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1.
Front Neuroanat ; 17: 1302373, 2023.
Article in English | MEDLINE | ID: mdl-38164516

ABSTRACT

Introduction: Satellite glial cells (SGCs) that envelop the cell bodies of neurons in sensory ganglia have been shown to both release glutamate, and be activated by glutamate in the context of nociceptive signaling. However, little is known about the subpopulations of SGCs that are activated following nerve injury and whether glutamate mechanisms in the SGCs are involved in the pathologic pain. Methods: To address this issue, we used light and electron microscopic immunohistochemistry to examine the change in the glutamate levels in the SGCs and the structural relationship between neighboring neurons in the trigeminal ganglion (TG) in a rat model of craniofacial neuropathic pain, CCI-ION. Results: Administration of ionomycin, ATP and Bz-ATP induced an increase of extracellular glutamate concentration in cultured trigeminal SGCs, indicating a release of glutamate from SGCs. The level of glutamate immunostaining in the SGCs that envelop neurons of all sizes in the TG was significantly higher in rats with CCI-ION than in control rats, suggesting that SGCs enveloping nociceptive as well as non-nociceptive mechanosensitive neurons are activated following nerve injury, and that the glutamate release from SGCs increases in pathologic pain state. Close appositions between substance-P (SP)-immunopositive (+) or calcitonin gene-related peptide (CGRP)+, likely nociceptive neurons, between Piezo1+, likely non-nociceptive, mechanosensitive neurons and SP+ or CGRP+ neurons, and between SGCs of neighboring neurons were frequently observed. Discussion: These findings suggest that glutamate in the trigeminal SGCs that envelop all types of neurons may play a role in the mechanisms of neuropathic pain, possibly via paracrine signaling.

2.
Nat Commun ; 12(1): 3968, 2021 06 25.
Article in English | MEDLINE | ID: mdl-34172755

ABSTRACT

Cellular heterogeneity in the human brain obscures the identification of robust cellular regulatory networks, which is necessary to understand the function of non-coding elements and the impact of non-coding genetic variation. Here we integrate genome-wide chromosome conformation data from purified neurons and glia with transcriptomic and enhancer profiles, to characterize the gene regulatory landscape of two major cell classes in the human brain. We then leverage cell-type-specific regulatory landscapes to gain insight into the cellular etiology of several brain disorders. We find that Alzheimer's disease (AD)-associated epigenetic dysregulation is linked to neurons and oligodendrocytes, whereas genetic risk factors for AD highlighted microglia, suggesting that different cell types may contribute to disease risk, via different mechanisms. Moreover, integration of glutamatergic and GABAergic regulatory maps with genetic risk factors for schizophrenia (SCZ) and bipolar disorder (BD) identifies shared (parvalbumin-expressing interneurons) and distinct cellular etiologies (upper layer neurons for BD, and deeper layer projection neurons for SCZ). Collectively, these findings shed new light on cell-type-specific gene regulatory networks in brain disorders.


Subject(s)
Alzheimer Disease/genetics , Bipolar Disorder/genetics , Chromatin/ultrastructure , Schizophrenia/genetics , Acetylation , Alzheimer Disease/pathology , Bipolar Disorder/pathology , Chromatin/chemistry , Chromatin/genetics , Chromatin/metabolism , Chromatin Immunoprecipitation Sequencing , Enhancer Elements, Genetic , Epigenesis, Genetic , GABAergic Neurons/metabolism , Gene Expression Regulation , Genome-Wide Association Study , Histones/metabolism , Humans , Lysine/metabolism , Neuroglia/pathology , Neuroglia/ultrastructure , Neurons/pathology , Neurons/ultrastructure , Promoter Regions, Genetic , Schizophrenia/pathology
3.
Nat Neurosci ; 23(4): 583-593, 2020 04.
Article in English | MEDLINE | ID: mdl-32152537

ABSTRACT

Most risk variants for brain disorders identified by genome-wide association studies reside in the noncoding genome, which makes deciphering biological mechanisms difficult. A commonly used tool, multimarker analysis of genomic annotation (MAGMA), addresses this issue by aggregating single nucleotide polymorphism associations to nearest genes. Here we developed a platform, Hi-C-coupled MAGMA (H-MAGMA), that advances MAGMA by incorporating chromatin interaction profiles from human brain tissue across two developmental epochs and two brain cell types. By analyzing gene regulatory relationships in the disease-relevant tissue, H-MAGMA identified neurobiologically relevant target genes. We applied H-MAGMA to five psychiatric disorders and four neurodegenerative disorders to interrogate biological pathways, developmental windows and cell types implicated for each disorder. Psychiatric-disorder risk genes tended to be expressed during mid-gestation and in excitatory neurons, whereas neurodegenerative-disorder risk genes showed increasing expression over time and more diverse cell-type specificities. H-MAGMA adds to existing analytic frameworks to help identify the neurobiological principles of brain disorders.


Subject(s)
Brain Diseases/genetics , Brain/metabolism , Chromatin/metabolism , Genetic Predisposition to Disease , Polymorphism, Single Nucleotide , Brain Diseases/metabolism , Genomics , Humans , Risk Factors
4.
Schizophr Res ; 217: 17-25, 2020 03.
Article in English | MEDLINE | ID: mdl-30894290

ABSTRACT

Recent advances in our understanding of the genetic architecture of schizophrenia have shed light on the schizophrenia etiology. While common variation is one of the major genetic contributors, the majority of common variation reside in non-coding genome, posing a significant challenge in understanding the functional impact of this class of genetic variation. Functional genomic datasets that range from expression quantitative trait loci (eQTL) to chromatin interactions are critical to identify the potential target genes and functional consequences of non-coding variation. In this review, we discuss how three-dimensional chromatin landscape, identified by a technique called Hi-C, has facilitated the identification of potential target genes impacting schizophrenia risk. We outline key steps for Hi-C driven gene mapping, and compare Hi-C defined schizophrenia risk genes defined across developmental epochs and cell types, which offer rich insights into the temporal window and cellular etiology of schizophrenia. In contrast with a neurodevelopmental hypothesis in schizophrenia, Hi-C defined schizophrenia risk genes are postnatally enriched, suggesting that postnatal development is also important for schizophrenia pathogenesis. Moreover, Hi-C defined schizophrenia risk genes are highly expressed in excitatory neurons, highlighting excitatory neurons as a central cell type for schizophrenia. Further characterization of Hi-C defined schizophrenia risk genes demonstrated enrichment for genes that harbor loss-of-function variation in neurodevelopmental disorders, suggesting a shared genetic etiology between schizophrenia and neurodevelopmental disorders. Collectively, moving the search space from risk variants to the target genes lays a foundation to understand the neurobiological basis of schizophrenia.


Subject(s)
Schizophrenia , Brain , Chromatin , Genome , Genome-Wide Association Study , Humans , Polymorphism, Single Nucleotide , Schizophrenia/genetics
5.
Biol Psychiatry ; 85(7): 534-543, 2019 04 01.
Article in English | MEDLINE | ID: mdl-30466882

ABSTRACT

BACKGROUND: Autism spectrum disorder involves neurodevelopmental dysregulations that lead to visible symptoms at early stages of life. Many autism spectrum disorder-related mechanisms suggested by animal studies are supported by demonstrated improvement in autistic-like phenotypes in adult animals following experimental reversal of dysregulated mechanisms. However, whether such mechanisms also act at earlier stages to cause autistic-like phenotypes is unclear. METHODS: We used Shank2-/- mice carrying a mutation identified in human autism spectrum disorder (exons 6 and 7 deletion) and combined electrophysiological and behavioral analyses to see whether early pathophysiology at pup stages is different from late pathophysiology at juvenile and adult stages and whether correcting early pathophysiology can normalize late pathophysiology and abnormal behaviors in juvenile and adult mice. RESULTS: Early correction of a dysregulated mechanism in young mice prevents manifestation of autistic-like social behaviors in adult mice. Shank2-/- mice, known to display N-methyl-D-aspartate receptor (NMDAR) hypofunction and autistic-like behaviors at postweaning stages after postnatal day 21 (P21), show the opposite synaptic phenotype-NMDAR hyperfunction-at an earlier preweaning stage (∼P14). Moreover, this NMDAR hyperfunction at P14 rapidly shifts to NMDAR hypofunction after weaning (∼P24). Chronic suppression of the early NMDAR hyperfunction by the NMDAR antagonist memantine (P7-P21) prevents NMDAR hypofunction and autistic-like social behaviors from manifesting at later stages (∼P28 and P56). CONCLUSIONS: Early NMDAR hyperfunction leads to late NMDAR hypofunction and autistic-like social behaviors in Shank2-/- mice, and early correction of NMDAR dysfunction has the long-lasting effect of preventing autistic-like social behaviors from developing at later stages.


Subject(s)
Autism Spectrum Disorder/drug therapy , Autism Spectrum Disorder/physiopathology , Behavior, Animal/drug effects , Excitatory Amino Acid Antagonists/pharmacology , Memantine/pharmacology , Receptors, N-Methyl-D-Aspartate/drug effects , Social Behavior , Age Factors , Animals , Behavior, Animal/physiology , Disease Models, Animal , Mice , Mice, Inbred C57BL , Mice, Knockout , Nerve Tissue Proteins , Receptors, N-Methyl-D-Aspartate/antagonists & inhibitors , Receptors, N-Methyl-D-Aspartate/physiology
6.
Nat Neurosci ; 21(9): 1218-1228, 2018 09.
Article in English | MEDLINE | ID: mdl-30104731

ABSTRACT

Autism spectrum disorders (ASDs) are four times more common in males than in females, but the underlying mechanisms are poorly understood. We characterized sexually dimorphic changes in mice carrying a heterozygous mutation in Chd8 (Chd8+/N2373K) that was first identified in human CHD8 (Asn2373LysfsX2), a strong ASD-risk gene that encodes a chromatin remodeler. Notably, although male mutant mice displayed a range of abnormal behaviors during pup, juvenile, and adult stages, including enhanced mother-seeking ultrasonic vocalization, enhanced attachment to reunited mothers, and isolation-induced self-grooming, their female counterparts do not. This behavioral divergence was associated with sexually dimorphic changes in neuronal activity, synaptic transmission, and transcriptomic profiles. Specifically, female mice displayed suppressed baseline neuronal excitation, enhanced inhibitory synaptic transmission and neuronal firing, and increased expression of genes associated with extracellular vesicles and the extracellular matrix. Our results suggest that a human CHD8 mutation leads to sexually dimorphic changes ranging from transcription to behavior in mice.


Subject(s)
Behavior, Animal/physiology , DNA-Binding Proteins/biosynthesis , Gene Expression/physiology , Neurons/physiology , Sex Characteristics , Animals , Anxiety, Separation/genetics , Anxiety, Separation/psychology , DNA-Binding Proteins/genetics , Extracellular Matrix/metabolism , Extracellular Matrix/physiology , Female , Hippocampus/physiology , Male , Mice , Mice, Inbred C57BL , Object Attachment , Signal Transduction/physiology , Social Behavior , Synaptic Transmission/genetics , Synaptic Transmission/physiology , Transcriptome , Vocalization, Animal
7.
Sci Rep ; 7(1): 13627, 2017 10 19.
Article in English | MEDLINE | ID: mdl-29051582

ABSTRACT

The purinergic receptor P2X3, expressed in the central terminals of primary nociceptive neurons in the brainstem, plays an important role in pathological pain. However, little is known about expression of P2X3 in the brainstem astrocytes and its involvement in craniofacial pathologic pain. To address this issue, we investigated the expression of P2X3 in astrocytes in the trigeminal caudal nucleus (Vc) in a rat model of craniofacial neuropathic pain, chronic constriction injury of infraorbital nerve (CCI-ION). We found that 1) P2X3-immunoreactivity is observed in the brainstem astrocytes, preferentially in their fine processes, 2) the number of P2X3-positive fine astrocytic processes and the density of P2X3 in these processes were increased significantly in CCI-ION rats, compared to control rats, and 3) administration of MPEP, a specific mGluR5 antagonist, alleviated the mechanical allodynia and abolished the increase in density of P2X3 in fine astrocytic processes caused by CCI-ION. These findings reveal preferential expression of P2X3 in the fine astrocytic processes in the brainstem, propose a novel role of P2X3 in the fine astrocytic process in the mechanism of craniofacial neuropathic pain, and suggest that the expression of astrocytic P2X3 may be regulated by astrocytic mGluR5.


Subject(s)
Facial Pain/pathology , Receptors, Purinergic P2X3/metabolism , Animals , Astrocytes/cytology , Astrocytes/metabolism , Brain Stem/metabolism , Disease Models, Animal , Facial Pain/complications , Facial Pain/metabolism , Gene Expression Regulation/drug effects , Glial Fibrillary Acidic Protein/metabolism , Hyperalgesia/etiology , Male , Microscopy, Electron , Pyridines/pharmacology , Rats , Rats, Sprague-Dawley , Receptors, Purinergic P2X3/genetics
8.
Nat Commun ; 7: 12328, 2016 08 02.
Article in English | MEDLINE | ID: mdl-27480238

ABSTRACT

Synaptic adhesion molecules regulate various aspects of synapse development, function and plasticity. These functions mainly involve trans-synaptic interactions and positive regulations, whereas cis-interactions and negative regulation are less understood. Here we report that SALM4, a member of the SALM/Lrfn family of synaptic adhesion molecules, suppresses excitatory synapse development through cis inhibition of SALM3, another SALM family protein with synaptogenic activity. Salm4-mutant (Salm4(-/-)) mice show increased excitatory synapse numbers in the hippocampus. SALM4 cis-interacts with SALM3, inhibits trans-synaptic SALM3 interaction with presynaptic LAR family receptor tyrosine phosphatases and suppresses SALM3-dependent presynaptic differentiation. Importantly, deletion of Salm3 in Salm4(-/-) mice (Salm3(-/-); Salm4(-/-)) normalizes the increased excitatory synapse number. These results suggest that SALM4 negatively regulates excitatory synapses via cis inhibition of the trans-synaptic SALM3-LAR adhesion.


Subject(s)
Cell Adhesion Molecules, Neuronal/metabolism , Cell Differentiation/physiology , Neural Cell Adhesion Molecules/metabolism , Presynaptic Terminals/physiology , Pyramidal Cells/physiology , Receptor-Like Protein Tyrosine Phosphatases, Class 2/metabolism , Animals , CA1 Region, Hippocampal/cytology , CA1 Region, Hippocampal/physiology , Cell Adhesion/physiology , Cell Adhesion Molecules, Neuronal/genetics , Excitatory Postsynaptic Potentials/physiology , Female , Male , Membrane Glycoproteins , Mice , Mice, Inbred C57BL , Mice, Knockout , Models, Animal , Nerve Tissue Proteins , Neural Cell Adhesion Molecules/genetics , Synaptic Transmission/physiology
9.
Sci Rep ; 6: 26676, 2016 05 26.
Article in English | MEDLINE | ID: mdl-27225731

ABSTRACT

Synaptogenic adhesion molecules play critical roles in synapse formation. SALM5/Lrfn5, a SALM/Lrfn family adhesion molecule implicated in autism spectrum disorders (ASDs) and schizophrenia, induces presynaptic differentiation in contacting axons, but its presynaptic ligand remains unknown. We found that SALM5 interacts with the Ig domains of LAR family receptor protein tyrosine phosphatases (LAR-RPTPs; LAR, PTPδ, and PTPσ). These interactions are strongly inhibited by the splice insert B in the Ig domain region of LAR-RPTPs, and mediate SALM5-dependent presynaptic differentiation in contacting axons. In addition, SALM5 regulates AMPA receptor-mediated synaptic transmission through mechanisms involving the interaction of postsynaptic SALM5 with presynaptic LAR-RPTPs. These results suggest that postsynaptic SALM5 promotes synapse development by trans-synaptically interacting with presynaptic LAR-RPTPs and is important for the regulation of excitatory synaptic strength.


Subject(s)
Alternative Splicing/physiology , Axons/metabolism , Cell Adhesion Molecules, Neuronal/metabolism , Receptor-Like Protein Tyrosine Phosphatases, Class 2/metabolism , Synapses/metabolism , Synaptic Transmission/physiology , Animals , Cell Adhesion Molecules, Neuronal/genetics , Mice , Receptor-Like Protein Tyrosine Phosphatases, Class 2/genetics , Synapses/genetics
10.
Brain Struct Funct ; 221(9): 4601-4613, 2016 12.
Article in English | MEDLINE | ID: mdl-26832918

ABSTRACT

Increasing evidence shows that the homomeric glycine receptor is expressed in axon terminals and is involved in the presynaptic modulation of transmitter release. However, little is known about the expression of the glycine receptor, implicated in the presynaptic modulation of sensory transmission in the primary somatosensory neurons and their central boutons. To address this, we investigated the expression of glycine receptor subunit alpha 3 (GlyRα3) in the neurons in the trigeminal ganglion and axon terminals in the 1st relay nucleus of the brainstem by light- and electron-microscopic immunohistochemistry. Trigeminal primary sensory neurons were GlyRα3-immunopositive/gephyrin-immunonegative (indicating homomeric GlyR), whereas GlyRα3/gephyrin immunoreactivity (indicating heteromeric GlyR) was observed in dendrites. GlyRα3 immunoreactivity was also found in the central boutons of primary afferents but far from the presynaptic site and in dendrites at subsynaptic sites. Boutons expressing GlyRα3 contained small round vesicles, formed asymmetric synapses with dendrites and were immunoreactive for glutamate. These findings suggest that trigeminal primary afferent boutons receive presynaptic modulation via homomeric, extrasynaptic GlyRα3, and that different subtypes of GlyR may be involved in pre- and postsynaptic inhibition.


Subject(s)
Brain Stem/ultrastructure , Presynaptic Terminals/metabolism , Presynaptic Terminals/ultrastructure , Receptors, Glycine/metabolism , Trigeminal Ganglion/metabolism , Trigeminal Ganglion/ultrastructure , Animals , Brain Stem/metabolism , Carrier Proteins/metabolism , Male , Membrane Proteins/metabolism , Rats , Rats, Sprague-Dawley
11.
Nat Neurosci ; 19(1): 84-93, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26595655

ABSTRACT

Synaptic adhesion molecules regulate synapse development and plasticity through mechanisms that include trans-synaptic adhesion and recruitment of diverse synaptic proteins. We found that the immunoglobulin superfamily member 11 (IgSF11), a homophilic adhesion molecule that preferentially expressed in the brain, is a dual-binding partner of the postsynaptic scaffolding protein PSD-95 and AMPA glutamate receptors (AMPARs). IgSF11 required PSD-95 binding for its excitatory synaptic localization. In addition, IgSF11 stabilized synaptic AMPARs, as determined by IgSF11 knockdown-induced suppression of AMPAR-mediated synaptic transmission and increased surface mobility of AMPARs, measured by high-throughput, single-molecule tracking. IgSF11 deletion in mice led to the suppression of AMPAR-mediated synaptic transmission in the dentate gyrus and long-term potentiation in the CA1 region of the hippocampus. IgSF11 did not regulate the functional characteristics of AMPARs, including desensitization, deactivation or recovery. These results suggest that IgSF11 regulates excitatory synaptic transmission and plasticity through its tripartite interactions with PSD-95 and AMPARs.


Subject(s)
Cell Adhesion Molecules, Neuronal/physiology , Cell Adhesion Molecules/physiology , Gene Expression Regulation/physiology , Hippocampus/metabolism , Immunoglobulins/physiology , Intracellular Signaling Peptides and Proteins/metabolism , Membrane Proteins/metabolism , Neuronal Plasticity/physiology , Neurons/metabolism , Receptors, AMPA/metabolism , Synaptic Transmission/physiology , Animals , Cell Adhesion Molecules/metabolism , Cells, Cultured , Disks Large Homolog 4 Protein , Gene Knockdown Techniques , Guinea Pigs , Humans , Immunoglobulins/metabolism , Mice , Patch-Clamp Techniques , Rabbits , Rats , Rats, Sprague-Dawley
12.
Cell Rep ; 12(10): 1618-30, 2015 Sep 08.
Article in English | MEDLINE | ID: mdl-26321637

ABSTRACT

Synaptic adhesion molecules regulate diverse aspects of synapse development and plasticity. SALM3 is a PSD-95-interacting synaptic adhesion molecule known to induce presynaptic differentiation in contacting axons, but little is known about its presynaptic receptors and in vivo functions. Here, we identify an interaction between SALM3 and LAR family receptor protein tyrosine phosphatases (LAR-RPTPs) that requires the mini-exon B splice insert in LAR-RPTPs. In addition, SALM3-dependent presynaptic differentiation requires all three types of LAR-RPTPs. SALM3 mutant (Salm3(-/-)) mice display markedly reduced excitatory synapse number but normal synaptic plasticity in the hippocampal CA1 region. Salm3(-/-) mice exhibit hypoactivity in both novel and familiar environments but perform normally in learning and memory tests administered. These results suggest that SALM3 regulates excitatory synapse development and locomotion behavior.


Subject(s)
Neural Cell Adhesion Molecules/physiology , Receptor-Like Protein Tyrosine Phosphatases, Class 2/metabolism , Synapses/physiology , Alternative Splicing , Animals , Cell Differentiation , Excitatory Postsynaptic Potentials , Exons , Hippocampus/cytology , Hippocampus/metabolism , Learning , Locomotion , Membrane Glycoproteins , Mice, Knockout , Nerve Tissue Proteins , Neuronal Plasticity , Protein Isoforms/physiology , Psychomotor Performance , RNA Splice Sites , Synaptic Transmission
13.
Exp Neurobiol ; 24(2): 126-32, 2015 Jun.
Article in English | MEDLINE | ID: mdl-26113791

ABSTRACT

Cross-talk between the thalamus and cortex has been implicated in attention but its pathogenic role in attention-deficit/hyperactivity disorder (ADHD) remains unknown. Here, I demonstrate that Git1 (-/-) mice, previously proposed as an animal model for ADHD, show abnormal theta oscillation in the thalamus. Multi-electrode recordings revealed that Git1 (-/-) mice have hyper-synchrony of neural activities between the thalamus and cortex. The abnormal thalamic oscillation and thalamocortical synchrony in Git1 (-/-) mice were markedly reduced by amphetamine. In addition, ethosuximide ameliorates abnormal thalamic oscillation and ADHD-like hyperactivity shown in Git1 (-/-) mice. My study suggests critical roles of GIT1 and thalamocortical neural circuitry in ADHD.

14.
Mol Cells ; 38(6): 540-7, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25997734

ABSTRACT

Attention deficit/hyperactivity disorder (ADHD) is one of the most common neurodevelopmental disorders, affecting approximately 5% of children. However, the neural mechanisms underlying its development and treatment are yet to be elucidated. In this study, we report that an ADHD mouse model, which harbors a deletion in the Git1 locus, exhibits severe astrocytosis in the globus pallidus (GP) and thalamic reticular nucleus (TRN), which send modulatory GABAergic inputs to the thalamus. A moderate level of astrocytosis was displayed in other regions of the basal ganglia pathway, including the ventrobasal thalamus and cortex, but not in other brain regions, such as the caudate putamen, basolateral amygdala, and hippocampal CA1. This basal ganglia circuit-selective astrocytosis was detected in both in adult (2-3 months old) and juvenile (4 weeks old) Git1(-/-) mice, suggesting a developmental origin. Astrocytes play an active role in the developing synaptic circuit; therefore, we performed an immunohistochemical analysis of synaptic markers. We detected increased and decreased levels of GABA and parvalbumin (PV), respectively, in the GP. This suggests that astrocytosis may alter synaptic transmission in the basal ganglia. Intriguingly, increased GABA expression colocalized with the astrocyte marker, GFAP, indicative of an astrocytic origin. Collectively, these results suggest that defects in basal ganglia circuitry, leading to impaired inhibitory modulation of the thalamus, are neural correlates for the ADHD-associated behavioral manifestations in Git1(-/-) mice.


Subject(s)
Attention Deficit Disorder with Hyperactivity/pathology , Basal Ganglia/pathology , Cell Cycle Proteins/genetics , GTPase-Activating Proteins/genetics , Gliosis/pathology , Animals , Attention Deficit Disorder with Hyperactivity/genetics , Cell Cycle Proteins/metabolism , GTPase-Activating Proteins/metabolism , Gliosis/genetics , Mice , Mice, Transgenic , Synaptic Transmission
15.
Exp Neurobiol ; 24(1): 8-16, 2015 Mar.
Article in English | MEDLINE | ID: mdl-25792865

ABSTRACT

GIT1, a multifunctional signaling adaptor protein, is implicated in the development of dendritic spines and neuronal synapses. GIT1 forms a signaling complex with PIX, RAC, and PAK proteins that is known to play important roles in brain development. Here we found that Git1-knockout (Git1(-/-) ) mice show a microcephaly-like small brain phenotype, which appears to be caused by reduced neuronal size rather than number. Git1(-/-) mice also show decreased dendritic spine number without morphological alterations in the hippocampus. Behaviorally, Git1(-/-) mice show impaired motor coordination and learning and memory. In addition, adult dGit Drosophila mutants show decreased brain size and abnormal morphology of the mushroom body. These results suggest that GIT1 is important for brain development in both rodents and flies.

16.
J Comp Neurol ; 523(1): 126-38, 2015 Jan 01.
Article in English | MEDLINE | ID: mdl-25185935

ABSTRACT

Substance P (SP), calcitonin gene-related peptide (CGRP), and isolectin B4 (IB4) are widely used as markers for peripheral neurons with unmyelinated fibers, whereas neurofilament 200 (NF200), and Peripherin are used as markers for neurons with myelinated fibers, and with unmyelinated or small-caliber fibers, respectively. To study the selectivity of these markers for specific neuronal types, we analyzed their expression in neurons in the rat trigeminal ganglion by light- and electron-microscopic immunocytochemistry. Most SP-immunopositive (+), CGRP+, and IB4+ fibers were unmyelinated, but a small fraction (∼5%) were small myelinated fibers (<20 µm(2) in cross-sectional area, equivalent to <5 µm in diameter, Aδ fiber). Similarly, whereas the majority of NF200+ fibers were myelinated, a large fraction (23.9%) were unmyelinated, and whereas the majority of Peripherin+ fibers were unmyelinated and small myelinated, a significant fraction (15.5%) were large myelinated (>20 µm(2) in cross-sectional area, equivalent to >5 µm in diameter, Aß fiber). Our findings confirm that SP, CGRP, and IB4 can be used as reliable markers for neurons with unmyelinated fibers, and question the suitability of NF200 as a marker for neurons with myelinated fibers, and of Peripherin as a marker for neurons with unmyelinated, or fine-caliber fibers.


Subject(s)
Neurons, Afferent/metabolism , Trigeminal Ganglion/metabolism , Animals , Calcitonin Gene-Related Peptide/metabolism , Cell Size , Immunohistochemistry , Lectins/metabolism , Male , Microscopy, Electron , Nerve Fibers, Myelinated/metabolism , Neurofilament Proteins/metabolism , Neurons/cytology , Neurons/metabolism , Neurons, Afferent/cytology , Peptide Fragments/metabolism , Peripherins/metabolism , Rats, Sprague-Dawley , Substance P/metabolism , Trigeminal Ganglion/cytology
17.
Front Mol Neurosci ; 6: 19, 2013.
Article in English | MEDLINE | ID: mdl-23935565

ABSTRACT

Autism spectrum disorder (ASD) is a group of developmental disabilities characterized by impairments in social interaction and communication and restricted and repetitive interests/behaviors. Advances in human genomics have identified a large number of genetic variations associated with ASD. These associations are being rapidly verified by a growing number of studies using a variety of approaches, including mouse genetics. These studies have also identified key mechanisms underlying the pathogenesis of ASD, many of which involve synaptic dysfunctions, and have investigated novel, mechanism-based therapeutic strategies. This review will try to integrate these three key aspects of ASD research: human genetics, animal models, and potential treatments. Continued efforts in this direction should ultimately reveal core mechanisms that account for a larger fraction of ASD cases and identify neural mechanisms associated with specific ASD symptoms, providing important clues to efficient ASD treatment.

18.
Nature ; 486(7402): 261-5, 2012 Jun 13.
Article in English | MEDLINE | ID: mdl-22699620

ABSTRACT

Autism spectrum disorder (ASD) is a group of conditions characterized by impaired social interaction and communication, and restricted and repetitive behaviours. ASD is a highly heritable disorder involving various genetic determinants. Shank2 (also known as ProSAP1) is a multi-domain scaffolding protein and signalling adaptor enriched at excitatory neuronal synapses, and mutations in the human SHANK2 gene have recently been associated with ASD and intellectual disability. Although ASD-associated genes are being increasingly identified and studied using various approaches, including mouse genetics, further efforts are required to delineate important causal mechanisms with the potential for therapeutic application. Here we show that Shank2-mutant (Shank2(-/-)) mice carrying a mutation identical to the ASD-associated microdeletion in the human SHANK2 gene exhibit ASD-like behaviours including reduced social interaction, reduced social communication by ultrasonic vocalizations, and repetitive jumping. These mice show a marked decrease in NMDA (N-methyl-D-aspartate) glutamate receptor (NMDAR) function. Direct stimulation of NMDARs with D-cycloserine, a partial agonist of NMDARs, normalizes NMDAR function and improves social interaction in Shank2(-/-) mice. Furthermore, treatment of Shank2(-/-) mice with a positive allosteric modulator of metabotropic glutamate receptor 5 (mGluR5), which enhances NMDAR function via mGluR5 activation, also normalizes NMDAR function and markedly enhances social interaction. These results suggest that reduced NMDAR function may contribute to the development of ASD-like phenotypes in Shank2(-/-) mice, and mGluR modulation of NMDARs offers a potential strategy to treat ASD.


Subject(s)
Adaptor Proteins, Signal Transducing/genetics , Autistic Disorder , Behavior, Animal/drug effects , Benzamides/pharmacology , Cycloserine/pharmacology , Nerve Tissue Proteins/genetics , Pyrazoles/pharmacology , Receptors, N-Methyl-D-Aspartate/agonists , Receptors, N-Methyl-D-Aspartate/metabolism , Animals , Antimetabolites/pharmacology , Autistic Disorder/genetics , Autistic Disorder/metabolism , Behavior, Animal/physiology , Disease Models, Animal , Female , Male , Mice , Mice, Inbred C57BL
19.
Semin Cell Dev Biol ; 22(5): 492-8, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21736948

ABSTRACT

Synaptic adhesion molecules play important roles in various stages of neuronal development, including neurite outgrowth and synapse formation. The SALM (synaptic adhesion-like molecule) family of adhesion molecules, also known as Lrfn, belongs to the superfamily of leucine-rich repeat (LRR)-containing adhesion molecules. Proteins of the SALM family, which includes five known members (SALMs 1-5), have been implicated in the regulation of neurite outgrowth and branching, and synapse formation and maturation. Despite sharing a similar domain structure, individual SALM family proteins appear to have distinct functions. SALMs 1-3 contain a C-terminal PDZ-binding motif, which interacts with PSD-95, an abundant postsynaptic scaffolding protein, whereas SALM4 and SALM5 lack PDZ binding. SALM1 directly interacts with NMDA receptors but not with AMPA receptors, whereas SALM2 associates with both NMDA and AMPA receptors. SALMs 1-3 form homo- and heteromeric complexes with each other in a cis manner, whereas SALM4 and SALM5 do not, but instead participate in homophilic, trans-cellular adhesion. SALM3 and SALM5, but not other SALMs, possess synaptogenic activity, inducing presynaptic differentiation in contacting axons. All SALMs promote neurite outgrowth, while SALM4 uniquely increases the number of primary processes extending from the cell body. In addition to these functional diversities, the fifth member of the SALM family, SALM5/Lrfn5, has recently been implicated in severe progressive autism and familial schizophrenia, pointing to the clinical importance of SALMs.


Subject(s)
Cell Adhesion Molecules, Neuronal/chemistry , Cell Adhesion Molecules, Neuronal/metabolism , Membrane Glycoproteins/metabolism , Nerve Tissue Proteins/metabolism , Proteins/metabolism , Synapses/metabolism , Amino Acid Sequence , Autistic Disorder/genetics , Carrier Proteins/chemistry , Carrier Proteins/metabolism , Disks Large Homolog 4 Protein , Humans , Intracellular Signaling Peptides and Proteins/chemistry , Intracellular Signaling Peptides and Proteins/metabolism , Leucine-Rich Repeat Proteins , Membrane Glycoproteins/chemistry , Membrane Proteins/chemistry , Membrane Proteins/metabolism , Molecular Sequence Data , Nerve Tissue Proteins/chemistry , Proteins/chemistry , Receptors, AMPA/chemistry , Receptors, AMPA/metabolism , Receptors, N-Methyl-D-Aspartate/chemistry , Receptors, N-Methyl-D-Aspartate/metabolism , Schizophrenia/genetics
20.
Nat Med ; 17(5): 566-72, 2011 May.
Article in English | MEDLINE | ID: mdl-21499268

ABSTRACT

Attention deficit hyperactivity disorder (ADHD) is a psychiatric disorder that affects ~5% of school-aged children; however, the mechanisms underlying ADHD remain largely unclear. Here we report a previously unidentified association between G protein-coupled receptor kinase-interacting protein-1 (GIT1) and ADHD in humans. An intronic single-nucleotide polymorphism in GIT1, the minor allele of which causes reduced GIT1 expression, shows a strong association with ADHD susceptibility in humans. Git1-deficient mice show ADHD-like phenotypes, with traits including hyperactivity, enhanced electroencephalogram theta rhythms and impaired learning and memory. Hyperactivity in Git1(-/-) mice is reversed by amphetamine and methylphenidate, psychostimulants commonly used to treat ADHD. In addition, amphetamine normalizes enhanced theta rhythms and impaired memory. GIT1 deficiency in mice leads to decreases in ras-related C3 botulinum toxin substrate-1 (RAC1) signaling and inhibitory presynaptic input; furthermore, it shifts the neuronal excitation-inhibition balance in postsynaptic neurons toward excitation. Our study identifies a previously unknown involvement of GIT1 in human ADHD and shows that GIT1 deficiency in mice causes psychostimulant-responsive ADHD-like phenotypes.


Subject(s)
Adaptor Proteins, Signal Transducing/genetics , Attention Deficit Disorder with Hyperactivity/genetics , Cell Cycle Proteins/genetics , GTPase-Activating Proteins/deficiency , GTPase-Activating Proteins/genetics , Adaptor Proteins, Signal Transducing/physiology , Amphetamine/pharmacology , Animals , Attention Deficit Disorder with Hyperactivity/drug therapy , Attention Deficit Disorder with Hyperactivity/physiopathology , Attention Deficit Disorder with Hyperactivity/psychology , Brain/physiopathology , Cell Cycle Proteins/physiology , Central Nervous System Stimulants/pharmacology , Child , Disease Models, Animal , Electroencephalography , Female , Genetic Predisposition to Disease , Humans , Male , Memory Disorders/drug therapy , Memory Disorders/genetics , Memory Disorders/psychology , Methylphenidate/pharmacology , Mice , Mice, Knockout , Motor Activity/drug effects , Motor Activity/genetics , Motor Activity/physiology , Neuropeptides/metabolism , Phenotype , Polymorphism, Single Nucleotide , Signal Transduction , Synaptic Transmission , rac GTP-Binding Proteins/metabolism , rac1 GTP-Binding Protein
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