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Jouy, C.

Publications and source records attributed to Jouy, C..

3 recordsLinked to original sources

Targeting skin ageing at the source: a novel cellular reprogramming approach using natural extract combinations

Cellular senescence is a driver of skin ageing that leads to structural deterioration and aesthetic changes. This study evaluated a novel senomorphic strategy, using synergistic combinations of natural small molecules to target RNA splicing regulation via upstream ERK/AKT signaling pathways. Nature-identical synthetic molecules, and corresponding extracts were assessed for cytotoxicity, impact on senescent cell load, proliferation, DNA damage load and SASP markers in naturally aged human primary skin cells. A topical, simple formulation was evaluated for impact on senescence and skin structure using 3D human ex vivo full-thickness skin explants exposed to 1.5 J/cm2 UVC irradiation. Combination of H. lupulus and G. biloba extracts produced a dose-dependent senomorphic impact of up to 45% in aged dermal fibroblasts and 10% in aged human primary keratinocytes (p [≤] 0.0001 & 0.001), without inducing cell proliferation. A 50% decrease in DNA damage load was also observed (p [≤] 0.0001). Qualitatively, the simple formulation mitigated UV-induced epidermal hyperplasia, restored collagen fiber organization, and reduced markers of senescence and inflammation. Targeting cellular senescence is an emerging traction point to address the root biological causes of skin ageing. Targeting the splicing dysregulation/senescence axis using combinations of natural plant extracts may provide a novel mode of action to reprogram senescent cells for repair and protection of skin structure and function.

cell biology↗

Development and application of SNP markers to facilitate DUS testing in tomato

Variety registration in Europe requires the evaluation of Distinction, Uniformity, and Stability (DUS) based on multi-environment trials and extensive phenotyping. The integration of molecular markers into DUS testing offers opportunities to increase efficiency and reduce costs, particularly in tomato (Solanum lycopersicum L.), a species characterized by rapid varietal turnover. We developed a high-density SNP genotyping resource targeting gene-rich regions across the tomato genome and applied it to a panel of 300 varieties registered over the past five decades. Temporal patterns of genetic diversity were assessed and compared with those observed in a collection of heirloom accessions predating 1970. Genome-wide association studies (GWAS) were conducted for 50 DUS traits to identify marker-trait associations and evaluate the potential of SNPs to complement phenotypic descriptors. Detected associations were compared with previously reported genes and quantitative trait loci (QTLs), enabling the validation of known loci and the identification of novel candidate genomic regions underlying trait variation. Finally, we assessed the discriminatory power of selected subsets of informative SNPs for variety distinction and grouping. Our results demonstrate the potential of integrating genomic and phenotypic data to enhance the robustness, resolution, and scalability of DUS testing in tomato.

Plant Biology↗

microRNA-dependent regulation of biomechanical genes establishes tissue stiffness homeostasis

The mechanical properties of tissues, which are determined primarily by their extracellular matrix (ECM), are largely stable over time despite continual turnover of ECM constituents 1,2. These observations imply active homeostasis, where cells sense and adjust rates of matrix synthesis, assembly and degradation to keep matrix and tissue properties within the optimal range. However, the regulatory pathways that mediate this process are essentially unknown3. Genome-wide analyses of endothelial cells revealed abundant microRNA-mediated regulation of cytoskeletal, adhesive and extracellular matrix (CAM) mRNAs. High-throughput assays showed co-transcriptional regulation of microRNA and CAM genes on stiff substrates, which buffers CAM expression. Disruption of global or individual microRNA-dependent suppression of CAM genes induced hyper-adhesive, hyper-contractile phenotypes in multiple systems in vitro, and increased tissue stiffness in the zebrafish fin-fold during homeostasis and regeneration in vivo. Thus, a network of microRNAs and CAM mRNAs mediate tissue mechanical homeostasis.

cell biology↗