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Auduge, N.

Publications and source records attributed to Auduge, N..

4 recordsLinked to original sources

Epithelial density controls cell migration through an adhesion-nucleus mechanotransduction pathway

Cell density is thought to regulate tissue growth, homeostasis, and regeneration, yet how cells sense and respond to density remains poorly understood. To investigate density-dependent mechanotransduction, we combined genetically encoded biosensors with quantitative fluorescence microscopy in epithelial cells subjected to genetic, pharmacological, and mechanical perturbations. We found that low epithelial density promotes focal adhesion growth, causing mechanical relaxation of vinculin and release of its competitive binding with FAK and ERK. This enables FAK to bind and activate ERK in the cytoplasm. Cytoskeletal tension transmitted through LINC complexes drives their nuclear translocation, where low density induces ERK-dependent chromatin decondensation and increased nuclear envelope tension. This recruits and activates cPLA2, leading to arachidonic acid production and enhanced cell migration. Together, these findings identify a mechanochemical pathway linking cell density to epithelial migration via ERK, cPLA2, and mechanically regulated signaling from adhesions to the nucleus. Significance statementIn multicellular organisms, cells constantly experience crowding, yet how they detect changes in cell density and convert them into biological responses is not well understood. Here, we show how low cell density mechanically triggers signaling inside epithelial cells to promote migration. When cells are sparse, adhesion sites grow and release key signaling proteins that move into the nucleus stretched by the cytoskeleton. These mechanical and biochemical inputs alter nuclear structure, activates lipid signaling, and boosts cell migration. By revealing how mechanical forces, cell adhesions, and nuclear signaling work together, this study provides a clear mechanistic link between cell density and migration, a process central to tissue growth, repair, and disease progression.

cell biology↗

Chromosome condensation mechanically primes the nucleus for mitosis

Accurate transition into mitosis driven by cyclin B1-CDK1 activity is essential to avoid chromosome segregation errors and preserve genome integrity. How this activity is spatially controlled to trigger mitotic onset remains unclear. Here, we show that chromosome condensation triggers an increase in nuclear envelope (NE) tension. This increased tension is required for nuclear translocation of cyclin B1 and dynein loading on nuclear pore complexes (NPCs), ensuring timely mitotic entry. Micromanipulation experiments further indicate this tension-dependent mechanism requires SUN proteins on the NE. Disruption of chromosome condensation leads to an accumulation of the G2 checkpoint kinase Wee1 and inhibition of CDK1 activity, which result in a temporary delay in mitotic entry. This delay can be overridden by increasing tension on the NE, which accelerates the nuclear translocation of cyclin B1 and dynein loading. We propose that mitotic onset is controlled by a chromosome-dependent NE tension mechanism that enables robust spatiotemporal coupling between chromosome condensation and the structural changes required for an efficient mitosis.

cell biology↗

Collective directional memory controls the range of epithelial cell migration

Cell migration is a fundamental behavior in multicellular development, regeneration, and homeostasis, which is deregulated in cancer. Epithelial cells migrate individually when isolated and collectively within a tissue. However, how interactions between cells affect their ability to explore space and their sensitivity to guidance signals is poorly understood. We show that isolated cells that are persistent random walkers adopt a super-diffusive behavior in an epithelium. The effect is stronger than external guidance cues and enables cells to reach greater distances than when isolated. This behavior is consistent with a fractional Brownian motion that emerges from velocity coordination between neighboring cells with intact intercellular adhesion. Furthermore, we show how the molecular stability and mechanosensitivity of adhesion complexes, both linked to the ability of the adhesion protein vinculin to dimerize, ultimately regulate the speed of collective migration and the sensitivity to guidance signals. Together, our results show how cell speed, persistence, and directionality define the efficiency of spatial cell exploration on short, intermediate, and long time scales, respectively.

biophysics↗

Chromatin Condensation Fluctuations Rather Than Steady-State Predict Chromatin Accessibility

Chromatin accessibility to protein factors is critical for genome activities. Dynamic changes in nucleosomal DNA compaction and higher order chromatin structures are expected to allow specific sites to be accessible to regulatory factors and the transcriptional machinery. However, the dynamic properties of chromatin that regulate its accessibility are poorly understood. Here, we took advantage of the microenvironment sensitivity of the fluorescence lifetime of EGFP-H4 histone incorporated in chromatin to map in the nucleus of live cells the dynamics of chromatin condensation and its direct interaction with a tail acetylation recognition domain (the double bromodomain module of human TAFII250, dBD). We reveal chromatin condensation fluctuations supported by mechanisms fundamentally distinct from that of condensation. Fluctuations are spontaneous, yet their amplitudes are affected by their sub-nuclear localization and by distinct and competing mechanisms dependent on histone acetylation, ATP, and both. Moreover, we show that accessibility of acetylated histone H4 to dBD is not restricted by chromatin condensation nor predicted by acetylation, rather, it is predicted by chromatin condensation fluctuations.\n\nSignificanceIn higher eukaryotes, the structure and compaction of chromatin are considered as barriers to genome activities. Epigenetic marks such as post-translational modifications of histones can modify the structure and compaction of chromatin. The accessibility of protein factors to these epigenetic marks is therefore of paramount importance for genome activities. We reveal chromatin condensation fluctuations supported by mechanisms fundamentally distinct from that of condensation itself. We show that accessibility of acetylated histone H4 to double bromodomains is not restricted by chromatin condensation nor predicted by acetylation, rather, it is predicted by chromatin condensation fluctuations.\n\nClassificationBiological Sciences, Cell Biology

cell biology↗