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Bo, B.

Publications and source records attributed to Bo, B..

8 recordsLinked to original sources

CynoBrain: A unified high-resolution framework for cross-modal data integration for macaque brain mapping

The cynomolgus macaque is a widely used primate model in neuroscience, yet existing brain atlas resources remain limited in resolution and lack a standardized framework for integrating structural, molecular, and connectivity data within a common reference space. Here we present CynoBrain, a high-resolution multi-modal brain atlas constructed from population-averaged MRI data at 9.4 Tesla, yielding a 75 micron isotropic template with significant improvement in resolution. A co-registered whole-brain autofluorescence template resolves cytoarchitectural boundaries not visible in MRI template. Three major parcellation schemes, D99 143-area, M132 105-area, and SARM are incorporated in CynoBrain space. Spatial transcriptomic based laminar definition, reconstructed from 2D sections into volumetric common space, provides a six-layer cortical segmentation spanning the whole cortex. As a demonstration of the integrative capability of this framework, 2D retrograde tracing data is reconstructed and mapped to the Cynobrain space, enabling volumetric compilation of 2D macaque brain mapping data across subjects. An online interactive platform was constructed to allow full access to Cynobrain, establishing it as a scalable, open platform for cross-modal data integration for primate neuroscience. Overall, CynoBrain is a unified framework for cross-modal data integration for macaque brain mapping with high-resolution, multiple atlases and transcriptomic based laminar definition.

neuroscience↗

Macroscopic cerebral energy efficiency corresponds to neuron reorganization in awake and anesthetized mice

Non-invasive imaging of brain function and energy supply is crucial for diagnosing and treating brain disorders. Conventional imaging struggles to capture altered relationships between energy supply and utilization caused by brain diseases. A novel method, which can be translated to human patients, is to calculate relative power (rPWR) and relative cost (rCST) to assess cerebral energy efficiency. However, whether rPWR/rCST can track individual changes and neural activity remains unproven. Our study compared these non-invasive measures with invasive two-photon microscopy in awake and anesthetized mice. We found that rPWR/rCST distributions were similar between awake mice and humans, but changed in anesthetized mice, indicating a shift in the brains economic balance. Furthermore, changes in rPWR/rCST were linked to the reorganization of microscopic neural networks, observed with two-photon microscopy. Our work highlights the potential of rPWR/rCST for medical applications, and that neural network reorganization is linked to the brains economic balance.

neuroscience↗

Fornix and Uncinate Fasciculus Support Metacognition-Driven Cognitive Offloading

People often use external tools to offload cognitive demands associated with remembering future intentions. While previous research has established a causal role of metacognition in cognitive offloading, the neural mechanisms supporting this metacognitive control process remain unclear. To address this, we conducted a study with 34 participants using diffusion tensor imaging (DTI) to examine how white matter connectivity supports metacognition-driven cognitive offloading. Behaviorally, we replicated prior findings showing that under-confidence in internal memory predicts a bias toward using external reminders. At the neural level, we used diffusion tensor imaging to quantify fractional anisotropy (FA), a measure of microstructural integrity in white matter. We found the microstructural integrity of the superior longitudinal fasciculus (SLF) and cingulum bundle (CB) negatively predicted deviations from the optimal use of reminders. The microstructural integrity of the fornix negatively predicted participants confidence in performing the task when restricted to internal memory. Our findings reveal the microstructural organization of these fronto-temporal-parietal white-matter tracts are related to metacognition driven cognitive offloading. We discuss several aspects of metacognition driven cognitive offloading from a white matter microstructural perspective.

neuroscience↗

Cerebral Blood Volume Modulates Glymphatic Influx Through Extra-ventricular Cerebrospinal Fluid Volume

The glymphatic system facilitates waste removal via cerebrospinal fluid (CSF) influx alongside perivascular spaces throughout the brain. Vasomotion, the slow motion of blood vessel (0.1-0.3 Hz), has been found to be one of the driving forces for perivascular clearance, but it is not clear whether more chronical change of vessel diameter, as reflected by macroscopic cerebral blood volume (CBV), has any impact on glymphatic function. Combining multimodal mouse MRI techniques, we investigated the relationship among glymphatic influx, CBV, CSF volume and EEG power under six different conditions (awake, dexmedetomidine, isoflurane, isoflurane/dexmedetomidine, ketamine/xylazine and awake with caffeine). We found dexmedetomidine and caffeine enhanced glymphatic influx, while isoflurane reduced it compared with awake condition. Quantitative CBV imaging revealed that glymphatic influx was negatively correlated to CBV across the above conditions. Furthermore, such negative correlation was found to be mediated in part by changes of extra-ventricular CSF volume, which was quantified using T1 MRI. Taken together, our results suggest that CBV is a consciousness independent modulator of glymphatic function and modulates glymphatic influx through extra-ventricular CSF volume. This new finding opens potential avenues to enhance brain waste clearance by regulating CBV, which could be beneficial for protein deposition related neurological diseases. TeaserCBV is a consciousness independent modulator of glymphatic function and modulates glymphatic influx through extra-ventricular CSF volume.

neuroscience↗

Spatially resolved molecular and cellular atlas of the mouse brain

A comprehensive atlas of genes, cell types, and their spatial distribution across a whole mammalian brain is fundamental for understanding function of the brain. Here, using snRNA-seq and Stereo-seq techniques, we generated a mouse brain atlas with spatial information for 308 cell clusters with single-cell resolution involving over 6 million cells as well as for 29,655 genes. We have identified new astrocyte clusters, and demonstrated that distinct cell clusters exhibit preference for cortical subregions. In addition, we identified 155 genes exhibiting regional specificity in the brainstem, and 513 long non-coding RNA exhibited regional specificity in the adult brain. Parcellation of brain regions based on spatial transcriptomic information showed large overlap with that by traditional method. Furthermore, we have uncovered 411 transcription factor regulons with spatiotemporal specificity during development. Thus, our study has discovered genes and regulon with spatiotemporal specificity, and provided a high-resolution spatial transcriptomic atlas of the mouse brain.

neuroscience↗

Instantaneous antidepressant effect of lateral habenula deep brain stimulation in rats studied with functional magnetic resonance imaging

The available treatments for depression have substantial limitations, including low response rates and substantial lag time before a response is achieved. We applied deep brain stimulation (DBS) to the lateral habenula (LHb) of two rat models of depression (Wistar Kyoto rats and lipopolysaccharide-treated rats) and observed an immediate (within seconds to minutes) alleviation of depressive-like symptoms with a high response rate. Simultaneous functional magnetic resonance imaging (fMRI) conducted on the same sets of depressive rats used in behavioral tests revealed DBS-induced activation of multiple regions in afferent and efferent circuitry of the LHb. The activation levels of brain regions connected to the medial LHb (M-LHb) was correlated with the extent of behavioral improvements. Rats with more medial stimulation sites in the LHb exhibited greater antidepressant effects than those with more lateral stimulation sites. These results indicated that the antidromic activation of the limbic system and orthodromic activation of the monoaminergic systems connected to the M-LHb played a critical role in the rapid antidepressant effects of LHb-DBS. This study indicates that M-LHb-DBS might act as a valuable, rapid-acting antidepressant therapeutic strategy for treatment-resistant depression and demonstrates the potential of using fMRI activation of specific brain regions as biomarkers to predict and evaluate antidepressant efficacy.

neuroscience↗

A systematically optimized awake mouse fMRI paradigm

Functional magnetic resonance imaging (fMRI) has been increasingly utilized in mice. Due to the non-negligible effects of anesthetics on mouse fMRI, it is becoming more common to perform fMRI in the awake mice. However, high stress level and head motion in awake mouse fMRI remain to be fully addressed, which limits its practical applications. Therefore, here we presented a systematically optimized awake mouse fMRI paradigm as a practical and open-source solution. First, we designed a soundproof habituation chamber in which multiple mice can be habituated simultaneously and independently. Then, combining corticosterone, body weight and behavioral measurements, we systematically evaluated the potential factors that may contribute to animals stress level for awake imaging. Among many factors, we found that the restraining setup allowing forelimbs freely moving and head tilted at 30-degree was optimal for minimizing stress level. Importantly, we implemented multiband simultaneous multi-slice imaging to enable ultrafast fMRI acquisition in awake mice. Compared to conventional single-band EPI, faster acquisition enabled by multiband imaging were more robust to head motion and yielded higher statistical power. Thus, more robust resting-state functional connectivity was detected using multiband acquisition in awake mouse fMRI, compared to conventional single-band acquisition. In conclusion, we presented an awake mouse fMRI paradigm that is highly optimized in both awake mice habituation and fMRI acquisition, and such paradigm minimized animals stress level and provided more resistance to head motion and higher statistical power.

neuroscience↗

Global Mapping of Mouse CSF Flow via HEAP-METRIC Phase-contrast MRI

Roles of Cerebrospinal fluid (CSF) in brain waste clearance and homeostasis has been increasingly recognized, thus measuring its flow dynamics could provide important information about its function and perturbance. While phase-contrast MRI can be used for non-invasive flow mapping, so far its mapping of low velocity flow (such as mouse brain CSF) is not possible. Here we developed a novel generalized Hadamard encoding based multi-band acceleration scheme dubbed HEAP-METRIC (Hadamard Encoding APproach of Multi-band Excitation for short TR Imaging aCcelerating), and with significantly increased SNR per time, HEAP-METRIC phase-contrast MRI achieved fast and accurate mapping of slow (~102 micron/s) flow. Utilizing this novel method, we revealed a heterogeneous global pattern of CSF flow in the awake mouse brain with a averaged flow of ~200 micron/s, and further found isoflurane anesthesia reduced CSF flow that was accompanied by reduction of glymphatic function. Therefore, we developed the novel HEAP-METRIC phase-contrast MRI for mapping low velocity flow, and demonstrated its capability for global mapping of mouse CSF flow and its potential alterations related to various physiological or pathological conditions.

neuroscience↗