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Biology subjects

Kabe, Y.

Publications and source records attributed to Kabe, Y..

2 recordsLinked to original sources

Delineating neural contributions to electroencephalogram-based speech decoding

Speech Brain-computer interfaces (BCIs) have emerged as a pivotal technology in facilitating communication for individuals with speech impairments. Utilizing electroencephalography (EEG) for noninvasive speech BCIs offers an accessible and affordable solution, potentially benefiting a broader audience. However, EEG-based speech decoding remains controversial especially for overt speech, due to difficulties in separating speech-related neural activities from myoelectric potential artifacts generated during articulation. Here we aim to delineate the extent of the neural contributions by employing Explainable AI techniques to a convolutional neural network predicting spoken words based on signals obtained by ultra-high-density (uhd)-EEG. We found that electrode-wise contributions to the decoding cannot be explained by their mutual information with electromyography (EMG). Furthermore, contributing periods of speech to EEG-based decoding are distinct from those to decoding solely relying on EMG. In contrast, there are significant overlaps in signal timings contributing to EEG-based decoding, regardless of vocal conditions such as overt or covert speech. Notably, the denoising process successfully enhanced the decoding contribution from electrodes within speech-related brain areas for all speech conditions. Altogether, our findings support the idea that, with appropriate preprocessing, EEG becomes a valuable tool for decoding spoken words based on underlying neural activities.

neuroscience↗

Environmental Optimization Enables Maintenance of Quiescent Hematopoietic Stem Cells Ex Vivo

Hematopoietic stem cells (HSCs) maintain lifelong hematopoiesis by remaining quiescent in the bone marrow niche. Recapitulation of a quiescent state in culture has not been achieved, as cells rapidly proliferate and differentiate in vitro. After exhaustive analysis of different environmental factor combinations and concentrations as a way to mimic physiological conditions, we were able to maintain engraftable quiescent HSCs for 1 month in culture under very low cytokine concentrations, hypoxia, and very high fatty acid levels. Exogenous fatty acids were required likely due to suppression of intrinsic fatty acid synthesis by hypoxia and low cytokine conditions. By contrast, high cytokine concentrations or normoxia induced HSC proliferation and differentiation. Our novel culture system provides a means to evaluate properties of steady state HSCs and test effects of defined factors in vitro under near-physiological conditions.

cell biology↗