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Biology subjects

Motomura, Y.

Publications and source records attributed to Motomura, Y..

3 recordsLinked to original sources

Early-stage neural processing reveals distinctive responses to saliency-differentiated colors in various types of color vision

Individuals with minority color vision phenotypes have been reported to exhibit enhanced color discrimination and color recognition, which deviate from predictions based on their receptoral sensitivities. However, the specific mechanisms underlying this enhanced sensitivity remain unclear. In this study, we examined the commonality and diversity of neural activity between typical and anomalous trichromats in response to differences in color saliency. Electroencephalography was recorded during an oddball task, in which participants discriminated each of two target stimuli, blue-green and red, from a green standard stimulus. The chromaticity of the stimulus was identical across participants, whereas the relationship of saliency between the target stimuli was expected to be reversed between color vision types. The spatiotemporal dynamics of event-related potentials (ERPs) were analyzed using cluster-based permutation tests. Typical trichromats demonstrated faster behavioral and neural responses to the more salient red target stimulus, with pronounced neural activity spreading from the occipital to the parietal regions in the comparison between the target stimuli. Anomalous trichromats also exhibited similar temporal patterns toward the more salient target stimulus when each target stimulus was compared with the green standard stimulus, indicating comparable processing toward saliency across color vision types. Although a similarity was observed, neither behavioral nor neural responses in anomalous trichromats reflected saliency contrast differences. In addition, a comparative analysis of ERPs between color vision types did not reveal any distinct differences in either target stimulus. Given the large variations in color sensitivity in individuals with anomalous trichromacy, further investigation is required to understand the detailed neural processing in individuals with various color vision types.

neuroscience↗

NFκB nuclear dynamics orchestrate inflammatory aging

Upregulation of nuclear factor {kappa}B (NF{kappa}B) signaling is a hallmark of aging and major cause of age-related chronic inflammation; however, its physiological functions and mechanisms remain unclear. By combining mathematical modeling and experiments, we show that dysfunction of negative feedback regulators of NF{kappa}B, I{kappa}B and A20, alters the NF{kappa}B nuclear dynamics from oscillatory to sustained, promoting cellular senescence by remodeling epigenetic regulation and metabolic landscape. Sustained NF{kappa}B activity by I{kappa}B downregulation enhanced inflammation- and senescence-associated gene expression through increased NF{kappa}B-DNA binding and slowed the cell cycle by upregulating purine catabolism via mTORC2/AKT pathways. Notably, I{kappa}B knockdown combined with A20 overexpression resulted in lower NF{kappa}B amplitude, cytokine expression, and SA-{beta}-gal activity than I{kappa}B knockdown alone. I{kappa}B downregulation is correlated with hypoxanthine phosphoribosyltransferase 1 (HPRT1) expression in the purine salvage pathway in aged mouse hearts. Our study suggests that nuclear NF{kappa}B homeostasis is critical for balancing purine metabolism associated with chronic inflammation and tissue aging.

systems biology↗

Quantitative live-cell imaging of secretion activity reveals dynamic immune responses

The measurement of cytokine secretions has contributed to the development of immunology; however, new methods that enable highly sensitive and efficient analysis are required for the precise characterisation of dynamic secretion activity when using rare cells or limited human specimens. Here, we report a new technology for quantitative live-cell imaging of secretion activity (qLCI-S), that enables high-throughput and dual-colour detection of prolonged secretion activity at the single-cell level, followed by transcriptome analysis for individual cells based on their phenotype. The power of the qLCI-S was demonstrated by visualising the individual and longitudinal cytokine secretion patterns of group 2 innate lymphoid cells, which comprised <0.01% human peripheral blood mononuclear cells, and identifying their minor subpopulations. This new technology will provide new insights into the spatiotemporal dynamic nature of various secretory functions and the development of fundamental tools for phenotypic drug discovery and regenerative and precision medicine.

biophysics↗