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Chaterjee, I.

Publications and source records attributed to Chaterjee, I..

3 recordsLinked to original sources

CTCF regulates anxiety and depression like behavior and maintenance of neuronal identity in the adult mouse brain

CCCTC-binding factor (CTCF) is a chromatin binding factor that binds to DNA sequence specific sites and, together with cohesin complex, establishes chromatin loops and regulates gene expression. CTCF was previously implicated as a major contributor in neural development. Genetic aberrations in CTCF are associated with intellectual disability, aggression, attention deficit, and autistic behavior. Previous mice-model studies have identified a necessary role for CTCF during development of CaMKIIa expressing excitatory neurons in the ability of learning and memory. However, it is not clear if CTCF is only necessary for development in the brain, or also in maintenance of neuronal functions and behavior in the adulthood. In the current study, adulthood-specific knockout of CTCF in excitatory neurons induced an elevation in anxiety and depression related behavior and a decrease in seeking social novelty. Depression and apathy-like behavior was reversed by treatment with serotonin specific reuptake inhibitor sertraline. Golgi staining analysis reveals major regression of dendritic complexity in the hippocampus and prefrontal cortex. In parallel, there is increased DNA compaction and decreased global H3K9 acetylation. Single nuclei RNA sequencing confirms a retreat in neuronal subtype identity in excitatory neurons after knockout. Gene ontology analysis display upregulation of genes that related regulation of cell population, neuronal development and neuronal differentiation and migration. These findings determine that CTCF is required for a propriate function of the mature excitatory neurons, independent of roles during development. Significance StatementThe gene CTCF is an important regulator of gene expression. Mutations in CTCF have been identified in individuals with a range of neurodevelopmental disorders, including intellectual disability and autism. However, it is unknown if CTCF is important only for neuronal development, or plays functional roles in the brain during adulthood. The current study finds that CTCF deletion during adulthood in excitatory neurons induces a behavioral phenotype that that includes increase in anxiety and depression-like behavior and changes in social behavior. In addition, CTCF depletion in adulthood affects the morphology, identity and gene expression of these specific types of neurons. Therefore, CTCF is not only important in brain development, but also in maintenance of proper neuronal function and behavior during adulthood.

neuroscience↗

Bacteroides is increased in an autism cohort and induces autism-relevant behavioral changes in mice in a sex-dependent manner

Autism Spectrum Disorder (ASD) is a neurodevelopmental condition which is defined by decreased social communication and the presence of repetitive or stereotypic behaviors. Recent evidence has suggested that the gut-brain axis may be important in neurodevelopment in general and may play a role in ASD in particular. Here, we present a study of the gut microbiome in 96 individuals diagnosed with ASD in Israel, compared to 42 neurotypical individuals. We determined differences in alpha and beta diversity in the microbiome of individuals with ASD and demonstrated that the phylum Bacteroidetes and genus Bacteroides were the most significantly over-represented in individuals with ASD. To understand the possible functional significance of these changes, we treated newborn mice with Bacteroides fragilis at birth. B. fragilis-treated male mice displayed social behavior dysfunction, increased repetitive behaviors and gene expression dysregulation in the prefrontal cortex, while female mice did not display behavioral deficits. These findings suggest that overabundance of Bacteroides, particularly in early life, may have functional consequences for individuals with ASD.

neuroscience↗

CHD8 regulates gut epithelial cell function and affects autism-related behaviours through the gut-brain axis

Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by early onset deficits in social behavior and repetitive behavior. Chromodomain helicase DNA binding protein (CHD8) is one of the genes with the strongest association to autism. Alongside with the core symptoms of ASD, individuals with ASD are reported to have gastrointestinal (GI) problems, and a majority of individuals with CHD8 mutations display GI problems. However, the relationship between autism related genes, such as CHD8, gastrointestinal function, and autism related behaviours are yet very unclear. In the current study, we found that mice haploinsufficient for CHD8 have leaky gut, a dysregulated transcriptome in gut epithelial cells, decreased gut tuft cells and goblet cells, and an increase in microbial load. Specific deletion of CHD8 in gut epithelial cells induced an increase in anxiety-related behaviours in, a phenotype that is often observed in autism and full body knockdown of CHD8, in addition to decreased tuft cells. In addition, antibiotic treatment of CHD8 haploinsufficient mice attenuates sociability deficits. Therefore, the current study determines a pathway for autism-related GI deficits, and how these deficits may play a direct role in the development of autism-related behaviours.

neuroscience↗