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Miyata, K.

Publications and source records attributed to Miyata, K..

15 recordsLinked to original sources

Deep learning-based prediction of wall shear stress throughout the cardiac cycle in middle cerebral artery bifurcation aneurysms

Background and Objective: Cardiac-cycle wall shear stress (WSS) is relevant to intracranial aneurysm hemodynamic assessment, but transient computational fluid dynamics (CFD) is costly. Existing surrogates use steady-flow priors or joint steady/transient training; here we evaluate the transfer of separately pretrained spatial parameters. This study develops the Steady-to-Transient Estimation of Pulsatile Wall Shear Stress (STEP) framework, a two-stage geometric learning approach for full-cycle WSS prediction. Methods: Using the synthetic AneuG-Flow dataset, Stage 0 pretrained a geometric tokenizer, LaB-GATr backbone, and WSS decoder on 11,656 steady CFD cases. Stage 1 initialized these components from the pretrained model and fine-tuned them end to end using 449 transient training cases, with 72 validation and 57 primary test cases. Waveform embeddings multiplicatively conditioned geometric features across blocks at 80 cardiac-cycle time points. Gaussian curvature was included as an auxiliary geometry feature. Ablations evaluated steady initialization, temporal conditioning, and curvature, with rank-biserial effect sizes and Holm-adjusted p values. A fixed model was also evaluated on 231 additional cases, with registered-geometry overlap audited across stages. Results: On the primary test set, STEP achieved a whole-cycle WSS vector mean absolute error (MAE) of 1.688 Pa and root-mean-square error (RMSE) of 2.877 Pa. Time-averaged WSS, oscillatory shear index, and relative residence time MAEs were 1.040 Pa, 0.00625, and 0.06734 Pa-1, respectively. Steady initialization reduced vector MAE by 27.93% relative to training the same transient architecture from scratch; the complete blockwise conditioning configuration reduced MAE by 8.04% relative to input-only additive conditioning (rank-biserial correlations 0.995 and 0.982, respectively; Holm-adjusted p < 0.001). Curvature yielded a 3.46% reduction without a significant paired effect (adjusted p = 0.0521). The 80-time-point WSS prediction required a mean of 4.169 s (SD 0.063 s). Additional-cohort MAE was 1.712 Pa, but 185/231 geometries matched Stage 0 training, versus 1/57 in the primary test set. Conclusions: STEP demonstrated effective reuse of steady-pretrained spatial parameters for cardiac-cycle WSS prediction under the evaluated synthetic CFD protocol. The strongest controlled gains were associated with steady initialization and the complete temporal-conditioning configuration. The common inlet waveform and cross-stage geometry overlap limit generalization claims.

bioengineering↗

Can carcasses cause environmental nucleic acid pollution? Implications for interpreting environmental RNA/DNA survey results

Environmental nucleic acid (eRNA and eDNA) metabarcoding is a promising tool for biodiversity assessment as it supports low-cost, noninvasive biological surveys. A critical challenge for eRNA/eDNA analyses is accounting for nucleic acid contamination that can compromise the accuracy of biomonitoring results. The primary aim of the current study was to examine carcasses as potential sources of eRNA/eDNA contamination, a contribution that remains poorly understood. Using Japanese medaka (Oryzias latipes), we quantified the detectability and persistence of carcass-derived eRNA/eDNA in water through two complementary experiments: (i) a shedding study comparing eRNA/eDNA release from live and dead individuals and (ii) a decay experiment measuring temperature-dependent degradation from 4 to 34 {degrees}C. Dead fish released detectable amounts of both eDNA and eRNA, indicating that eRNA-based surveys cannot fully eliminate carcass-derived signals. Arrhenius-based analysis showed that eRNA degradation was more temperature-dependent than eDNA degradation. These results suggest that eRNA may improve temporal resolution for recent organismal presence under warm conditions, whereas carcass-derived eRNA may persist under cold conditions and complicate interpretation of positive detections. Overall, eRNA may help reduce carcass-related false positives, particularly in warm conditions, but should be paired with temperature-aware sampling strategies and temporal replication during colder periods.

ecology↗

Identification of novel kolmioviruses in diverse invertebrates.

Kolmioviruses (KoVs; family Kolmioviridae) are circular, single-stranded RNA viruses that have recently been discovered in a wide range of animal species. However, invertebrate-associated KoVs have so far been identified only in termites and their diversity and evolution remain largely unexplored. Here, we comprehensively analyzed publicly available animal RNA-seq datasets and identified six novel KoVs associated with one fish and five invertebrate species: coho salmon (Oncorhynchus kisutch [Walbaum, 1792]), spotted babylon (Babylonia areolata [Link, 1807]), Atlantic pearl oyster (Pinctada imbricata [Roding, 1798]), small emerald moth (Hemistola chrysoprasaria [Esper, 1795]), codling moth (Cydia pomonella [Linnaeus, 1758]), and cocoa pod borer (Conopomorpha cramerella [Snellen, 1904]).

microbiology↗

HistoSB-Net: Semantic Bridging for Data-Limited Cross-Modal Histopathological Diagnosis

Vision-language models (VLMs) provide a unified framework for multimodal reasoning, yet their representations are primarily learned from natural image-text corpora and often exhibit semantic misalignment when transferred to histopathology, particularly under data-limited diagnostic settings. To address this limitation, we propose HistoSB-Net, a semantic bridging network designed to adapt pre-trained VLMs to multimodal histopathological diagnosis while preserving their original semantic structure. HistoSB-Net introduces a constrained semantic bridging (CSB) module that operates within the self-attention projection space of both vision and text encoders. Instead of employing explicit cross-attention or full fine-tuning, CSB adaptively modulates pre-trained attention projections through a lightweight nonlinear semantic bottleneck, enabling structured cross-modal regulation with limited additional parameters. The framework supports both patch-level and whole-slide image (WSI)-level diagnosis within a unified architecture. Experiments on six pathology benchmarks, comprising two WSI-level and four patch-level datasets, demonstrate consistent improvements over zero-shot inference across 36 backbone-dataset combinations under limited supervision. Further analysis of prototype-based margin distributions and confusion matrices shows that these improvements are accompanied by enhanced intra-class compactness and increased inter-class separation in the embedding space. These results indicate that CSB provides an effective and computationally manageable strategy for adapting pre-trained VLMs to data-limited digital pathology tasks.

pathology↗

Metabolic reprogramming and stress mitigation of Chlamydomonas reinhardtii using protective metal-phenolic networks

Single-cell encapsulation is widely used in biotechnology to protect highly sensitive living cells from environmental stress. However, the impact of encapsulation on biological function and metabolism remains rarely explored despite its importance for understanding stress response and modulating the production of valuable metabolites. Herein, we show that coating individual cells with protective metal-phenolic networks not only improves survival against stress, but also modifies cellular metabolism. Importantly, this encapsulation technique induces a reversible state of quiescence, which enables accumulation of high-energy-density compounds through selective nutrient diffusion and the resulting carbon flux redistribution. Specifically, light exposure favors the accumulation of nearly eightfold higher starches, while incubation in darkness leads to twofold higher lipid accumulation compared to native cells. This metabolic engineering approach via individual cell encapsulation expands the cell editing toolbox and will facilitate applications in synthetic biology, bioengineering, and cell-based therapeutics. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=184 SRC="FIGDIR/small/711231v2_ufig1.gif" ALT="Figure 1"> View larger version (60K): org.highwire.dtl.DTLVardef@d27478org.highwire.dtl.DTLVardef@dc73baorg.highwire.dtl.DTLVardef@131dcaeorg.highwire.dtl.DTLVardef@8f3dc4_HPS_FORMAT_FIGEXP M_FIG C_FIG

bioengineering↗

Plasticity of extrachromosomal DNA segregation during drug adaptation

Uneven segregation during mitosis is a striking feature of extrachromosomal DNA (ecDNA). Because ecDNA lacks a centromere, it is thought to segregate stochastically and randomly during cell division, thereby generating extensive intratumoral heterogeneity in genomic copy number. Several studies have reported that ecDNA copy numbers can readily change in response to drug treatment, which enables the cells to acquire drug resistance. However, the mechanisms underlying these dynamic changes remain poorly understood --particularly whether such copy-number changes result from static selection of pre-existing clones or from active reconfiguration under drug-induced stress. This key question remains unresolved, mainly due to the absence of technologies capable of tracking ecDNA copy number simultaneously across clones. To overcome this limitation, we developed a high-throughput framework that combines single-cell DNA sequencing with cellular barcoding for clonal tracking of ecDNA copy-number dynamics. The results of single-cell cloning experiments revealed that not all clones exhibit identical segregation modes even under drug-free conditions. Clonal tracking under drug treatment showed that resistant populations do not simply emerge from pre-existing clones with favorable ecDNA states; instead, some clones seemed capable of actively reconfiguring their segregation behavior, possibly involving neuron-like alternation in microtubule organization and intracellular transport pathways, to generate drug-resistant cells. These findings suggest that, although ecDNA might segregate stochastically, it may undergo nonrandom, actively regulated segregation under drug stress. This discovery allows the therapeutically targeting of ecDNA segregation mechanisms to counteract adaptive drug resistance.

cell biology↗

Environmental RNA/DNA Metabarcoding for Ecological Risk Assessment of Chemicals Based on Response of Benthic Communities in Natural Environments

To achieve the current Nature Positive goals, it is important to identify the effects of chemicals on ecosystems and strategically reduce their risks. We therefore estimated the safe concentration (SC) of linear alkylbenzene sulfonate (LAS) by investigating the relationship between benthic communities detected via environmental RNA (eRNA) and environmental DNA (eDNA) metabarcoding and the water quality in a river contaminated with LAS. Non-metric multidimensional scaling of benthic communities detected via eRNA indicated significant differences between contaminated and non-contaminated sites, and redundancy analysis showed significant correlation between the benthic communities and LAS concentration. These results demonstrate that eRNA is more sensitive than eDNA for capturing the community changes that result from LAS contamination. No significant differences were observed in biodiversity indices between the highest LAS concentration site and non-contaminated site; thus, the SC was estimated at >47 {micro}g/L. The results suggest that, although hazard assessment using the assessment factor (AF) leads to conservative estimation of the effects of chemicals because the predicted no-effect concentration in previous studies is lower than the SC, hazard assessment based on the response of biological communities using eRNA metabarcoding can refine such ecological assessments, developing the environmental management standards to achieve nature-positive goals.

ecology↗

Clonal lineage tracing and parallel multiomics profiling reveal transcriptional diversification induced by ARID1A deficiency

Phenotypic heterogeneity among genetically identical cancer cells underpins tumor progression and therapy resistance. However, the mechanism of epigenetic dysregulation that drives such divergence remains unclear. This study introduces integrated multimodal experimental platform specialized in analyzing inter/intraclonal heterogeneity (IMPACH), a scalable platform that integrates lineage tracing, genetic perturbation, and multimodal single-cell analysis. Utilizing IMPACH, results revealed that loss of epigenetic regulators--particularly ARID1A--enhances transcriptomic and epigenetic heterogeneity under controlled conditions. ARID1A deficiency promotes stochastic chromatin opening and induces an atypical gene expression program associated with poor clinical outcomes. Despite increased epigenetic randomness, chromatin changes remain localized to regulatory elements, partially linked to SMARCA4 binding sites. These findings revealed that chromatin remodeling defects promote clonal diversification through both stochastic and constrained mechanisms. Thus, owing to its scalability and versatility, IMPACH provides a robust framework for elucidating how epigenetic perturbations shape cellular heterogeneity in cancer.

cancer biology↗

Probing nanomechanics by direct indentation using Nanoendoscopy-AFM reveals the nuclear elasticity transition in cancer cells

The assessment of nuclear structural changes is considered a potential biomarker of metastatic cancer. However, accurately measuring nuclear elasticity remains challenging. Traditionally, nuclear elasticity has been measured by indenting the cell membrane with a bead-attached atomic force microscopy (AFM) probe or aspirating isolated nuclei with a micropipette tip. However, indentation using a bead-attached probe is influenced by the cell membrane and cytoskeleton, while measurements of isolated nuclei do not reflect their intact state. In this study, we used Nanoendoscopy-AFM, a technique in which a nanoneedle probe is inserted into a living cell to directly measure nuclear elasticity and map its distribution. Our findings show that nuclear elasticity increases under serum depletion but decreases when serum-depleted cells are treated with TGF-{beta}, which induces epithelial-mesenchymal transition (EMT). Furthermore, we found that changes in nuclear elasticity correlate positively with trimethylation levels of histone H4 at lysine 20, rather than with nuclear lamins expression levels. These findings suggest that alterations in chromatin structure underlie changes in nuclear elasticity during cancer progression.

biophysics↗

Cholesterol sulfate prevents maternal-fetal conflict by locally modulating immune reactivity

Although placental mammals are at high risk of maternal-fetal immune conflict, it is unclear how the semi-allogeneic fetus avoids rejection. Cholesterol sulfate (CS) is a bioactive metabolite that inhibits leukocyte migration and activation. This study investigated the roles and cells associated with CS in pregnant mice and humans. CS was sequentially produced by maternal-derived endometrial cells and fetal-derived placental trophoblasts before and after placentation. When mated with allogeneic males, CS-deficient mice showed increased fetal resorption rates under induced placental inflammation. This phenotype disappeared when the activity of the CS-producing enzyme was restored in the placenta. Placental CS levels were reduced in patients with "villitis of unknown etiology." Thus, we uncovered the spatiotemporal control of CS production and its relevance to local immunosuppression during pregnancy.

immunology↗

Fish environmental RNA sequencing sensitively captures accumulative stress responses through short-term aquarium sampling

The utility of environmental RNA (eRNA) in capturing biological responses to stresses has been discussed previously; however, the limited number of genes detected remains a significant hindrance to its widespread implementation. Here, we investigated the potential of eRNA to assess the health status of Japanese medaka fish exposed to linear alkylbenzene sulfonate. Analyzing eRNA and organismal RNA (oRNA) in aquarium water for > 12 h, we achieved high mapping rates and 10 times more differentially expressed genes than previously reported. This advancement has facilitated the previously unattainable capability of gene ontology (GO) analysis. In GO analysis, it was found that eRNA could detect nuclear genes in cellular component, and oRNA provided gene expression signatures in the short term, whereas eRNA demonstrated the potential to reflect cumulative gene expression signatures over a period of time in biological process. Moreover, eRNA exhibited high sensitivity in responding to genes associated with sphingolipid and ceramide biosynthesis, which are involved in inflammatory responses possibly originating from impaired cells. This finding aligns with the observations made in oRNA. Conclusively, eRNA-sequencing (eRNA-seq) using aquarium water emerges as a valuable high sensitivity tool for analyzing physiological stress. The findings of this study lay the foundation for further development of eRNA-seq technologies.

ecology↗

Deciphering mechanisms of UV filter- and temperature-induced bleaching in the coral Acropora tenuis, using ecotoxicogenomics

Coral reefs are at risk of bleaching due to various environmental and anthropogenic stressors such as global warming and chemical pollutants. However, there is little understanding of stressor-specific mechanisms that cause coral bleaching. Therefore, conducting accurate ecotoxicological risk assessments and deciphering modes of action of potentially deleterious ultraviolet (UV) filters (sunscreen compounds) are crucial issues. In this study, we evaluated the toxicity and bleaching effect of benzophenone-3 (BP-3), which is widely used in sunscreen products, on the reef-building coral Acropora tenuis. Furthermore, to understand differences in UV filter- and temperature-induced bleaching, a comparative ecotoxicogenomic approach using RNA-seq was integrated into a toxicity test to clarify differences in gene expression changes induced by BP-3 and heat stress (31{degrees}C). The lethal concentration 50% (LC50) was calculated as 3.9 mg/L, indicating that emission level of BP-3 was properly controlled based on the risk assessment. Differentially expressed genes related to oxidative stress and extracellular matrix organization were involved in coral responses to both BP-3 and heat stress, but their patterns differed. Whereas immune and heat-shock responses were activated in response to heat stress, activation of a drug metabolism pathway and several signal transduction pathways were identified in BP-3 treatment groups. Our study enhances understanding of stress responses in corals induced by UV filters and thermal stress. Using potential gene markers identified in this study for eco-epidemiological surveys of stressed corals, we urgently need to develop effective countermeasures.

ecology↗

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↗

The tRNA pseudouridine synthase TruB1 regulates the maturation and function of let-7 miRNA

Let-7 is an evolutionary conserved microRNA that mediates post-transcriptional gene silencing to regulate a wide range of biological processes, including development, differentiation, and tumor suppression. Let-7 biogenesis is tightly regulated by several RNA-binding proteins, including Lin28A/B, which represses let-7 maturation. To identify new regulators of let-7, we devised a cell-based functional screen of RNA-binding proteins using a let-7 sensor luciferase reporter, and identified the tRNA pseudouridine synthase, TruB1. TruB1 enhanced maturation specifically of let-7 family members. Rather than inducing pseudouridylation of the miRNAs, HITS-CLIP (High throughput sequencing crosslinking immunoprecipitation) and biochemical analyses revealed direct binding between endogenous TruB1 and the stem-loop structure of pri-let-7, which also binds Lin28A/B. TruB1 selectively enhanced the interaction between pri-let-7 and the microprocessor DGCR-8, which mediates miRNA maturation. Finally, TruB1 suppressed cell proliferation, which was mediated in part by let-7. Altogether, we reveal an unexpected function for TruB1 in promoting let-7 maturation and function.

molecular biology↗

Parallel loss of symbiosis genes in relatives of nitrogen-fixing non-legume Parasponia

Rhizobium nitrogen-fixing nodules are a well-known trait of legumes, but nodules also occur in other plant lineages either with rhizobium or the actinomycete Frankia as microsymbiont. The widely accepted hypothesis is that nodulation evolved independently multiple times, with only a few losses. However, insight in the evolutionary trajectory of nodulation is lacking. We conducted comparative studies using Parasponia (Cannabaceae), the only non-legume able to establish nitrogen fixing nodules with rhizobium. This revealed that Parasponia and legumes utilize a large set of orthologous symbiosis genes. Comparing genomes of Parasponia and its non-nodulating relative Trema did not reveal specific gene duplications that could explain a recent gain of nodulation in Parasponia. Rather, Trema and other non-nodulating species in the Order Rosales show evidence of pseudogenization or loss of key symbiosis genes. This demonstrates that these species have lost the potential to nodulate. This finding challenges a long-standing hypothesis on evolution of nitrogen-fixing symbioses, and has profound implications for translational approaches aimed at engineering nitrogen-fixing nodules in crop plants.

plant biology↗