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Hayashi, S.

Publications and source records attributed to Hayashi, S..

At least 19 recordsLinked to original sources

Probabilistic coupling of cellular and microenvironmental heterogeneity by masked self-supervised learning

AO_SCPLOWBSTRACTC_SCPLOWSpatial omics technologies have advanced to single-cell resolution, enabling systematic analysis of tissue microenvironments alongside cellular-state heterogeneity. However, computationally defining microenvironmental states at single-cell resolution and identifying representations most informative for biological discovery remain major challenges. Here we present Mievformer, a Transformer-based masked self-supervised framework that learns microenvironmental embeddings by encoding neighboring cellular states and relative spatial configurations to parameterize the conditional distribution of continuous cell states at central spatial positions. Through InfoNCE optimization, Mievformer learns representations that capture the relative enrichment of cell states across microenvironments, formalized as a conditional density ratio, thereby enabling probabilistic inference of the coupling between microenvironmental and cellular heterogeneity. Mievformer outperformed existing methods in niche clustering on simulated spatial transcriptomics data and achieved the highest average performance across five real datasets spanning three spatial transcriptomics platforms when evaluated using DREC, a ground-truth-free metric that most strongly correlated with ground-truth performance in simulations. Beyond conventional clustering, Mievformer enables identification of cellular subpopulations based on their microenvironmental distribution and detection of gene-expression signatures associated with colocalization of specific cell populations. Together, these results establish Mievformer as a quantitatively robust and biologically informative framework for learning microenvironment representations in spatial omics.

bioinformatics↗

Closed-Loop Multi-Objective Optimization for Receptor-Selective Cell-Penetrating Peptide Design

Cell-penetrating peptides (CPPs) can deliver diverse cargos into cells. However, designing CPPs with receptor-selective interaction profiles remains difficult because interactions with individual cell-surface components cannot be tuned independently. Here, we developed a closed-loop in silico framework for receptor-selective CPP design, in which receptor interactions are formulated as explicit objectives in a multi-objective optimization problem. We first constructed a CPP-like candidate library using a sequence generative model fine-tuned on known CPPs. The framework then evaluated candidate peptides by receptor-wise docking, molecular dynamics simulations, and MM/GBSA to compute receptor-wise binding scores. These scores were used iteratively to propose subsequent candidates by multi-objective Bayesian optimization. Applied to a CXCR4/NRP1 design setting, the framework identified candidates with more favorable predicted interaction profiles, characterized by higher CXCR4 binding scores and lower NRP1 binding scores. We selected 10 peptides from the computationally identified candidates for cell-based imaging and found that 4 showed higher enrichment in CXCR4-positive regions than in NRP1-positive regions under the tested conditions. These results show that the proposed framework provides a practical in silico approach for designing CPPs with receptor-selective interaction profiles.

bioinformatics↗

A cyanobacterial adenine prenyltransferase enables longer-chain N6 prenylation

Adenine, a ubiquitous nucleobase found in biomolecules such as nucleic acids, cofactors, and signaling molecules, mediates diverse molecular interactions. Here, we identify TvAPT, an adenine prenyltransferase from the cyanobacterium Trichormus variabilis NIES-23. TvAPT efficiently catalyzes the unprecedented N6-prenylation of adenine-containing substrates using extended C10 and C15 prenyl donors, whereas canonical adenine prenyltransferases are generally limited to C5-dimethylallylation. X-ray structural analyses and protein engineering revealed that an enlarged prenyl-binding pocket enables the accommodation of extended prenyl donors, providing a structural basis for rationally tuning prenyl-donor preference. Together, these findings establish TvAPT as an adenine prenyltransferase that accepts a range of adenine-containing substrates, with a preference for nucleoside 5-monophosphates. Beyond expanding the known catalytic scope of adenine prenyltransferases, TvAPT provides access to nucleotide derivatives with enhanced membrane permeability and analogues of plant signaling molecules.

biochemistry↗

Multi-Omics Mapping of Human Kidney Reveals Complement-Mediated Cellular Dynamics During Progression of Focal Segmental Glomerulosclerosis

Focal segmental glomerulosclerosis (FSGS) is a major cause of glucocorticoid-resistant nephrosis, yet its pathogenesis remains unclear. To define the molecular and cellular landscape of FSGS, we employed multi-omics approaches on independent human kidney biopsy cohorts. Proteomics revealed enhanced immune and complement activation. Spatial transcriptomics using a target gene panel constructed from the proteomics highlighted alternative pathway activation driven by complement factor D as a prominent feature. Complement activation emerged in glomeruli alongside altered signaling in podocytes and parietal epithelial cells (PECs): Podocytes displayed reduced PECAM1 and elevated macrophage migration inhibitory factor (MIF) signaling, and PECs display complement and collagen signaling as early events, and progressively acquired cellular activation, prompting glomerular fibrosis. These pathogenic signals propagated into adjacent interstitial regions, paralleling immune cell infiltration and fibrosis. These results uncover dynamics of dysregulated intercellular interactions originated from podocyte and PECs underlying the pathogenesis of FSGS, which provides insights into potential stage-specific interventions.

systems biology↗

Radiocesium Uptake in Two Fungal Bed-cultivated Edible Mushroom Species in Forests in Fukushima, Japan

In Japan, mushrooms have long been valued as food resources, but the Fukushima nuclear accident disrupted production and shipment due to radiocesium contamination. Limited knowledge has particularly hindered outdoor fungal bed cultivation. To address this, we conducted cultivation experiments with Lyophyllum decastes and Lepista nuda across 14 broad-leaved deciduous forest sites in Fukushima Prefecture. Air dose rates at 1 m height ranged from 0.04 to 0.89 {micro}Sv/h. Radiocesium concentrations (combined 137Cs and 134Cs, expressed as Bq/kg at 90% water content) in fruit bodies were 0.4-12 (mean 2.3) for Ly. decastes and 0.2-43 (mean 8.1) for Le. nuda. Both species remained below Japans food safety threshold of 100 Bq/kg, indicating that safe cultivation is feasible across broad areas. Uptake patterns differed: concentrations in Ly. decastes correlated with contamination in litter and multiple soil layers, whereas in Le. nuda it correlated only with litter contamination. These findings suggest that clean soil fills for Ly. decastes and clean litter covers for Le. nuda could serve as mitigation strategies tailored to each species. Aggregated transfer factors (2.76 x 10-5 m2/kg for Ly. decastes and 6.60 x 10-5 m2/kg for Le. nuda) were lower than those reported for wild mushrooms. Overall, this study provides new insights into reducing radiocesium assimilation by cultivated mushrooms and supports the revival of outdoor fungal bed cultivation in contaminated landscapes.

ecology↗

Dual inhibition of glutaminolysis and autophagy suppresses proliferation of Rheumatoid arthritis fibroblast-like synoviocytes and mitigates arthritis in SKG mice

Recent evidence highlights the critical role of immune metabolism in the pathogenesis of rheumatoid arthritis (RA). We previously demonstrated that glutaminase 1 (GLS1), a key enzyme in glutamine metabolism, is upregulated in fibroblast-like synoviocytes from RA patients (RA-FLS) and that GLS1 inhibition exerts an antiproliferative effect on RA-FLS. Glutaminolysis has also been shown to suppress autophagy, raising the possibilitiy that inhibiting glutaminolysis may enhance autophagy. Given this interplay, we hypothesized that dual inhibition of glutaminolysis and autophagy could synergistically suppress RA-FLS proliferation. This study aimed to investigate the effects of combining autophagy and glutaminolysis inhibition on RA-FLS and arthritis in SKG mice. We utilized chloroquine (CQ) as an autophagy inhibitor and compound 968 (C968), a GLS1 inhibitor, to suppress glutaminolysis. Treatment with C968 upregulated LC3B and ATG5 expression and increased LC3-II protein levels in RA-FLS, indicative of enhanced autophagy. Furthermore, C968 promoted autophagosome formation in RA-FLS. These findings confirm that glutaminolysis inhibition enhances autophagy in RA-FLS. The combination of C968 and CQ significantly inhibited RA-FLS proliferation and increased apoptotic cell death. Moreover, C968-CQ co-treatment markedly alleviated arthritis severity in SKG mice. Our findings suggest that concurrent suppression of glutaminolysis and autophagy represents a promising therapeutic strategy for RA.

immunology↗

mmVelo: A deep generative model for estimating cell state-dependent dynamics across multiple modalities

Single-cell multiomics provides unique insight into the regulatory relationships across different biological layers such as the transcriptome and regulome. However, single-cell multiomics is limited by its ability to capture only static snapshots at the time of observation, restricting the reflection of dynamic state changes orchestrated across modalities. RNA velocity analysis of single cells allows for the prediction of temporal changes in the transcriptome; however, the inferred dynamics cannot be applied across all biological layers, specifically in the regulome. Therefore, to address this limitation, we developed multimodal velocity of single cells (mmVelo), a deep generative model designed to estimate cell state-dependent dynamics across multiple modalities. mmVelo estimates cell state dynamics based on spliced and unspliced mRNA expression, and uses multimodal representation learning to project these dynamics onto chromatin accessibility, inferring chromatin velocity at a single-peak resolution. We applied mmVelo to single-cell multiomics data from a developing mouse brain and validated the accuracy of the estimated chromatin accessibility dynamics. Furthermore, using the estimated dynamics, we identified the transcription factors that are crucial for chromatin accessibility regulation in mouse skin. Finally, using multiomics data as a bridge, we demonstrated that during human brain development, the dynamics of missing modalities can be inferred from single-modal data via cross-modal generation. Overall, mmVelo enhances our understanding of the dynamic interactions between modalities, offering insights into the regulatory relationships across molecular layers.

bioinformatics↗

scSurv: a deep generative model for single-cell survival analysis

Single-cell omics analysis has unveiled the heterogeneity of various cell types within tumors. However, no methodology currently reveals how this heterogeneity influences cancer patient survival at single-cell resolution. Here, we introduce scSurv, combining a Cox proportional hazards model with a deep generative model of single-cell transcriptome, to estimate individual cellular contributions to clinical outcomes. The accuracy of scSurv was validated using both simulated and real datasets. This method identifies cells associated with favorable or adverse prognoses and extracts genes correlated with their contribution levels. In melanoma, scSurv reproduces known prognostic macrophage classifications and facilitates hazard mapping through spatial transcriptomics in renal cell carcinoma. We also identified genes consistently associated with prognosis across multiple cancers and demonstrated the applicability of this method to infectious diseases. scSurv is a novel framework for quantifying the heterogeneity of individual cellular effects on clinical outcomes.

bioinformatics↗

Endoplasmic reticulum patterns insect cuticle nanostructure

Insect cuticles with nano-level structures exhibit functional surface properties such as structural color and superhydrophobicity. Despite the enormous influence the cuticle has had on biomimetic industrial applications, molecular and cellular mechanisms of cuticular extracellular matrix (ECM) assembly into nanoscale structures remain poorly understood in insects and other taxa. Ghiradella (1989) described how a crystallin-like lattice of endoplasmic reticulum (ER) prefigures the patterning of the porous cuticle of the butterfly wing scale with structural color1. Building on that insight, we show that the nanopore structure of the olfactory (olf) organs, which serve as molecular filters in Drosophila, is built through a novel process in which ER material is trafficked to the plasma membrane mediated by the autophagy pathway. The process is controlled by the insect-specific protein Gore-tex/Osiris23 (Gox)2, which is localized to the tubular ER of olf hair cells. Gox recruits Ref(2)P, the fly counterpart of mammalian p62/SQSTM13, to initiate ER scission. The excised ER fragments are processed by autophagy to gain access to the plasma membrane and trigger membrane invagination, which plays a role in remodeling the cuticular envelope layer to the nanopore formation. This repurposing of the ER phagy for machinery to support the fabrication of nanoscale ECM by the Gox protein sheds light on the nanopatterning of insect cuticles and their genetic control.

developmental biology↗

Mechanical control of the insect extracellular matrix nanostructure

Nanoscale modifications of apical extracellular matrix (ECM) have created a variety of functional surfaces with distinct physical properties, as exemplified by structural coloration and superhydrophobicity in animals and plants1. While the surface nanostructures of various organisms have inspired numerous biomimetic applications, the biological mechanisms underlying ECM patterning at the nanoscale remain largely unknown. Here, we investigated the morphogenesis of cuticular pores in Drosophila olfactory organs2,3. Hundreds of uniform-sized nanopores of [~]50 nm permit selective access of odorant molecules to olfactory neurons. We showed that matrices composed of the zona pellucida domain (ZPD) protein4-6 cover sensory organs in cell type-specific patterns and combinations. The ZPD proteins Dyl, Tyn, Mey, and Nyo form matrices with specific mixing and sorting properties, restricting cell growth and movement. The disruption of ZPD matrices leads to detachment of the envelope layer of the cuticle from the plasma membrane, and reduced numbers and irregularly sized nanopores. Our results suggest that compressive force from the ECM is essential for robust nanopore morphogenesis. This work reveals a previously unrecognized role for ZPD proteins as modular units that establish the mechanical environment required to modulate the nanoscale assembly of cuticle materials, opening a new biological context to these biomimetically important structures.

developmental biology↗

Unsupervised deep learning enables blur-free super-resolution in two-photon microscopy

We developed an unsupervised deep learning method to simultaneously perform deblurring, super-resolution, and segmentation of two-photon microscopy images. Two-photon microscopy is an excellent technique for non-invasively observing deep biological tissues, but blurring during deep imaging has been a challenge. Conventional deblurring methods have limited performance and are not suitable for deblurring two-photon microscopy images. Moreover, methods that simultaneously perform segmentation, which is usually required in downstream analysis, have not been developed. Therefore, in this method (TENET), we precisely modeled the blur of two-photon microscopy and simultaneously achieved deblurring, super-resolution, and segmentation through unsupervised deep learning. In simulation and experimental data, we achieved deblurring, resolution improvement, and segmentation accuracy surpassing conventional methods. Furthermore, we applied the method to live imaging of microglia, enabling quantitative 3D morphological analysis that was previously difficult. This method allows non-invasive visualization of detailed structures in deep biological tissues, and is expected to lead to a more high-definition understanding of biological phenomena. Future applications to time-series morphological analysis of microglia are anticipated.

bioinformatics↗

Inferring extrinsic factor-dependent single-cell transcriptome dynamics using a deep generative model

1RNA velocity estimation helps elucidate temporal changes in the single-cell transcriptome. However, current methodologies for inferring single-cell transcriptome dynamics ignore extrinsic factors, such as experimental conditions and neighboring cell. Here, we propose ExDyn--a deep generative model integrated with splicing kinetics for estimating cell state dynamics dependent on extrinsic factors. ExDyn enables the counterfactual inference of cell state dynamics under different conditions. Among the extrinsic factors, ExDyn can extract key features which have large effects on cell state dynamics. ExDyn correctly estimated the difference in dynamics between two conditions and showed better accuracy over existing RNA velocity methods. ExDyn were utilized for unveiling the effect of PERK-knockout on neurosphere differentiation, hematopoietic stem cell differentiation driven by chromatin activity and the dynamics of squamous cell carcinoma cells dependent on colocalized neighboring cells. These results demonstrated that ExDyn is useful for analyzing key features in the dynamic generation of heterogeneous cell populations.

bioinformatics↗

Osiris gene family defines the cuticle nano-patterns of Drosophila

Nanostructures of pores and protrusions in the insect cuticle modify molecular permeability and surface wetting and help insects sense a variety of environmental cues. The cellular mechanism specifying cuticle nanostructures is poorly understood. Here, we show that insect-specific Osiris family genes are expressed in various cuticle-secreting cells in the Drosophila head in the early stage of cuticle secretion and collectively cover nearly the entire surface of the head epidermis. We show that each sense organ cell with various cuticular nanostructures expresses a unique combination of Osiris genes. Osiris gene mutations caused various cuticle defects in the corneal nipples of the eye and pores of the chemosensory sensilla. Osiris genes provide an entry point for investigating cuticle nanopatterning in insects.

developmental biology↗

A deep generative model for estimating single-cell RNA splicing and degradation rates

AO_SCPLOWBSTRACTC_SCPLOWMessenger RNA splicing and degradation are critical for gene expression regulation, the abnormality of which leads to diseases. Previous methods for estimating kinetic rates have limitations, assuming uniform rates across cells. We introduce DeepKINET, a deep generative model that estimates splicing and degradation rates at single-cell resolution from scRNA-seq data. DeepKINET outperformed existing methods on simulated and metabolic labeling datasets. Applied to forebrain and breast cancer data, it identified RNA-binding proteins responsible for kinetic rate diversity. DeepKINET also analyzed the effects of splicing factor mutations on target genes in erythroid lineage cells. DeepKINET effectively reveals cellular heterogeneity in post-transcriptional regulation.

bioinformatics↗

NEDD4-binding protein 1 suppresses HBV replication by degrading pgRNA

Chronic infection with hepatitis B virus (HBV) places patients at increased risk for liver cirrhosis and hepatocellular carcinoma. Although nucleos(t)ide analogs are mainly used for the treatment of HBV, they require long-term administration and may lead to the emergence of drug resistant mutants. Therefore, to identify targets for the development of novel anti-HBV drugs, we screened for HBV-suppressive host factors using a plasmid expression library of RNA-binding proteins (RBPs). We screened 132 RBPs using an expression plasmid library by measuring HBV relaxed circular DNA (rcDNA) levels in hepatocellular carcinoma. Our screen identified NEDD4-binding protein 1 (N4BP1) as having an anti-HBV effect. In hepatocellular carcinoma cell lines transfected or infected with HBV, overexpression of N4BP1 decreased rcDNA levels while knockdown or knockout of the gene encoding N4BP1 rescued rcDNA levels. N4BP1 possesses the KH-like and RNase domains and both were required for the anti-HBV effect of N4BP1. Additionally, we measured levels of HBV pregenomic RNA (pgRNA) and covalently closed circular DNA (cccDNA) in the RBP-transfected cells and confirmed that N4BP1 binds pgRNA directly and degraded both the 3.5 kb and 2.4/2.1 kb HBV RNA. In summary, N4BP1 is a newly identified host factor able to counteract HBV production by promoting the degradation of 3.5 kb and 2.1/2.4 kb HBV RNA. ImportanceThere is still a large number of HBV-infected people in the world today because of no curative treatment for HBV infection. In this study, we focused on and screened RNA-binding proteins to identify new host factors which inhibit HBV replication. As a result, we found that NEDD4-binding protein 1 (N4BP1) expression suppresses rcDNA production by promoting the degradation of pregenomic RNA, 2.4kb and 2.1kb HBV RNA. Furthermore, KH-like domain or RNase domain of N4BP1 were involved in this anti-HBV effect. In addition, the N4BP1 levels were lower in HCC resection samples of exacerbated patients, suggesting that individual N4BP1 levels might be related to HCC progression. This novel factor can potentially become a key to new HBV treatments.

microbiology↗

Surface-engineered extracellular vesicles to modulate antigen-specific T cell expansion for cancer immunotherapy

Extracellular vesicles (EVs), including exosomes, are emerging as novel mediators of cell-cell communications, involved in various processes such as immune activation and immunosuppression. Despite the recent development of several EVs-based cancer immunotherapies, their clinical efficacy remained limited. Here, using fusion with tetraspanin as one of the EV engineering techniques, we created antigen-presenting extracellular vesicles (AP-EVs) to reproduce the functional characteristics of professional antigen-presenting cells (APCs). AP-EVs were also equipped with surface-bound IL-2, a feature not inherent to APCs, which facilitated selective delivery of IL-2 to antigen-specific CD8+ T cells. AP-EVs were engineered to express a peptide-major histocompatibility class I (pMHCI) complex, a costimulatory CD80 molecule, and IL-2, allowing the simultaneous presentation of multiple immune modulators to antigen-specific CD8+ T cells. This promoted the clonal expansion and differentiation of antigen-specific cytotoxic T lymphocytes, leading to potent anticancer immune responses. Combination therapy with AP-EVs and anti-PD-1 demonstrated enhanced anticancer immunity against established tumors compared with anti-PD-1 monotherapy. Our engineered EVs represent a novel effective strategy for cancer immunotherapy.

bioengineering↗

Simple ways to avoid collecting highly 137Cs-contaminated Aralia elata buds

Collection and cooking of wild vegetables have provided seasonal enjoyments for Japanese local people as provisioning and cultural ecosystem services. However, the Fukushima Daiichi Nuclear Power Plant accident in March 2011 caused extensive radiocesium contamination of wild vegetables. Restrictions on commercial shipments of wild vegetables have been in place for the last 10 years. Some species, including buds of Aralia elata, are currently showing radiocesium concentrations both above and below the Japanese reference level for food (100 Bq/kg), suggesting that there are factors decreasing and increasing the 137Cs concentration. Here, we evaluated easy-to-measure environmental variables (dose rate at the soil surface, organic soil layer thickness, slope steepness, and presence/absence of decontamination practices) and the 137Cs concentrations of 40 A. elata buds at 38 locations in Fukushima Prefecture to provide helpful information on avoiding collecting highly contaminated buds. The 137Cs concentrations in A. elata buds increased significantly with increases in the dose rate at the soil surface. Meanwhile, the 137Cs concentration in A. elata buds were not reduced by decontamination practices. These findings suggest that measuring the latest dose rate at the soil surface at the base of A. elata plants is a helpful way to avoid collecting buds with higher 137Cs concentrations and aid in the management of species in polluted regions.

ecology↗

Multiscale modeling of HBV infection integrating intra- and intercellular viral propagation for analyzing extracellular viral markers

Chronic infection of hepatitis B virus (HBV) is caused by the persistence of closed circular DNA (cccDNA) in the nucleus of infected hepatocytes. Despite available therapeutic anti-HBV agents, eliminating the cccDNA remains challenging. The quantifying and understanding dynamics of cccDNA are essential for developing effective treatment strategies and new drugs. However, it requires a liver biopsy to measure the intrahepatic cccDNA, which is basically not accepted because of the ethical aspect. We here aimed to develop a non-invasive method for quantifying cccDNA in the liver using surrogate markers present in peripheral blood. We constructed a multiscale mathematical model that explicitly incorporates both intracellular and intercellular HBV infection processes. The model, based on age-structured partial differential equations (PDEs), integrates experimental data from in vitro and in vivo investigations. By applying this model, we successfully predicted the amount and dynamics of intrahepatic cccDNA using specific viral markers in serum samples, including HBV DNA, HBsAg, HBeAg, and HBcrAg. Our study represents a significant step towards advancing the understanding of chronic HBV infection. The non-invasive quantification of cccDNA using our proposed methodology holds promise for improving clinical analyses and treatment strategies. By comprehensively describing the interactions of all components involved in HBV infection, our multiscale mathematical model provides a valuable framework for further research and the development of targeted interventions.

microbiology↗