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Laliberte, G.

Publications and source records attributed to Laliberte, G..

3 recordsLinked to original sources

Projection-dependent VGluT1 and VGluT2 expression and terminal morphology in mouse visual circuits

Vesicular glutamate transporters 1 and 2 (VGluT1 and VGluT2) exhibit largely complementary distributions and have been proposed as molecular markers of descending modulatory and ascending driver-like pathways, respectively. However, this correspondence has rarely been tested directly in anatomically identified projections. We combined anterograde Phaseolus vulgaris leucoagglutinin tracing with simultaneous VGluT1 and VGluT2 immunofluorescence to characterize glutamatergic boutons arising from the primary and secondary visual cortices, lateral geniculate nucleus, lateral posterior thalamic nucleus, and superior colliculus in adult mice. Among 2,178 singly labelled boutons, VGluT1 predominated in corticothalamic, corticopontine, corticotectal, corticostriatal, and corticocortical feedback projections. Conversely, thalamocortical, tectothalamic, thalamostriatal, and tectopontine projections were almost exclusively VGluT2-positive. Projection direction did not fully predict transporter phenotype: ascending corticocortical projections remained predominantly VGluT1-positive, whereas the descending tectopontine projection was exclusively VGluT2-positive. Only 12 of 2,190 VGluT-immunoreactive boutons exhibited detectable VGluT1/VGluT2 colocalization. Morphometric analyses further revealed an interaction between VGluT isoform and projection direction. Within ascending projections, VGluT2-positive boutons and puncta were larger than their VGluT1-positive counterparts, whereas no isoform-related difference in bouton area was detected within descending projections. These findings demonstrate an association between VGluT phenotype and projection class in the mouse visual system. VGluT isoforms therefore provide informative markers of pathway organization, but neither transporter identity nor terminal size alone constitutes an invariant molecular indicator of projection direction or driver-modulator function.

neuroscience↗

Dissecting Resting-State Plasticity: Mesoscale Calcium Imaging of Excitatory and Inhibitory Neuronal Population Network Reorganization in Early Blind Mice

Early visual deprivation profoundly reshapes cortical functional organization, yet the contribution of distinct neuronal populations to large-scale network plasticity remains unclear. We combined awake wide-field mesoscale calcium imaging withing promoter-defined neuronal populations to characterize resting-state functional connectivity in pan-neuronal (hSyn), excitatory (Thy1), and inhibitory (mDLX) cortical networks in sighted and neonatal enucleated mice. Graph-theoretical analyses revealed a convergent reorganization pattern across populations in which medial higher visual and associative cortices strengthened their connectivity with somatosensory and motor regions, whereas primary visual cortex and lateral higher visual areas lost network influence. Despite this shared motif, network remodeling differed according to neuronal identity. Excitatory networks exhibited pronounced redistribution of nodal influence and modular organization with selective alterations of global network topology, indicating selective susceptibility to sensory deprivation. Inhibitory networks preserved global efficiency while showing localized reorganization of connector and bridging hubs. Pan-neuronal networks displayed extensive redistribution of connectivity and hub architecture despite relatively preserved global network organization. These findings demonstrate that early blindness induces coordinated yet neuronal identity-dependent mesoscale network plasticity, linking mouse cortical dynamics with systems-level evidence of cross-modal reorganization in blind individuals.

neuroscience↗

Cortical Functional Connectivity in Mouse Models of Early Blindness: Enucleation vs. Anophthalmia

Early sensory deprivation drives large-scale reconfiguration of cortical networks, yet we still lack a clear understanding of the relative contributions of early visual experience versus spontaneous prenatal retinal waves on the establishment of the cortical network. We compared two mouse models of congenital blindness: neonatal enucleation and congenital anophthalmia, across two genetic strains (C57Bl/6J and ZRDBA) using mesoscopic calcium imaging of spontaneous activity and graph-theoretical analysis. Spectral analyses revealed localized strain-specific increases in infraslow and low delta power following visual deprivation, with C57Bl/6J enucleated and ZRDBA anophthalmic mice exhibiting a more generalized nodal increase. Concomitantly, the functional network organization was redirected toward medial higher-order visual areas, the associative retrosplenial cortex, and somatosensory regions, while the primary and lateral visual cortices exhibited reduced influence and integration within the modular architecture. Notably, ZRDBA groups showed limited global changes to their cortical network. However, anophthalmic ZRDBA mice, lacking prenatal retinal waves, exhibited connectivity patterns more akin to enucleated C57Bl/6J than to their enucleated littermates, highlighting the instructive role of spontaneous prenatal retinal activity. These findings support a connectivity-constrained, experience-dependent model in which preexisting structural pathways guide diffuse, resilient reorganization following sensory loss.

neuroscience↗