA1 principal neurons, such trafficking is primarily mediated by the abundant GluR-A subunit. We now report a study of GluR-Blong, a C-terminal splice variant of the GluR-B subunit. GluR-Blong synaptic delivery is regulated by two forms of activity. Spontaneous synaptic activity-driven GluR-Blong transport maintains one-third of the steady-state AMPA receptor-mediated responses, while GluR-Blong delivery following the induction of LTP is responsible for approximately 50% of the resulting potentiation at the hippocampal CA3 to CA1 synapses at the time of GluR-Blong peak expression—the second postnatal week. Trafficking of GluR-Blong-containing receptors thus mediates a GluR-A-independent form of glutamatergic synaptic plasticity in the juvenile hippocampus. [Copyright &y& Elsevier]
- Published
- 2003
- Full Text
- View/download PDF
19. Neural adaption in midbrain GABAergic cells contributes to high-fat diet-induced obesity.
- Author
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Wang X, Wu X, Wu H, Xiao H, Hao S, Wang B, Li C, Bleymehl K, Kauschke SG, Mack V, Ferger B, Klein H, Zheng R, Duan S, and Wang H
- Subjects
- Mice, Animals, Obesity etiology, Obesity metabolism, Adipose Tissue, White metabolism, Mesencephalon, Mice, Inbred C57BL, Diet, High-Fat adverse effects, Calcium metabolism
- Abstract
Overeating disorders largely contribute to worldwide incidences of obesity. Available treatments are limited. Here, we discovered that long-term chemogenetic activation of ventrolateral periaqueductal gray (vlPAG) GABAergic cells rescue obesity of high-fat diet-induced obesity (DIO) mice. This was associated with the recovery of enhanced mIPSCs, decreased food intake, increased energy expenditure, and inguinal white adipose tissue (iWAT) browning. In vivo calcium imaging confirmed vlPAG GABAergic suppression for DIO mice, with corresponding reduction in intrinsic excitability. Single-nucleus RNA sequencing identified transcriptional expression changes in GABAergic cell subtypes in DIO mice, highlighting Cacna2d1 as of potential importance. Overexpressing CACNA2D1 in vlPAG GABAergic cells of DIO mice rescued enhanced mIPSCs and calcium response, reversed obesity, and therefore presented here as a potential target for obesity treatment.
- Published
- 2023
- Full Text
- View/download PDF
20. Allosteric Activation of Striatal-Enriched Protein Tyrosine Phosphatase (STEP, PTPN5) by a Fragment-like Molecule.
- Author
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Tautermann CS, Binder F, Büttner FH, Eickmeier C, Fiegen D, Gross U, Grundl MA, Heilker R, Hobson S, Hoerer S, Luippold A, Mack V, Montel F, Peters S, Bhattacharya S, Vaidehi N, Schnapp G, Thamm S, and Zeeb M
- Subjects
- Allosteric Regulation, Allosteric Site, Animals, Catalytic Domain, Crystallography, X-Ray, Enzyme Inhibitors chemistry, Enzyme Inhibitors metabolism, Humans, Mice, Molecular Dynamics Simulation, Nuclear Magnetic Resonance, Biomolecular, Protein Binding, Protein Isoforms chemistry, Protein Isoforms metabolism, Protein Tyrosine Phosphatases, Non-Receptor metabolism, Small Molecule Libraries metabolism, Protein Tyrosine Phosphatases, Non-Receptor chemistry, Small Molecule Libraries chemistry
- Abstract
Protein tyrosine phosphatase non-receptor type 5 (PTPN5, STEP) is a brain specific phosphatase that regulates synaptic function and plasticity by modulation of N-methyl-d-aspartate receptor (NMDAR) and α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor (AMPAR) trafficking. Dysregulation of STEP has been linked to neurodegenerative and neuropsychiatric diseases, highlighting this enzyme as an attractive therapeutic target for drug discovery. Selective targeting of STEP with small molecules has been hampered by high conservation of the active site among protein tyrosine phosphatases. We report the discovery of the first small molecule allosteric activator for STEP that binds to the phosphatase domain. Allosteric binding is confirmed by both X-ray and
15 N NMR experiments, and specificity has been demonstrated by an enzymatic test cascade. Molecular dynamics simulations indicate stimulation of enzymatic activity by a long-range allosteric mechanism. To allow the scientific community to make use of this tool, we offer to provide the compound in the course of an open innovation initiative.- Published
- 2019
- Full Text
- View/download PDF
21. State-dependent Ras signaling and AMPA receptor trafficking.
- Author
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Qin Y, Zhu Y, Baumgart JP, Stornetta RL, Seidenman K, Mack V, van Aelst L, and Zhu JJ
- Subjects
- Animals, Hippocampus drug effects, Hippocampus metabolism, Histamine pharmacology, In Vitro Techniques, Long-Term Potentiation, MAP Kinase Signaling System, Models, Neurological, Mutagenesis, Site-Directed, Neuronal Plasticity, Neurotransmitter Agents pharmacology, Phosphatidylinositol 3-Kinases metabolism, Phosphorylation, Protein Serine-Threonine Kinases metabolism, Proto-Oncogene Proteins metabolism, Proto-Oncogene Proteins c-akt, Rats, Receptors, AMPA genetics, Recombinant Fusion Proteins genetics, Recombinant Fusion Proteins metabolism, Signal Transduction, Synapses metabolism, ras Proteins genetics, Receptors, AMPA metabolism, ras Proteins metabolism
- Abstract
Synaptic trafficking of AMPA-Rs, controlled by small GTPase Ras signaling, plays a key role in synaptic plasticity. However, how Ras signals synaptic AMPA-R trafficking is unknown. Here we show that low levels of Ras activity stimulate extracellular signal-regulated kinase kinase (MEK)-p42/44 MAPK (extracellular signal-regulated kinase [ERK]) signaling, whereas high levels of Ras activity stimulate additional Pi3 kinase (Pi3K)-protein kinase B (PKB) signaling, each accounting for approximately 50% of the potentiation during long-term potentiation (LTP). Spontaneous neural activity stimulates the Ras-MEK-ERK pathway that drives GluR2L into synapses. In the presence of neuromodulator agonists, neural activity also stimulates the Ras-Pi3K-PKB pathway that drives GluR1 into synapses. Neuromodulator release increases with increases of vigilance. Correspondingly, Ras-MEK-ERK activity in sleeping animals is sufficient to deliver GluR2L into synapses, while additional increased Ras-Pi3K-PKB activity in awake animals delivers GluR1 into synapses. Thus, state-dependent Ras signaling, which specifies downstream MEK-ERK and Pi3K-PKB pathways, differentially control GluR2L- and GluR1-dependent synaptic plasticity.
- Published
- 2005
- Full Text
- View/download PDF
22. Glutamatergic plasticity by synaptic delivery of GluR-B(long)-containing AMPA receptors.
- Author
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Kolleker A, Zhu JJ, Schupp BJ, Qin Y, Mack V, Borchardt T, Köhr G, Malinow R, Seeburg PH, and Osten P
- Subjects
- Amino Acid Sequence, Animals, Mice, Mice, Inbred C57BL, Mice, Knockout, Molecular Sequence Data, Neuronal Plasticity physiology, Protein Transport physiology, Receptors, AMPA biosynthesis, Receptors, AMPA genetics, Sequence Analysis, Protein methods, Synapses genetics, Receptors, AMPA deficiency, Synapses metabolism
- Abstract
Activity-driven delivery of AMPA receptors is proposed to mediate glutamatergic synaptic plasticity, both during development and learning. In hippocampal CA1 principal neurons, such trafficking is primarily mediated by the abundant GluR-A subunit. We now report a study of GluR-B(long), a C-terminal splice variant of the GluR-B subunit. GluR-B(long) synaptic delivery is regulated by two forms of activity. Spontaneous synaptic activity-driven GluR-B(long) transport maintains one-third of the steady-state AMPA receptor-mediated responses, while GluR-B(long) delivery following the induction of LTP is responsible for approximately 50% of the resulting potentiation at the hippocampal CA3 to CA1 synapses at the time of GluR-B(long) peak expression-the second postnatal week. Trafficking of GluR-B(long)-containing receptors thus mediates a GluR-A-independent form of glutamatergic synaptic plasticity in the juvenile hippocampus.
- Published
- 2003
- Full Text
- View/download PDF
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