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Hardin, E. J.

Publications and source records attributed to Hardin, E. J..

3 recordsLinked to original sources

ALS/FTD-linked TDP-43 alterations prevent HSV-1 infection by disrupting cell-adhesion pathways

TAR DNA-binding protein-43 (TDP-43) alterations are a key hallmark of amyotrophic lateral sclerosis (ALS), frontotemporal dementia (FTD), and other neurodegenerative disorders. Increasing evidence links these conditions to viral infections, but it is not known if and how viral pathogens may be affected by disease-associated TDP-43. We found that ALS/FTD-linked forms of human TDP-43 prevent infection by herpes simplex virus type-1 (HSV-1), a common neurotropic virus. This cell-autonomous protective effect was conserved across different TDP-43 mutations, sporadic ALS, and C9ORF72-ALS, in neural and non-neural cell types, and in patient-derived cells and animal models. In addition to restricting infection, TDP-43 mutation prevented inflammatory and cell stress-related responses to HSV-1 exposure. TDP-43 knockdown but not overexpression was sufficient to protect cells from HSV-1 infection, implicating a loss-of-function mechanism. Neurons with TDP-43 mutation had disruptions in adhesion-related pathways and, accordingly, had reduced early-stage viral binding and entry. Further analyses revealed alternative RNA splicing and impairment of focal adhesion kinase (FAK/PTK2), a key mediator of cell-adhesion pathways. Inhibition of FAK was sufficient to decrease HSV-1 infection, and genetic enhancement of functional but not inactive FAK promoted infectivity in cells with TDP-43 mutation. Together, these data indicate that TDP-43 affects virus-host interactions by influencing adhesion pathways required for viral infection.

neuroscience↗

δ-catenin controls layer-specific transcriptional maturation of astrocytes via Zbtb20

Coordinated maturation of diverse neural cell types drives mammalian cortical circuit development. Disruption of this coordination is a hallmark of human neurodevelopmental disorders, yet mechanisms that synchronize transcriptional maturation across cell types remain poorly understood. Here, we identify {delta}-catenin (Ctnnd2), a component of adherens junctions, that links cell-cell interactions to transcriptional regulation. Using single-nucleus and spatial transcriptomics, we show that {delta}-catenin loss disrupts transcriptional maturation across neural cell types, particularly in astrocytes. {delta}-catenin loss impairs acquisition of layer-specific astrocyte identities and prolongs ocular dominance plasticity, indicating impaired circuit stabilization. Mechanistically, we identify the BTB/POZ transcription factor Zbtb20, which is enriched in glial cells, as a key regulator of this process. {delta}-catenin loss increases Zbtb20 expression, redistributes its genome-wide binding, and dysregulates its target genes. Together, these findings support a model in which {delta}-catenin regulates Zbtb20-dependent transcriptional programs to establish layer-specific astrocyte identities in coordination with developing cortical circuits. SUMMARYSejourne et al report that loss of the adherens junction protein {delta}-catenin prolongs ocular dominance plasticity and disrupts astrocyte and oligodendrocyte transcriptional identity. The underlying mechanism seems to rely on the glia-enriched transcription factor Zbtb20, which is upregulated and redistributed upon {delta}-catenin loss, resulting in altered expression of its target genes.

cell biology↗

Brain-wide mapping of neuroanatomical connections to the auditory cortex of hearing and deaf mice

Remarkable therapeutic innovations have made it possible to establish hearing in congenitally deaf subjects. Despite these advances, a potential obstacle to restoring auditory function is that the absence of auditory experience alters the connectivity of the auditory cortex, a region that contributes to auditory perception and cognition. Here we used an intersectional genetic approach to map the brainwide inputs to the primary auditory cortex of congenitally deaf mice and their hearing littermates. We found that deaf mice displayed a significant reduction in afferents arising from the basomedial amygdala, the core of the medial geniculate nucleus, and anterior auditory thalamic nuclei. Nonetheless, major aspects of auditory cortical connectivity, including input from other thalamic nuclei and from non-auditory regions of the cortex, were unaffected by deafness. These findings highlight altered and preserved connectivity of the auditory cortex in the absence of auditory experience, which may inform therapies designed to establish hearing in congenitally deaf subjects.

neuroscience↗