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Biology subjects

Meng, Y.

Publications and source records attributed to Meng, Y..

At least 19 recordsLinked to original sources

Stain Normalisation Does Not Consistently Improve Matched-Location Retrieval with Pathology Foundation Models

Pathology foundation models provide reusable representations for computational pathology, but staining- and scanner-induced variation may compromise the robustness and reproducibility of embedding-based analyses across acquisition settings. Stain normalisation is widely used to mitigate such colour variation, yet whether it improves retrieval with modern self-supervised pathology encoders remains unclear. We test whether stain normalisation improves cross-scanner and cross-staining image retrieval using the PLISM whole-slide image subset, comprising 13 co-registered images of serial sections prepared under different staining conditions and digitised using seven scanners (91 whole-slide images). We sample 400 matched locations across the 91 images, yielding 36,400 tile instances. We compare two DINOv2-based encoders, Phikon-v2 (1,024-dimensional) and Midnight-12k (3,072-dimensional), with Reinhard and Macenko normalisation against an unnormalised baseline. Performance is measured using paired top-1 nearest-neighbour retrieval accuracy in two settings: cross-scanner retrieval of the same physical section digitised by different scanners, and cross-staining retrieval across co-registered images of serial sections, which differ in staining condition and may also contain section-level morphological variation. Neither normalisation method consistently improves top-1 retrieval relative to no normalisation, while Macenko reduces accuracy by up to 18.3 percentage points. An exploratory UMAP of unnormalised Midnight-12k slide-level mean embeddings showed partial overlap between scanner groups in a two-dimensional projection. These results challenge the routine use of stain normalisation in foundation-model retrieval pipelines and support validating preprocessing choices for each encoder and retrieval setting.

pathology↗

Consensus Formation History Shapes Collective Updating

Consensus is rarely a one-off achievement. In a changing world, groups must repeatedly update judgments they have already agreed upon, making consensus updating a common feature of real-world collective decisions. However, previous research on collective decision-making has focused mainly on how groups reach a single consensus, leaving the updating of established consensus largely unexamined. This raises two unanswered questions: does consensus updating involve biases analogous to sunk cost, and are such biases related to the cost of the previous consensus? Building a Fake Consensus paradigm, we manipulated consensus-formation cost and examined how dyads updated a subjectively established consensus after new information arrived. An independent individual experiment provided information-matched updating baselines, allowing us to determine whether dyads updated less or more than individuals responding to the same evidence. Contrary to sunk-cost predictions, low-cost consensus led dyads to update less than the individual baseline, whereas medium- and high-cost consensus led them to update more. The pathway through perceived consensus sharedness was significant, and the association between sharedness and updating was stronger at higher left temporoparietal junction inter-brain synchrony. These findings indicate that the history of consensus formation shapes subsequent updating by altering the psychological meaning of shared endorsement, while interpersonal alignment determines how this shared experience translates into coordinated behavior. To our knowledge, this is the first experimentally controlled study of consensus updating in teams to isolate formation history from actual disagreement, providing a new paradigm for studying how collective judgments change after agreement.

neuroscience↗

Characterization of tri-culture alveolar-like organoids to study fibrotic lung diseases

Rationale: Fibrotic interstitial lung diseases are progressive disorders characterized by lung scarring and declining respiratory function. Repeated injury and dysregulated epithelial-mesenchymal crosstalk are implicated in disease pathogenesis but remain incompletely understood. Three-dimensional (3D) organoids incorporating epithelial-mesenchymal crosstalk provide a physiologically relevant platform for investigating these mechanisms. Here, we present a 3D tri-co-culture alveolar organoid model and evaluate its responses to two profibrotic stimuli, TGF-{beta} and bleomycin. Methods: CI-huArlo, NCI-H441, and MRC-5 cells were co-cultured for 14 days to generate alveolar-like organoids. Cell marker expression was assessed by immunofluorescence (IF). To test injury response, organoids were exposed to TGF-{beta} (50 ng/mL) or bleomycin (20 g/mL) for 48 hours and characterized. Supernatants were collected to assess interleukin 8 (IL-8) and procollagen I by ELISA. qPCR assessed expression of CDKN1A and COL1A1 following treatments. Bulk RNA sequencing (RNA-seq) evaluated the transcriptomic responses to fibrotic stimulus. Results: Cellular marker expression was confirmed using IF for aquaporin-5 (alveolar type I cell marker) and TE-7 (fibroblast marker). Bleomycin exposure reduced viability and significantly increased IL-8 (126.3 {+/-} 16.86 vs. 48.88 {+/-} 4.470 pg/mL; p = 0.0002; N=6), with no change in secreted procollagen I compared to control. TGF-{beta} stimulation significantly increased secreted procollagen I (149.6 {+/-} 27.07 vs. 53.38 {+/-} 5.672 pg/mL; p <0.0001; N=6) without affecting viability or IL-8 release. qPCR resulted in no change in CDKN1A expression, while COL1A1 expression was increased with TGF-{beta} treatment compared with control and bleomycin. RNA sequencing demonstrated distinct and reproducible transcriptional responses to TGF-{beta} and bleomycin. TGF-{beta} induced 750 significantly upregulated and 641 downregulated genes, including increased COL1A1, COL4A1, FN1, and TGFB1, with enrichment of epithelial-mesenchymal transition and TGF-{beta} signalling programs. In contrast, bleomycin induced 953 significantly upregulated and 552 downregulated genes relative to untreated controls and was characterized by p53 signalling, DNA-damage responses, and reduced cell-cycle progression. Reference-state analysis further indicated reduced normal alveolar epithelial signatures following both treatments, with TGF-{beta} producing the strongest aberrant basaloid and myofibroblast-associated signatures. Conclusions: Tri-culture alveolar-like organoids exhibited stimulus-specific responses in a 3D multicellular system, supporting their use for mechanistic studies of epithelial-mesenchymal crosstalk, environmental exposures, and therapeutic responses.

cell biology↗

Reelin coordinates neuronal positioning and Müller glia scaffold maturation during retinal development

Reelin is a secreted extracellular matrix protein that regulates neuronal migration and layer formation in the developing brain, yet its role in retinal development remains incompletely defined. Here, we investigated Reelin function in retinal lamination using wild-type and Reeler (Reln-/-) mice, combining stage-resolved RNA in situ hybridization, immunohistochemistry, and single-nucleus RNA sequencing. We show that Reln is dynamically expressed in ganglion cell layer and inner nuclear layer neurons during retinal development and persists in discrete adult neuronal populations. Loss of Reelin leads to widespread defects in retinal organization affecting both neurons and Muller glia. In Reln-/- retinas, Muller glia exhibit reduced Glul positive extensions, indicating impaired glial scaffold maturation. Early-born neuronal populations are also disrupted, with altered spatial organization markers associated with retinal ganglion cell differentiation within the ganglion cell layer at postnatal day 9. Horizontal cells are significantly reduced with dorsal-predominant vulnerability, while cone photoreceptors are generated in normal numbers but show incomplete positioning within the outer nuclear layer. Together, these findings identify Reelin as a key regulator of retinal lamination that coordinates neuronal positioning with Muller glia morphogenesis, extending its canonical role in brain development to the vertebrate retina.

developmental biology↗

A multimodal foundation model linking histopathology and DNA methylation

Hematoxylin and eosin (H&E) slides are routinely available in cancer care, but molecular profiling often requires additional tissue processing and turnaround time. We introduce HistoMethyl, a DNA methylation-aware pathology foundation model that aligns whole-slide histopathology with matched genome-scale methylation beta-value profiles during pre-training while requiring only an H&E slide at inference. We evaluated HistoMethyl across four task groups: gene mutation prediction, morphology-associated classification, overall survival prediction, and direct DNA methylation beta-value recovery. Evaluation spanned TCGA cross-validation, a disease-held-out lower-grade glioma cohort, and external cohort validation in CPTAC glioblastoma and SurGen rectal adenocarcinoma, totaling 14 cancer cohorts and 81 gene mutation tasks. The best-performing configuration improved mean mutation AUROC by 5.03 percentage points. By converting DNA methylation supervision into an H&E-only representation, His-toMethyl could support an early molecular triage layer that helps prioritize cases for confirmatory sequencing, methylation profiling, immunohistochemistry, and molecular tumor board review. These image-only predictions are intended to accelerate downstream molecular testing and tissue allocation while leaving final diagnosis and treatment selection anchored in validated molecular assays.

Cancer Biology↗

Hearing Lips and Seeing Voices After Fifty Years: A Large-Scale McGurk Illusion Dataset for Audiovisual Speech Research

Efficient face-to-face communication relies on the integration of auditory speech and visual articulatory signals. Over the past five decades, the McGurk illusion has been widely used as an index of audiovisual speech integration. However, substantial variabilities in susceptibility to the illusion across participants and speakers limit its reliability as a stable measure of audiovisual integration ability. Here, we introduce the McGurk illusion dataset (MID), which, to our knowledge, is the largest publicly available McGurk stimulus dataset to date. The MID comprises auditory (N = 400), visual (N = 400), and audiovisual (N = 640) speech stimuli generated from 80 Mandarin speakers and validated through behavioral judgments across 360,900 trials. Using this dataset, we characterized the acoustic and facial articulatory properties of McGurk stimuli, replicated substantial inter-participant and inter-speaker variabilities in illusion susceptibility, and revealed the associations between variations in McGurk illusion rate and the variations in unisensory perception, audiovisual correspondences, and speakers characteristics. Furthermore, the stimulus set enabled systematic comparisons of the reliability of different McGurk illusion-based indices of audiovisual speech integration. Overall, the MID not only provides a standardized resource for investigating audiovisual speech integration and its alterations across populations, but also supports research on speaker normalization, lip-reading, and speech perception.

neuroscience↗

Integrating Histology with Spatial Molecular Programs Using a Multimodal Foundation Model

Histopathological assessment remains central to cancer diagnosis and stratification, yet its mechanistic interpretation remains limited without molecular context. To address this, we developed SQUALL, a multimodal foundation model integrating histology with spatial molecular programs. For pretraining, we assembled histMol, a large-scale corpus of 1.76 billion paired histology-spatial transcriptomics spots/bins across 33 tissues and 12 platforms from 3,446 tissue sections. Following pretraining, SQUALL enables transcriptome-wide virtual biomarker profiling, prognostically relevant spatial niches discovery, and integrative disease progression modeling. Leveraging its multimodal embeddings, SQUALL identifies niches associated with tertiary lymphoid structure (TLS) maturation and ovarian cancer relapse, reconstructs molecular trajectories of breast cancer invasion across 325,112 spots, and uncovers underlying transcriptional programs. Applied to whole-slide images from 898 patients, SQUALL outperforms existing pathology foundation models in outcome prediction while enabling interpretable risk stratification. Together, these results establish spatially aligned multimodal pretraining as a new paradigm for extending molecular insights into pathology images.

bioinformatics↗

MRI-based dental maturity in newborns reflects prenatal exposures and predicts timing of primary tooth eruption

Primary tooth development is shaped by prenatal experience and has consequences for childhood caries and lifelong oral health. However, evidence linking prenatal conditions to dental development has relied largely on postnatal proxies, such as parent-recalled eruption timing, that conflate prenatal programming with postnatal exposures. Here, we directly phenotype developing dentition in vivo using routinely acquired neonatal brain MRI. Using T2-weighted imaging from the HEALthy Brain and Child Development Study, we trained a 3D U-Net on 100 semi-automatic labels and applied the model to 1,433 quality-controlled neonatal scans. Automated post-processing extracted quantitative features of tooth volume, mineralization, and arch geometry. These features were used to predict postmenstrual age at MRI and to derive a bias-corrected tooth age gap (TAG), indexing relative dental maturity at birth. The segmentation model achieved mean cross-validated Dice = 0.94. Dental features predicted postmenstrual age with R2 = 0.30 and mean absolute error = 6.7 days, outperforming standard anthropometric measures (R2 = 0.22). In adjusted models, TAG varied by infant sex and was associated with gestational age at delivery, maternal pre-pregnancy BMI, and prenatal tobacco use. In infants with longitudinal dental follow-up, greater dental maturity at birth predicted earlier first tooth emergence and more teeth at one year. Automated segmentation and age prediction generalized to an independent cohort. These findings establish neonatal dental MRI phenotyping as an objective, scalable index of dental maturation and a potential readout of prenatal influences on a developmental system relevant to lifelong oral health. Significance StatementPrimary tooth development begins before birth and is shaped by intrauterine experience, with consequences for eruption timing, enamel quality, childhood caries, and lifelong oral health. Yet newborn dentition has been difficult to study because unerupted primary teeth are not routinely measurable at birth, forcing reliance on postnatal proxies that mix prenatal influences with later exposures. We show that standard newborn brain MRI can be repurposed to quantify dental maturity before postnatal exposures accumulate. Applied to 1,433 newborns, this open-source pipeline provides spatially localized measures of unerupted tooth development and links neonatal dental maturity to clinical, environmental, and eruption outcomes. These findings establish neonatal dental MRI as a scalable tool for studying how intrauterine experience becomes biologically embedded in dental development.

developmental biology↗

Targeting THOC2-Mediated mRNA Export Induces PARP Inhibitor Vulnerability in DNA Repair-Competent Hepatocellular Carcinoma

Hepatocellular carcinoma (HCC) remains a lethal malignancy with limited therapeutic options. While Poly (ADP-ribose) polymerase inhibitors (PARPi) exploit synthetic lethality in tumors with DNA repair defects, their clinical utility in HCC is hindered by the low prevalence of canonical repair gene mutations and the enhancing DNA repair capacity. Through proteomic analysis of two independent cohorts (n=260), we identified the THO complex component THOC2 as a master regulator of DNA damage response (DDR) via mRNA nuclear export control. Clinically, THOC2 overexpression predicted poor survival (HR=2.68-6.84, P<0.001) and correlated with enhanced DDR gene expression. Mechanistically, THOC2 chaperones mRNA nuclear export of DDR effectors (MDC1, PRKDC, MSH6) and proliferation drivers (TOP2A), thereby establishing a dual pro-repair/pro-growth program. Targeting this vulnerability, THOC2 knockdown induced synthetic lethality with PARPi, reducing Olaparib IC50 by up to 61% and suppressing tumor growth by 76% (P<0.001). Our study illuminates mRNA transport as a druggable DDR modulator and establishes THOC2 as both a prognostic biomarker and a therapeutic target to overcome PARPi resistance in HCC. This work pioneers a strategy to expand synthetic lethality beyond genetic defects by targeting post-transcriptional regulation.

cancer biology↗

FASN Inhibition Resensitizes Chordoma to Radiotherapy by Targeting Adaptive Unsaturated Fatty Acid Metabolism

SUMMARYChordoma, a rare malignant notochordal tumor of the skull base and spine, is typically resistant to chemotherapy and radiotherapy and exhibits aggressive local recurrence. Here we show that chordoma recurrence correlates with a coordinated upregulation of monounsaturated fatty acids (MUFAs) and polyunsaturated fatty acids (PUFAs), a low PFA/MUFA ratio and an adaptive, lipid peroxidation-resistant state that protects against DNA damage and cell death. Single-cell metabolic profiling identified a tumor subpopulation marked by a fatty acid biosynthesis-high state coupled to stemness. RT-tolerance was directly linked to elevated FASN and lipid droplet (LD) expansion, and MUFA-loading phenocopied RT-tolerance in chordoma cells. Mechanistically, LDs accumulated in response to RT via generation of ROS, and subsequent activation of ER-stress, SREBP1 and Fatty Acid Synthetase (FASN). DESI-MS showed that low-dose irradiation was sufficient to increase MUFAs early and build peroxidation resistant MUFA-LDs, whereas PUFA induction required a higher radiation dose. In a spatially defined manner in a patient-derived xenograft. Finally, in silico knockout and pharmacologic FASN blockade restored radiosensitivity and apoptosis in vitro and in vivo. Collectively, our result support a unifying model in which RT resistance in chordoma is shaped by an adaptive fatty acid metabolic program that buffers oxidative injury and increases survival of RT-resistant, stem-like tumor subpopulations. These findings further support FASN inhibition as a practical radiosensitization strategy for chordoma particulary where RT dose escalation is constrained by anatomy. KEYPOINTSO_LIRecurrent chordoma exhibits fatty acid-associated metabolic reprogramming. C_LIO_LIMUFA-associated lipid droplet accumulation is linked to radioresistance in chordoma cells. C_LIO_LITargeting FASN restores radiotherapy sensitivity of chordoma in vitro and in vivo. C_LI IMPORTANCE OF STUDYThis study underscores the clinical importance of targeting metabolic vulnerabilities to restore radiosensitivity in chordoma. By integrating transcriptomics, metabolomics, and in vitro and in vivo models, we identified adaptive fatty acid metabolic reprogramming as a central mechanism of RT resistance in chordoma. Recurrent tumors were characterized by coordinated enrichment of unsaturated fatty acids, especially monounsaturated fatty acids (MUFAs), together with a low PUFA/MUFA ratio and a lipid peroxidation-resistant state. Mechanistically, RT-tolerance chordoma cells exhibited a high-FASN state driven by activation of the ROS-ER stress-PERK/SREBP1/FASN axis, leading to intracellular lipid droplet expansion. Importantly, genetic and pharmacologic inhibition of FASN restored radiosensitivity and enhanced apoptosis in both in vitro and in vivo models, suggesting a translatable therapeutic strategy. Together, these findings link adaptive metabolic reprogramming to RT resistance and support new therapeutic approaches for chordoma management.

cancer biology↗

Liquid Phase Backscattered Scanning Electron Microscopy of Bacillus subtilis Spores

Backscattered electron scanning electron microscopy (BSE-SEM) provides compositional image contrast but has found limited application to biological samples due to the low atomic number difference between constituent elements, the thickness of the surrounding environment, and the need for complex sample preparation. Here, we demonstrate the use of room temperature liquid phase BSE-SEM (LPBSEM) for imaging Bacillus subtilis spores encapsulated in graphene liquid cells, preserving native hydration and reducing the thickness of the sample environment. This approach eliminates the need for staining and enables high-contrast visualisation of subcellular structures. Distinct structural layers within B. subtilis spores have been observed with a contrast similar to conventional thin-section transmission electron microscopy but without the need for sample preparation that potentially compromises sample integrity. We further investigate the influence of beam energy on the interaction volume depth and image contrast and propose optimal conditions for subsurface visualisation. Monte Carlo simulations have been used to validate our experimental observations and provide a quantitative framework for understanding BSE generation from hydrated, low atomic number specimens.

microbiology↗

The diversity of lesion network mapping findings

Lesion network mapping (LNM) has emerged as a popular framework to map the network mechanism of brain disorders using lesions and normative brain connectome (NBC)1. It was first demonstrated in neurological symptoms and was rapidly extended to a broad range of brain disorders in the past decade. A recent study by Van den Heuvel et al. questioned the methodological foundations of LNM2. We here raise concerns regarding their errors and biases in the methodology and visualization. The conclusion of that study--LNM maps circumscribed brain changes mostly to one and the same outcome--is not supported by the data presented.

neuroscience↗

Spatial proteomic mapping of the human and mouse retina using IBEX

PurposeTo generate a comparative spatial proteomic atlas of the human and mouse retina using a refined highly multiplexed immunohistochemistry technique called Iterative Bleaching Extends Multiplexity (IBEX). MethodsWe refined the IBEX workflow by integrating an antibody removal option alongside chemical bleaching. This dual strategy enabled removal of the entire antibody complex allowing for the flexible use of antibodies from the same host species across iterative cycles. Spatial proteomic data were cross-correlated to existing scRNAseq datasets. We also coupled this workflow with super-resolution imaging via deconvolution and applied it to the retina of healthy human, mouse and the Crb1rd8 mouse model. ResultsWe successfully imaged over 25 protein markers on human and mouse tissue sections, to generate spatial atlases of the major retinal cell populations. Cross-species protein expression was compared to scRNAseq datasets to identify protein and transcript disparities. Super-resolution IBEX delineated the ultrastructural features of the outer limiting membrane (OLM), identifying CD44 as a core structural component tightly co-localised with a highly organised F-actin belt within Muller glial endfeet. Using the Crb1rd8 mouse model, disruption of this complex was spatially associated with rosette formation and OLM structural failure. ConclusionSpatial proteomic atlases of the human and mouse retina were generated and correlated to transcriptional data, revealing insights into the arrangement of major retinal cell populations and OLM structure.

neuroscience↗

Mapping the latent CRBN-molecular glue degrader interactome

Molecular glue degraders (MGDs) are a transformative modality in drug discovery. MGDs that work in concert with the E3 ligase CRL4CRBN can degrade a range of substrates through tailored MGDs. To explore CRL4CRBN reprogrammability, we tested whether reported CRBN-MGD substrates are part of a network of latent CRBN interactors, detectable with generic CRBN-MGDs. Leveraging highly parallel interaction measurement (GluePCA) between CRL4CRBN and human zinc-fingers (ZFs), we identified [~]210 ZFs bound to CRBN-pomalidomide, where top binders are already reported as degraded by dedicated MGDs. To map latent CRBN-MGDs interactions proteome-wide, and thus define the immediately accessible CRBN target space, we combined AI-derived protein surface queries (MaSIF-mimicry) with GluePCA. This pipeline identified 6 known and 43 novel CRBN-pomalidomide binders, thereby providing privileged starting points for MGD development. We expect this binding-focused, highly parallel workflow to be readily applicable to other MGD/E3 ligase systems, extending the target landscape of this emerging drug class.

molecular biology↗

Integrative spatial multi-omics reveals prognostic tumor niches in female genital tumors

Female genital tumors (FGTs), including ovarian, endometrial, and cervical cancers, pose a major global health challenge, yet their spatial and molecular determinants of progression and therapy resistance remain poorly understood. Here we present a large-scale integrative spatial and multi-omics atlas of FGTs, combining exome, transcriptome, methylome, and miRNA sequencing with high-resolution Visium HD spatial transcriptomics, profiling over 62 million cells from 100 tumors. We show that HPV-driven suppression of TGF{beta} signaling in cervical cancer disrupts myofibroblast (myCAF) formation and reshapes immune infiltration, while serous tumors exhibit extensive oncogene amplifications that activate MYC and PI3K pathways, linking chromosomal instability (CIN) to proliferative, immune-cold phenotypes. In high-grade serous ovarian cancer, we identify a previously unrecognized malignant domain, the Proliferating Core Desert (PCD) niche, defined by CIN-high epithelial enrichment, immune exclusion, stromal protection, and chemotherapy resistance, maintained through crosstalk with macrophages and fibroblasts. Finally, we develop POWER, a pathology foundation model that predicts PCD niche abundance from routine H&E slides, enabling robust stratification of prognosis and anti-angiogenic therapy response.

genomics↗

The transcriptional regulatory circuit as a driver and therapeutic target in CML blast crisis

Patients with blast crisis in chronic myeloid leukemia (CML) exhibit an extremely poor prognosis, with median survival of only a few months and limited therapeutic options. Dysregulated transcriptional regulation plays a pivotal role in driving blast crisis progression. In this study, we performed histone modification and transcriptomic high-throughput sequencing on bone marrow cells derived from chronic and blast-phase CML patients, identifying a CML blast-specific transcriptional regulatory circuit comprising MEF2C, MYB, MEIS1, and ZEB2. These transcription factors (TFs) form protein complexes that co-bind to shared enhancers or promoters, reciprocally enhancing each others transcriptional activity and that of their downstream targets. Mechanistically, this circuit synergistically reprograms chromatin accessibility and transcriptional landscapes in blast cells, parallel activation of purine metabolism and Rho GTPase signaling pathways which exhibit functional crosstalk. Functional validation demonstrated that silencing components of this circuit or its downstream core targets significantly suppressed CML blast progression in vitro and in vivo. Notably, mebendazole (MBZ), a clinically approved inhibitor targeting MYB protein stability, recapitulated these inhibitory effects. Our findings establish the MEF2C-MYB-MEIS1-ZEB2 transcriptional circuit as a central driver of CML blast crisis and position MBZ as a high-potential translational strategy for targeting this lethal phase of the disease. Key PointsO_LIMEF2C, MYB, MEIS1, and ZEB2 form the CML blast-crisis transcriptional circuit, synergistically reprogramming chromatin and transcription. C_LIO_LIMebendazole inhibits CML blast progression by impairing the circuit, offering a rapid translational strategy for this lethal phase. C_LI

cancer biology↗

Identification and Domestication of a Wild Edible Oyster Mushroom Growing on Loblolly Pine (Pinus taeda) in Mississippi

The oyster mushroom is among the most extensively cultivated edible mushrooms worldwide. These mushrooms typically thrive on decaying broadleaf deciduous trees but are rarely found on conifers. A wild oyster mushroom strain was collected from pine trees in Mississippi. We characterized the strain using both morphological and molecular techniques. Pure cultures of this strain were obtained and utilized for spawn production, cultivation, genomic DNA extraction, and identification. Our research assessed the strains capacity to produce extracellular enzymes. The results demonstrated that the strain belonged to the species Pleurotus ostreatus (GenBank: PV750134).This fungal strain exhibited a significant ability to colonize lignocellulosic substrates derived from pine, such as logs and sawdust, as evidenced by the substantial production of laccase and cellulase enzymes. Pine logs yielded fruiting bodies approximately 60 days after inoculation. The mushroom strain, ASU_Pre_1-1, shows great potential for producing edible oyster mushrooms using pine wood waste in Mississippi.

ecology↗

β-catenin controls Afadin cortical recruitment to regulate planar epithelial cell division

Mitotic spindle orientation is tightly controlled in epithelia to preserve polarized tissue architecture. Here, we uncover a previously unrecognized role of the adherens junction protein {beta}-catenin in regulating planar mitotic spindle positioning required for symmetric epithelial cell division. Using CRISPR/Cas9-mediated genome editing in MDCK cells, we found that {beta}-catenin--but not its close homolog {gamma}-catenin (plakoglobin)--is required for proper spindle orientation. Loss of {beta}-catenin disrupts astral microtubule anchorage and impairs the localization of LGN-NuMA spindle orientation machinery. Mechanistically, {beta}-catenin mediates spindle regulation via its N-terminal domain, independently of {beta}-catenin binding. We showed that the cortical recruitment of Afadin during mitosis depends on {beta}-catenin, but surprisingly, overexpression of either Afadin or ZO-1 rescue the spindle orientation in {beta}-catenin deficient cells by restoring cortical LGN. Afadin depletion or dominant-negative Afadin abolished ZO-1-mediated compensation, thereby establishing Afadin as the central cortical integrator, potentiated by {beta}-catenin, and operating through mass-action to recruit cortical LGN. Together, our findings define {beta}-catenin as an upstream regulator of the Afadin-based cortical-spindle linkage that coordinate the crosstalk between adherens junctions and mitotic geometry to ensure epithelial homeostasis.

cell biology↗