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Dubreil, L.

Publications and source records attributed to Dubreil, L..

4 recordsLinked to original sources

Super-resolution imaging with deep learning-based segmentation for detailed characterization of mitochondrial arrangement in Pompe disease skeletal muscle

Pompe disease (glycogen storage disease type II) is an autosomal recessive lysosomal storage disorder caused by acid -glucosidase deficiency, leading to lysosomal glycogen accumulation, autophagosome buildup, and defective autophagic flux. Mitochondrial abnormalities, traditionally described by electron microscopy as paracrystalline inclusions, cristae loss, and swollen structures, have long been considered secondary consequences of lysosomal dysfunction. However, the spatial organization, organelle crosstalk, and fiber-type-specific progression of these alterations in skeletal muscle remain poorly understood. We combined super-resolution image scanning microscopy with deep learning-based segmentation to quantitatively assess mitochondrial and lysosomal remodeling, and their direct physical interactions, in Pompe disease (Gaa-/-) mice. Organelles were analyzed at pre-symptomatic (1 month) and symptomatic (4 months) stages across different muscle types (Soleus, Gastrocnemius), fiber types, and subcellular regions (subsarcolemmal, intermyofibrillar). Mitochondrial network structure was altered as early as 1 month of age, whereas density changes became widespread at 4 months in a fiber-type- and region-dependent manner. Alongside early lysosomal enlargement and late-stage spatial clustering, we observed a progressive, region-specific increase in mitochondria-lysosome contacts, most pronounced in the intermyofibrillar region. This quantitative framework provides a powerful tool for monitoring pathophysiology and evaluating therapeutic interventions in Pompe disease.

pathology↗

Identification of miR-187 as a modulator of early oogenesis and female fecundity in medaka

MicroRNAs (miRNAs) are known regulators of ovarian function in vertebrates, yet their physiological roles in fish reproduction remain poorly understood. Here, we identified miR-187 as one of the most ovarian-enriched miRNAs in medaka (Oryzias latipes) and we uncovered its function in vivo using CRISPR/Cas9-mediated gene inactivation. miR-187-3p is expressed in oocytes and granulosa cells in the ovary, and in discrete brain areas. Its loss-of-function leads to a significant reduction in female fecundity. High-resolution 3D imaging of whole ovaries revealed that mir-187 mutants accumulate early stage I follicles and show reduced progression to later stages, indicating a defect in early follicle recruitment and growth. Transcriptomic profiling of mutant ovaries revealed extensive gene-expression remodeling, including downregulation of key regulators of steroidogenesis, Wnt/{beta}-catenin signaling, and TGF-{beta} pathways, and upregulation of genes associated with early follicle activation and immature somatic cell states. Using an expression-based target-prediction pipeline, we identified several putative miR-187-3p targets, including nr6a1a (gcnf) and dpagt1, two genes previously implicated in oocyte differentiation and female fertility in mammals. Together, our results demonstrate that miR-187 acts as a previously unrecognized regulator of early folliculogenesis and female reproductive capacity in medaka, expanding the repertoire of miRNAs with essential in vivo roles in teleost oogenesis and female fecundity. AUTHOR SUMMARYSuccessful fish reproduction depends on the continuous production of oocytes within the ovary. This process depends on the coordinated development of germ cells and the supporting somatic cells. Although microRNAs (miRNAs) are known to post-transcriptionally regulate gene expression, their physiological roles in the fish ovary and female reproduction remain poorly understood. In this study, we used the medaka to investigate the function of miR-187, a miRNA strongly enriched in the ovary. By generating a CRISPR/Cas9 knockout line, we showed that females lacking miR-187 produce fewer eggs and display defects in early follicle development. Using whole-ovary 3D imaging, we found that mutant females accumulate early follicles that fail to progress through normal growth stages. Transcriptomic analyses revealed broad gene-expression changes affecting pathways involved in follicle activation, somatic cell maturation, and ovarian signaling. Our results demonstrate that miR-187 is a previously unrecognized regulator of early folliculogenesis and female fecundity in medaka. This work expands the landscape of miRNA-mediated regulation in the ovary and highlights the importance of post-transcriptional mechanisms in controlling reproductive success in teleosts. Grant supportThe DYNAMO project (French National Research Agency, ANR-18-CE20-0004). The OVOPAUSE project (French National Research Agency, ANR-22-CE45-00017-02). The IMMO project (INRAE Metaprogramme DIGIT-BIO).

developmental biology↗

Three-step scalable production of extracellular vesicles from pancreatic beta cells in stirred tank bioreactors promotes cell maturation and release of ectosomes with preserved immunomodulatory properties

Small extracellular vesicles (sEV) released by healthy beta cells are promising candidates for diabetes therapy thanks to their aptitude to modulate inflammation, to induce or maintain pancreatic function and to prevent pathogenic mechanisms. To advance the clinical development of therapeutics, there is a crucial need for scalable production methods. Stirred tank bioreactors (STR) are widely used in the industry due to their ability to provide homogeneous gas and nutrient supply, online monitoring, and efficient scale up. Anchorage- dependent cells can be cultured in STR on microcarriers or as spheroids, but may experience shear stress, which can affect sEV phenotype and function. Using pancreatic beta cells, this study identifies critical cell culturing parameters, including culture mode (monolayer vs. spheroids), medium formulation (with or without serum, glucose control), and process parameters (stirring, duration, cell density). The findings show that small spheroid culture promotes beta cell maturation without decreasing the yield of sEV per cell, despite a reduced cell surface exchange area. However, stirring increased expression of cellular stress markers and decreased cell viability. Set up of a three-step bioprocess allowed to maximize cell viability and sEV yields at high cell density over short production duration. sEV produced under these conditions maintained high purity, membrane integrity, and the aptitude to reduce T- lymphocyte proliferation and IFN-{gamma} cytokine secretion in a mixed lymphocyte reaction. Flow cytometry analysis revealed lower CD63/CD81 ratios in STR, indicating enhanced ectosome production. Switch from high glucose expansion to low glucose production medium further allowed to direct sorting of the antigen insulin into beta-sEV. This study demonstrates the feasibility of producing functional sEV from mature beta cells cultured as small spheroids, suitable for upscale. Production of sEV in STR may be particularly beneficial for ectosome- enriched compound loading for therapeutic applications. Graphical abstractRational development of a scalable bioprocess to control extracellular vesicles production & function. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=90 SRC="FIGDIR/small/611247v1_ufig1.gif" ALT="Figure 1"> View larger version (35K): org.highwire.dtl.DTLVardef@6eaefeorg.highwire.dtl.DTLVardef@a2da3borg.highwire.dtl.DTLVardef@1a58f35org.highwire.dtl.DTLVardef@5cfd1d_HPS_FORMAT_FIGEXP M_FIG C_FIG HighlightsO_LISmall 3D-spheroid culture promotes cell maturation C_LIO_LIStirring induces cellular stress responses & promotes ectosome release from the cytoplasmic membrane C_LIO_LIDesign of experiment efficiently enhances cell viability and EV yield with preserved immune-modulatory properties C_LIO_LIGlucose-starvation during the production phase directs insulin-sorting into extracellular vesicles C_LI

bioengineering↗

Molecular and functional diversity of distinct subpopulations of extracellular vesicles from stressed pancreatic beta cells: implications for autoimmunity

Beta cell failure and apoptosis following islet inflammation have been associated with autoimmune type 1 diabetes pathogenesis. As conveyors of biological active material, extracellular vesicles (EV) act as mediators in communication with immune effectors fostering the idea that EV from inflamed beta cells may contribute to autoimmunity. Evidence accumulates that beta exosomes promote diabetogenic responses, but relative contributions of larger vesicles as well as variations in the composition of the beta cells vesiculome due to environmental changes have not been explored yet. Here, we made side-by-side comparisons of the phenotype and function of apoptotic bodies (AB), microvesicles (MV) and small EV (sEV) isolated from an equal amount of MIN6 beta cells exposed to inflammatory, hypoxic or genotoxic stressors. Under normal conditions, large vesicles represent 93% of the volume, but only 2% of the number of the vesicles. Our data reveal a consistently higher release of AB and sEV and to a lesser extent of MV, exclusively under inflammatory conditions commensurate with a 4-fold increase in the total volume of the vesiculome and enhanced export of immune-stimulatory material including the autoantigen insulin, microRNA, and cytokines. Whilst inflammation does not change the concentration of insulin inside the EV, specific Toll-like receptor-binding microRNA sequences preferentially partition into sEV. Exposure to inflammatory stress engenders drastic increases in the expression of monocyte chemoattractant protein 1 in all EV and of interleukin-27 solely in AB suggesting selective sorting towards EV subspecies. Functional in vitro assays in mouse dendritic cells and macrophages reveal further differences in the aptitude of EV to modulate expression of cytokines and maturation markers. These findings highlight the different quantitative and qualitative imprints of environmental changes in subpopulations of beta EV that may contribute to the spread of inflammation and sustained immune cell recruitment at the inception of the (auto-) immune response. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=194 SRC="FIGDIR/small/003145v1_ufig1.gif" ALT="Figure 1"> View larger version (62K): org.highwire.dtl.DTLVardef@1bf7c79org.highwire.dtl.DTLVardef@85098dorg.highwire.dtl.DTLVardef@362e33org.highwire.dtl.DTLVardef@11349ab_HPS_FORMAT_FIGEXP M_FIG C_FIG Inflammation stimulates release of a heterogeneous population of beta EV with differential expression of immunogenic substances involved in immune cell recruitment and activation. HighlightsO_LIStress engenders an up to four-fold increase in the volume of the vesiculome and enhanced auto-antigen release C_LIO_LICytokines are selectively sorted into EV subspecies C_LIO_LITLR-binding microRNAs are enriched in sEV C_LIO_LIEV from stressed beta cells promote dendritic and macrophage cell activation C_LI

immunology↗