The hippocampus, including the dorsal dentate gyrus (dDG), and cortex engage in bidirectional communication. We propose that low-frequency activity in hippocampal-cortical pathways contributes to brain-wide resting-state connectivity to integrate sensory information. Using optogenetic stimulation and brain-wide fMRI and resting-state fMRI (rsfMRI), we determined the large-scale effects of spatiotemporal-specific downstream propagation of hippocampal activity. Low-frequency (1 Hz), but not high-frequency (40 Hz), stimulation of dDG excitatory neurons evoked robust cortical and subcortical brain-wide fMRI responses. More importantly, it enhanced interhemispheric rsfMRI connectivity in various cortices and hippocampus. Subsequent local field potential recordings revealed an increase in slow oscillations in dorsal hippocampus and visual cortex, interhemispheric visual cortical connectivity, and hippocampal-cortical connectivity. Meanwhile, pharmacological inactivation of dDG neurons decreased interhemispheric rsfMRI connectivity. Functionally, visually evoked fMRI responses in visual regions also increased during and after low-frequency dDG stimulation. Together, our results indicate that low-frequency activity robustly propagates in the dorsal hippocampal-cortical pathway, drives interhemispheric cortical rsfMRI connectivity, and mediates visual processing.hippocampus | resting-state functional connectivity | optogenetic | fMRI | low frequency T he hippocampus (HP) plays a prominent role in central nervous system functions, particularly in episodic memory (1, 2) and spatial navigation (3, 4). The HP, including the dentate gyrus (DG), can evoke large-scale influences on cortical activity, because the HP receives convergent information from sensory and limbic cortices before sending reciprocal divergent projections to create a highly interactive corticohippocampal-cortical network. The HP, including DG, CA3, and CA1, and neocortex, are connected via the entorhinal cortex (EC) (5, 6), such that the dorsolateral-to-ventromedial projection that originates in the EC corresponds to a dorsoventral axis of termination in the HP (5). This anatomical topography suggests that a functional gradient could exist along the HP dorsoventral axis. Previous studies demonstrated that dorsal HP (dHP) and cortex are functionally integrated during sensory processing and memory consolidation (7-9). Specifically, dHP can integrate multimodal sensory information and process memory operations (7) using excitatory longrange projections (10). This process occurs over multiple brain circuits, but the role of dHP in complex networks, particularly its influence on brain-wide functional connectivity, is not well understood.Resting-state functional MRI (rsfMRI) (11-14) provides an invaluable, noninvasive imaging technique to map long-range, brain-wide functional connectivity networks based on the temporal coherence of infraslow (0.005-0.1 Hz) blood oxygen level dependent (BOLD) activity. The functional relevance of specific brain-wide networks in co...
Treatment with a single injection of anti‐CD40L (CD154) monoclonal antibody (mAb) and fully mismatched allogeneic bone marrow transplant (BMT) allows rapid tolerization of CD4+ T cells to the donor. The addition of in vivo CD8 T‐cell depletion leads to permanent mixed hematopoietic chimerism and tolerance. We now describe two approaches that obviate the requirement for CD8 T‐cell depletion by rapidly tolerizing recipient CD8 T cells in addition to CD4 cells. Administration of donor‐specific transfusion (DST) to mice receiving 3 Gy total body irradiation (TBI), BMT and anti‐CD40L mAb on day 0 uniformly led to permanent mixed chimerism and tolerance, compared with only 40% of mice receiving similar treatment without DST. In the absence of DST, moving the timing of 3 Gy TBI to day –1 or day –2 instead of day 0 led to rapid (by 2 weeks) induction of CD8+ cell tolerance, and also permitted uniform achievement of permanent mixed chimerism and donor‐specific tolerance in recipients of anti‐CD40L and BMT on day 0. These nontoxic regimens overcome CD8+ and CD4+ T‐cell‐mediated alloresistance without requiring host T‐cell depletion, permitting the induction of permanent mixed chimerism and tolerance.
Magic angle-enhanced MRI can detect ocular fibrous microstructures without contrast agents or coatings and can reveal their MR tissue property changes with IOP loading. This technique may open up new avenues for assessment of the biomechanical and biochemical properties of ocular tissues in aging and in diseases involving the corneoscleral shell.
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