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  1. Article ; Online: Comparative study for the IMI2-NeuroDeRisk project on microelectrode arrays to derisk drug-induced seizure liability.

    Zhai, Jin / Traebert, Martin / Zimmermann, Kurt / Delaunois, Annie / Royer, Leandro / Salvagiotto, Giorgia / Carlson, Coby / Lagrutta, Armando

    Journal of pharmacological and toxicological methods

    2023  Volume 123, Page(s) 107297

    Abstract: Introduction: In the framework of the IMI2-NeuroDeRisk consortium, three in vitro electrophysiology assays were compared to improve preclinical prediction of seizure-inducing liabilities.: Methods: Two cell models, primary rat cortical neurons and ... ...

    Abstract Introduction: In the framework of the IMI2-NeuroDeRisk consortium, three in vitro electrophysiology assays were compared to improve preclinical prediction of seizure-inducing liabilities.
    Methods: Two cell models, primary rat cortical neurons and human induced pluripotent stem cell (hiPSC)-derived glutamatergic neurons co-cultured with hiPSC-derived astrocytes were tested on two different microelectrode array (MEA) platforms, Maestro Pro (Axion Biosystems) and Multiwell-MEA-System (Multi Channel Systems), in three separate laboratories. Pentylenetetrazole (PTZ) and/or picrotoxin (PTX) were included in each plate as positive (n = 3-6 wells) and ≤0.2% DMSO was used as negative controls (n = 3-12 wells). In general, concentrations in a range of 0.1-30 μM were tested, anchored, when possible, on clinically relevant exposures (unbound C
    Results: Neuronal activity of 33 compounds categorized as positive tool drugs, seizure-positive or seizure-negative compounds was evaluated. Acute drug effects (<60 min) were compared to baseline recordings. Time points < 15 min exhibited stronger, less variable responses to many of the test agents. For many compounds a reduction and cessation of neuronal activity was detected at higher test concentrations. There was not a single pattern of seizurogenic activity detected, even among tool compounds, likely due to different mechanisms of actions and/or off-target profiles. A post-hoc analysis focusing on changes indicative of neuronal excitation is presented.
    Conclusion: All cell models showed good sensitivity, ranging from 70 to 86%. Specificity ranged from 40 to 70%. Compared to more conventional measurements of evoked activity in hippocampal slices, these plate-based models provide higher throughput and the potential to study subacute responses. Yet, they may be limited by the random, spontaneous nature of their network activity.
    MeSH term(s) Rats ; Humans ; Animals ; Microelectrodes ; Cells, Cultured ; Induced Pluripotent Stem Cells ; Seizures/chemically induced ; Neurons
    Language English
    Publishing date 2023-07-25
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1105919-9
    ISSN 1873-488X ; 1056-8719
    ISSN (online) 1873-488X
    ISSN 1056-8719
    DOI 10.1016/j.vascn.2023.107297
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  2. Article ; Online: Comparative study for the IMI2-NeuroDeRisk project on microelectrode arrays to derisk drug-induced seizure liability

    Zhai, Jin / Traebert, Martin / Zimmermann, Kurt / Delaunois, Annie / Royer, Leandro / Salvagiotto, Giorgia / Carlson, Coby / Lagrutta, Armando

    Journal of Pharmacological and Toxicological Methods. 2023 July 25, p.107297-

    2023  , Page(s) 107297–

    Abstract: In the framework of the IMI2-NeuroDeRisk consortium, three in vitro electrophysiology assays were compared to improve preclinical prediction of seizure-inducing liabilities. Two cell models, primary rat cortical neurons and human induced pluripotent stem ...

    Abstract In the framework of the IMI2-NeuroDeRisk consortium, three in vitro electrophysiology assays were compared to improve preclinical prediction of seizure-inducing liabilities. Two cell models, primary rat cortical neurons and human induced pluripotent stem cell (hiPSC)-derived glutamatergic neurons co-cultured with hiPSC-derived astrocytes were tested on two different microelectrode array (MEA) platforms, Maestro Pro (Axion Biosystems) and Multiwell-MEA-System (Multi Channel Systems), in three separate laboratories. Pentylenetetrazole (PTZ) and/or picrotoxin (PTX) were included in each plate as positive (n = 3–6 wells) and ≤0.2% DMSO was used as negative controls (n = 3–12 wells). In general, concentrations in a range of 0.1–30 μM were tested, anchored, when possible, on clinically relevant exposures (unbound Cₘₐₓ) were tested. Activity thresholds for drug-induced changes were set at 20%. To evaluate sensitivity, specificity and predictivity of the cell models, seizurogenic responses were defined as changes in 4 or more endpoints. Concentration dependence trends were also considered. Neuronal activity of 33 compounds categorized as positive tool drugs, seizure-positive or seizure-negative compounds was evaluated. Acute drug effects (<60 min) were compared to baseline recordings. Time points < 15 min exhibited stronger, less variable responses to many of the test agents. For many compounds a reduction and cessation of neuronal activity was detected at higher test concentrations. There was not a single pattern of seizurogenic activity detected, even among tool compounds, likely due to different mechanisms of actions and/or off-target profiles. A post-hoc analysis focusing on changes indicative of neuronal excitation is presented. All cell models showed good sensitivity, ranging from 70 to 86%. Specificity ranged from 40 to 70%. Compared to more conventional measurements of evoked activity in hippocampal slices, these plate-based models provide higher throughput and the potential to study subacute responses. Yet, they may be limited by the random, spontaneous nature of their network activity.
    Keywords astrocytes ; coculture ; comparative study ; drugs ; electrophysiology ; humans ; neurons ; prediction ; rats ; stem cells ; toxicology ; Cortical neurons ; hiPSC ; In vitro ; MEA ; Methods ; Neurotoxicity ; Rat ; Safety pharmacology ; Seizures ; 4-AP ; AMIT ; ASC ; AXPN ; AZE ; BIC ; BUP ; CPZ ; CLZ ; CNS ; DFN ; DMSO ; DPH ; DON ; FN ; FAERS ; FAERS+ ; FAERS- ; FP ; GNC ; IMQ ; INH ; KA ; MPT ; MCZ ; MNX ; MIR ; NPV ; NIA ; OSP ; PRX ; PTX ; PILO ; PEI ; PPV ; PTZ ; ROF ; RSG ; SD ; STRY ; TMZ ; TPH ; TRA ; TN ; TP ; VLB ; VEN
    Language English
    Dates of publication 2023-0725
    Publishing place Elsevier Inc.
    Document type Article ; Online
    Note Pre-press version
    ZDB-ID 1105919-9
    ISSN 1873-488X ; 1056-8719
    ISSN (online) 1873-488X
    ISSN 1056-8719
    DOI 10.1016/j.vascn.2023.107297
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  3. Article ; Online: GABA

    Bampali, Konstantina / Koniuszewski, Filip / Vogel, Florian D / Fabjan, Jure / Andronis, Christos / Lekka, Eftychia / Virvillis, Vassilis / Seidel, Thomas / Delaunois, Annie / Royer, Leandro / Rolf, Michael G / Giuliano, Chiara / Traebert, Martin / Roussignol, Gautier / Fric-Bordat, Magali / Mazelin-Winum, Ludmilla / Bryant, Sharon D / Langer, Thierry / Ernst, Margot

    Cell biology and toxicology

    2023  Volume 39, Issue 6, Page(s) 2793–2819

    Abstract: ... ...

    Abstract GABA
    MeSH term(s) Animals ; Receptors, GABA-A/chemistry ; Receptors, GABA-A/metabolism ; Zebrafish ; Seizures/chemically induced ; Binding Sites ; gamma-Aminobutyric Acid
    Chemical Substances Receptors, GABA-A ; gamma-Aminobutyric Acid (56-12-2)
    Language English
    Publishing date 2023-04-24
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 48824-0
    ISSN 1573-6822 ; 0742-2091
    ISSN (online) 1573-6822
    ISSN 0742-2091
    DOI 10.1007/s10565-023-09803-y
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  4. Article: The Metastasis Suppressor Protein Nme1 Is a Concentration-Dependent Modulator of Ca2+/Calmodulin-Dependent Protein Kinase II

    Royer, Leandro / Shangraw, Kathryn / Herzog, Josiah J / Pouvreau, Sandrine / Marr, Michael T / Paradis, Suzanne

    Biochemistry. 2019 May 29, v. 58, no. 24

    2019  

    Abstract: Nucleoside diphosphate kinases (Nmes or NDPKs) have been implicated in a multitude of cellular processes, including an important role in metastasis suppression, and several enzymatic activities have been assigned to the Nme family. Nevertheless, for many ...

    Abstract Nucleoside diphosphate kinases (Nmes or NDPKs) have been implicated in a multitude of cellular processes, including an important role in metastasis suppression, and several enzymatic activities have been assigned to the Nme family. Nevertheless, for many of these processes, it has not been possible to establish a strong connection between Nme enzymatic activity and the relevant biological function. We hypothesized that, in addition to its known enzymatic functions, members of the Nme family might also regulate signaling cascades by acting on key signal transducers. Accordingly, here we show that Nme1 directly interacts with the calcium/calmodulin-dependent kinase II (CaMKII). Using purified proteins, we monitored the phosphorylation of a number of CaMKII substrates and determined that at nanomolar levels Nme1 enhances the phosphorylation of T-type substrates; this modulation shifts to inhibition at low micromolar concentrations. Specifically, the autophosphorylation of CaMKII at Thr286 is completely inhibited by 2 μM Nme1, a feature that distinguishes Nme1 from other known endogenous CaMKII inhibitors. Importantly, CaMKII inhibition does not require phosphotransfer activity by Nme1 because the kinase-dead Nme1 H118F mutant is as effective as the wild-type form of the enzyme. Our results provide a novel molecular mechanism whereby Nme1 could modulate diverse cellular processes in a manner that is independent of its known enzymatic activities.
    Keywords calcium-calmodulin-dependent protein kinase ; enzyme activity ; metastasis ; mutants ; nucleosides ; protein phosphorylation ; proteins ; signal transduction
    Language English
    Dates of publication 2019-0529
    Size p. 2710-2714.
    Publishing place American Chemical Society
    Document type Article
    ZDB-ID 1108-3
    ISSN 1520-4995 ; 0006-2960
    ISSN (online) 1520-4995
    ISSN 0006-2960
    DOI 10.1021/acs.biochem.9b00121
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  5. Article ; Online: The Metastasis Suppressor Protein Nme1 Is a Concentration-Dependent Modulator of Ca

    Royer, Leandro / Shangraw, Kathryn / Herzog, Josiah J / Pouvreau, Sandrine / Marr, Michael T / Paradis, Suzanne

    Biochemistry

    2019  Volume 58, Issue 24, Page(s) 2710–2714

    Abstract: Nucleoside diphosphate kinases (Nmes or NDPKs) have been implicated in a multitude of cellular processes, including an important role in metastasis suppression, and several enzymatic activities have been assigned to the Nme family. Nevertheless, for many ...

    Abstract Nucleoside diphosphate kinases (Nmes or NDPKs) have been implicated in a multitude of cellular processes, including an important role in metastasis suppression, and several enzymatic activities have been assigned to the Nme family. Nevertheless, for many of these processes, it has not been possible to establish a strong connection between Nme enzymatic activity and the relevant biological function. We hypothesized that, in addition to its known enzymatic functions, members of the Nme family might also regulate signaling cascades by acting on key signal transducers. Accordingly, here we show that Nme1 directly interacts with the calcium/calmodulin-dependent kinase II (CaMKII). Using purified proteins, we monitored the phosphorylation of a number of CaMKII substrates and determined that at nanomolar levels Nme1 enhances the phosphorylation of T-type substrates; this modulation shifts to inhibition at low micromolar concentrations. Specifically, the autophosphorylation of CaMKII at Thr286 is completely inhibited by 2 μM Nme1, a feature that distinguishes Nme1 from other known endogenous CaMKII inhibitors. Importantly, CaMKII inhibition does not require phosphotransfer activity by Nme1 because the kinase-dead Nme1 H118F mutant is as effective as the wild-type form of the enzyme. Our results provide a novel molecular mechanism whereby Nme1 could modulate diverse cellular processes in a manner that is independent of its known enzymatic activities.
    MeSH term(s) Animals ; Calcium-Calmodulin-Dependent Protein Kinase Type 2/antagonists & inhibitors ; Calcium-Calmodulin-Dependent Protein Kinase Type 2/chemistry ; Calcium-Calmodulin-Dependent Protein Kinase Type 2/metabolism ; Enzyme Assays ; Mice ; Mutation ; NM23 Nucleoside Diphosphate Kinases/chemistry ; NM23 Nucleoside Diphosphate Kinases/genetics ; NM23 Nucleoside Diphosphate Kinases/metabolism ; Protein Binding ; Tumor Suppressor Proteins/chemistry ; Tumor Suppressor Proteins/genetics ; Tumor Suppressor Proteins/metabolism
    Chemical Substances NM23 Nucleoside Diphosphate Kinases ; Tumor Suppressor Proteins ; Calcium-Calmodulin-Dependent Protein Kinase Type 2 (EC 2.7.11.17) ; Nme1 protein, mouse (EC 2.7.4.6)
    Language English
    Publishing date 2019-06-04
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 1108-3
    ISSN 1520-4995 ; 0006-2960
    ISSN (online) 1520-4995
    ISSN 0006-2960
    DOI 10.1021/acs.biochem.9b00121
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  6. Article ; Online: Rem2 signaling affects neuronal structure and function in part by regulation of gene expression.

    Kenny, Katelyn / Royer, Leandro / Moore, Anna R / Chen, Xiao / Marr, Michael T / Paradis, Suzanne

    Molecular and cellular neurosciences

    2017  Volume 85, Page(s) 190–201

    Abstract: The central nervous system has the remarkable ability to convert changes in the environment in the form of sensory experience into long-term alterations in synaptic connections and dendritic arborization, in part through changes in gene expression. ... ...

    Abstract The central nervous system has the remarkable ability to convert changes in the environment in the form of sensory experience into long-term alterations in synaptic connections and dendritic arborization, in part through changes in gene expression. Surprisingly, the molecular mechanisms that translate neuronal activity into changes in neuronal connectivity and morphology remain elusive. Rem2, a member of the Rad/Rem/Rem2/Gem/Kir (RGK) subfamily of small Ras-like GTPases, is a positive regulator of synapse formation and negative regulator of dendritic arborization. Here we identify that one output of Rem2 signaling is the regulation of gene expression. Specifically, we demonstrate that Rem2 signaling modulates the expression of genes required for a variety of cellular processes from neurite extension to synapse formation and synaptic function. Our results highlight Rem2 as a unique molecule that transduces changes in neuronal activity detected at the cell membrane to morphologically relevant changes in gene expression in the nucleus.
    MeSH term(s) Animals ; Brain/embryology ; Brain/metabolism ; Cells, Cultured ; Gene Expression Regulation/physiology ; Gene Knockout Techniques ; Mice ; Monomeric GTP-Binding Proteins/metabolism ; Neurogenesis/physiology ; Neurons/cytology ; Neurons/metabolism ; Signal Transduction/physiology
    Chemical Substances Monomeric GTP-Binding Proteins (EC 3.6.5.2) ; Rem2 protein, mouse (EC 3.6.5.2)
    Language English
    Publishing date 2017-10-21
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 1046640-x
    ISSN 1095-9327 ; 1044-7431
    ISSN (online) 1095-9327
    ISSN 1044-7431
    DOI 10.1016/j.mcn.2017.10.004
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  7. Article ; Online: The Ras-like GTPase Rem2 is a potent inhibitor of calcium/calmodulin-dependent kinase II activity.

    Royer, Leandro / Herzog, Josiah J / Kenny, Katelyn / Tzvetkova, Boriana / Cochrane, Jesse C / Marr, Michael T / Paradis, Suzanne

    The Journal of biological chemistry

    2018  Volume 293, Issue 38, Page(s) 14798–14811

    Abstract: ... ...

    Abstract Ca
    MeSH term(s) Animals ; Calcium/metabolism ; Calcium-Calmodulin-Dependent Protein Kinase Type 2/antagonists & inhibitors ; Cells, Cultured ; HEK293 Cells ; Hippocampus/cytology ; Hippocampus/enzymology ; Hippocampus/metabolism ; Homeostasis ; Humans ; Learning ; Long-Term Potentiation ; Memory ; Mice ; Monomeric GTP-Binding Proteins/chemistry ; Monomeric GTP-Binding Proteins/physiology ; Neuronal Plasticity ; Neurons/metabolism ; Phosphorylation ; Substrate Specificity
    Chemical Substances Calcium-Calmodulin-Dependent Protein Kinase Type 2 (EC 2.7.11.17) ; Monomeric GTP-Binding Proteins (EC 3.6.5.2) ; REM2 protein, human (EC 3.6.5.2) ; Rem2 protein, mouse (EC 3.6.5.2) ; Calcium (SY7Q814VUP)
    Language English
    Publishing date 2018-08-02
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 2997-x
    ISSN 1083-351X ; 0021-9258
    ISSN (online) 1083-351X
    ISSN 0021-9258
    DOI 10.1074/jbc.RA118.003560
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  8. Article ; Online: Deconstructing calsequestrin. Complex buffering in the calcium store of skeletal muscle.

    Royer, Leandro / Ríos, Eduardo

    The Journal of physiology

    2009  Volume 587, Issue Pt 13, Page(s) 3101–3111

    Abstract: Since its discovery in 1971, calsequestrin has been recognized as the main Ca(2+) binding protein inside the sarcoplasmic reticulum (SR), the organelle that stores and upon demand mobilizes Ca(2+) for contractile activation of muscle. This article ... ...

    Abstract Since its discovery in 1971, calsequestrin has been recognized as the main Ca(2+) binding protein inside the sarcoplasmic reticulum (SR), the organelle that stores and upon demand mobilizes Ca(2+) for contractile activation of muscle. This article reviews the potential roles of calsequestrin in excitation-contraction coupling of skeletal muscle. It first considers the quantitative demands for a structure that binds Ca(2+) inside the SR in view of the amounts of the ion that must be mobilized to elicit muscle contraction. It briefly discusses existing evidence, largely gathered in cardiac muscle, of two roles for calsequestrin: as Ca(2+) reservoir and as modulator of the activity of Ca(2+) release channels, and then considers the results of an incipient body of work that manipulates the cellular endowment of calsequestrin. The observations include evidence that both the Ca(2+) buffering capacity of calsequestrin in solution and that of the SR in intact cells decay as the free Ca(2+) concentration is lowered. Together with puzzling observations of increase of Ca(2+) inside the SR, in cells or vesicular fractions, upon activation of Ca(2+) release, this is interpreted as evidence that the Ca(2+) buffering in the SR is non-linear, and is optimized for support of Ca(2+) release at the physiological levels of SR Ca(2+) concentration. Such non-linearity of buffering is qualitatively explained by a speculation that puts together ideas first proposed by others. The speculation pictures calsequestrin polymers as 'wires' that both bind Ca(2+) and efficiently deliver it near the release channels. In spite of the kinetic changes, the functional studies reveal that cells devoid of calsequestrin are still capable of releasing large amounts of Ca(2+) into the myoplasm, consistent with the long term viability and apparent good health of mice engineered for calsequestrin ablation. The experiments therefore suggest that other molecules are capable of providing sites for reversible binding of large amounts of Ca(2+) inside the sarcoplasmic reticulum.
    MeSH term(s) Animals ; Binding Sites ; Calcium/metabolism ; Calsequestrin/deficiency ; Calsequestrin/genetics ; Calsequestrin/metabolism ; Mice ; Mice, Knockout ; Models, Biological ; Muscle, Skeletal/metabolism ; Sarcoplasmic Reticulum/metabolism
    Chemical Substances Calsequestrin ; Calcium (SY7Q814VUP)
    Language English
    Publishing date 2009-04-29
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Review
    ZDB-ID 3115-x
    ISSN 1469-7793 ; 0022-3751
    ISSN (online) 1469-7793
    ISSN 0022-3751
    DOI 10.1113/jphysiol.2009.171934
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  9. Article ; Online: Rem2 stabilizes intrinsic excitability and spontaneous firing in visual circuits.

    Moore, Anna R / Richards, Sarah E / Kenny, Katelyn / Royer, Leandro / Chan, Urann / Flavahan, Kelly / Van Hooser, Stephen D / Paradis, Suzanne

    eLife

    2018  Volume 7

    Abstract: Sensory experience plays an important role in shaping neural circuitry by affecting the synaptic connectivity and intrinsic properties of individual neurons. Identifying the molecular players responsible for converting external stimuli into altered ... ...

    Abstract Sensory experience plays an important role in shaping neural circuitry by affecting the synaptic connectivity and intrinsic properties of individual neurons. Identifying the molecular players responsible for converting external stimuli into altered neuronal output remains a crucial step in understanding experience-dependent plasticity and circuit function. Here, we investigate the role of the activity-regulated, non-canonical Ras-like GTPase Rem2 in visual circuit plasticity. We demonstrate that
    MeSH term(s) Action Potentials/physiology ; Animals ; Female ; Gene Expression Regulation ; Male ; Mice ; Mice, Knockout ; Monomeric GTP-Binding Proteins/deficiency ; Monomeric GTP-Binding Proteins/genetics ; Nerve Net/cytology ; Nerve Net/metabolism ; Neuronal Plasticity/genetics ; Primary Cell Culture ; Pyramidal Cells/cytology ; Pyramidal Cells/metabolism ; Rats ; Sensory Receptor Cells/cytology ; Sensory Receptor Cells/metabolism ; Synapses/genetics ; Synapses/metabolism ; Visual Cortex/cytology ; Visual Cortex/metabolism
    Chemical Substances Monomeric GTP-Binding Proteins (EC 3.6.5.2) ; Rem2 protein, mouse (EC 3.6.5.2) ; Rem2 protein, rat (EC 3.6.5.2)
    Language English
    Publishing date 2018-05-29
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2687154-3
    ISSN 2050-084X ; 2050-084X
    ISSN (online) 2050-084X
    ISSN 2050-084X
    DOI 10.7554/eLife.33092
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  10. Article ; Online: Rem2 stabilizes intrinsic excitability and spontaneous firing in visual circuits

    Anna R Moore / Sarah E Richards / Katelyn Kenny / Leandro Royer / Urann Chan / Kelly Flavahan / Stephen D Van Hooser / Suzanne Paradis

    eLife, Vol

    2018  Volume 7

    Abstract: Sensory experience plays an important role in shaping neural circuitry by affecting the synaptic connectivity and intrinsic properties of individual neurons. Identifying the molecular players responsible for converting external stimuli into altered ... ...

    Abstract Sensory experience plays an important role in shaping neural circuitry by affecting the synaptic connectivity and intrinsic properties of individual neurons. Identifying the molecular players responsible for converting external stimuli into altered neuronal output remains a crucial step in understanding experience-dependent plasticity and circuit function. Here, we investigate the role of the activity-regulated, non-canonical Ras-like GTPase Rem2 in visual circuit plasticity. We demonstrate that Rem2-/- mice fail to exhibit normal ocular dominance plasticity during the critical period. At the cellular level, our data establish a cell-autonomous role for Rem2 in regulating intrinsic excitability of layer 2/3 pyramidal neurons, prior to changes in synaptic function. Consistent with these findings, both in vitro and in vivo recordings reveal increased spontaneous firing rates in the absence of Rem2. Taken together, our data demonstrate that Rem2 is a key molecule that regulates neuronal excitability and circuit function in the context of changing sensory experience.
    Keywords intrinsic excitability ; Rem2 ; plasticity ; activity-dependent ; homeostasis ; Medicine ; R ; Science ; Q ; Biology (General) ; QH301-705.5
    Subject code 612
    Language English
    Publishing date 2018-05-01T00:00:00Z
    Publisher eLife Sciences Publications Ltd
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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