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Sengenes, C.

Publications and source records attributed to Sengenes, C..

3 recordsLinked to original sources

NUCGEN3D: A synthetic framework for large-scale 3D nuclear segmentation with open-source training data and models

AO_SCPLOWBSTRACTC_SCPLOWRobust nuclear segmentation in 3D microscopy images is a critical yet unresolved challenge in quantitative cell biology, hindered by the scarcity and variability of annotated volumetric datasets. Because such data are difficult to obtain, most state-of-the-art approaches, including Cellpose, segment individual 2D slices and then heuristically reconstruct 3D volumes, thereby losing critical spatial context. Our analysis of expert annotator performance confirms that ignoring 3D context introduces substantial variability in nuclear detection and annotation. While a few 3D models have been trained on small or toy datasets, no large-scale, openly available resource currently exists to enable robust training of high-capacity 3D segmentation networks. To address this, we present NucGen3D, a customizable simulation framework that generates large-scale, annotated 3D microscopy datasets from limited 2D input, specifically the 2018 Data Science Bowl dataset. NucGen3D produces realistic 3D volumes across diverse biological and imaging scenarios, including variations in nuclear morphology, spatial arrangement, acquisition artifacts, and imaging noise. Using this synthetic data, we trained two models from scratch: a 2D convolutional neural network under Cellpose-like conditions, and a fully 3D convolutional model that extends the 2D settings. We evaluated both on a challenging, independent real-world dataset with complex nuclear architectures. Both models, especially the 3D model, consistently outperformed state-of-the-art methods, including those trained on larger annotated datasets or based on more complex architectures. These results demonstrate that synthetic data can effectively substitute for real 3D annotations in training performing models at scale. To promote reproducibility and further research, we release both the NucGen3D framework and the fully trained 3D segmentation model as open source, making this the first end-to-end open resource for large-scale 3D nuclear segmentation.

bioinformatics↗

Mobilizable adipose stromal cells fuel regenerative adipogenesis in injured muscle

Skeletal muscle regeneration is a highly orchestrated process involving the dynamic interplay of multiple cell types. Among these, fibro-adipogenic progenitors (FAPs), a population of resident mesenchymal stromal cells (MSCs), are essential for creating a supportive microenvironment that promotes satellite cell differentiation and modulates immune responses. Our recent work revealed that adipose stromal cells (ASCs) from subcutaneous adipose tissue (ScAT) infiltrate the injured muscle within the first 24h post-injury, contributing significantly to the regenerative process. Consequently, the FAP population in the regenerating muscle comprises both resident FAPs and infiltrated ASCs. In the present study, using single cell RNA-seq in a mouse model with trackable KikGR+ ASCs and bioinformatics analyses, we identify Limch1+/Prg4+ ASCs as the primary Mobilizable ASCs (Mob-ASCs) that migrate to and infiltrate the injury site. Notably, this migration is detectable as early as 14 hours post-injury. We demonstrate that these cells are pre-activated within the ScAT, primed to initiate both migratory and regenerative programs. Intriguingly, bioinformatic inference of key activated transcription factors suggested that adipogenesis is also activated in these cells. Leveraging supervised machine learning, we tracked the fate of Mob-ASCs within the regenerating muscle post-injury, where they continue to execute these programs. Importantly, these cells lineage is cued towards a fate of adipogenesis. In vivo, we observed transient generation of adipocytes with a peak at 7-9 days post-injury to which infiltrated ASCs contributed. In vitro, conditioned media assays further revealed that adipocytes derived from ASCs--but not those from FAPs--enhance myoblasts fusion. Collectively, our findings establish Limch1+/Prg4+ ASCs as the Mobilizable ASC population and suggest that their transient adipogenic differentiation is beneficial for muscle regeneration.

physiology↗

The Mediator complex subunit Med19 extends healthy lifespan in Drosophila by preventing cellular and organismal frailty

Aging involves a progressive decline in physiological functions, often marked by the onset of a "frailty point" just before survival rates decrease rapidly. Here, we investigate how the Mediator subunit Med19 modulates this transition in Drosophila. We find that upregulating Med19 extends the median lifespan by nearly 90% and postpones the onset of accelerated mortality, suggesting that Med19 helps preserve the resilience phase of aging. In contrast, Med19 downregulation sharply reduces both median and maximum lifespan, advancing the frailty threshold. We show that Med19 knockdown increases fly vulnerability to environmental insults such as oxidative and genotoxic challenges whereas Med19 upregulation helps them resist these stresses, underscoring Med19s protective role in maintaining genomic integrity. We link these phenotypes to altered stress-response pathways at the cellular level: Med19-depleted cells show a compensatory upregulation of genes involved in iron-sulfur cluster biogenesis, glutathione metabolism, and DNA damage repair. At the cellular level, Med19 depletion triggers a "loser" phenotype in cell competition assays, activating the JNK pathway and undergoing apoptosis, highlighting a form of "cellular frailty" that parallels organismal frailty. Finally, we found that the Med19 protein level naturally decreases with age and showed that restoring Med19 expression in aged flies increases fitness and delays the onset of frailty even in older, "frail" individuals, underscoring its significance as an aging regulator. Altogether, our findings establish Med19 as a crucial mediator of lifespan and stress resilience, suggesting it acts as a rheostat that modulates the transition from healthy aging to frailty in Drosophila. GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=180 HEIGHT=200 SRC="FIGDIR/small/659864v1_ufig1.gif" ALT="Figure 1"> View larger version (54K): org.highwire.dtl.DTLVardef@1a5e398org.highwire.dtl.DTLVardef@14658org.highwire.dtl.DTLVardef@1b14089org.highwire.dtl.DTLVardef@41060_HPS_FORMAT_FIGEXP M_FIG C_FIG Highlights- At the organismal level, Med19 upregulation extends Drosophila lifespan by 90%, delays the onset of frailty and enhances oxidative and DNA damage stress resistance, while its depletion has the opposite effect. - Med19 depletion alters the expression of stress response genes and induces a loser-cell phenotype in cell competition assays revealing its crucial function in controlling cellular fitness. - Med19 protein levels naturally decline with age, and its restoration in aged flies improves both healthspan and lifespan.

cell biology↗