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Biology subjects

Schelle, J.

Publications and source records attributed to Schelle, J..

2 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↗

Non-canonical cytokinesis driven by mechanical uncoupling via nematic flows and adhesion-based invagination

Cleavage - the series of rapid cell divisions that follow fertilization - marks the onset of metazoan development and represents a deeply conserved evolutionary process. Across animals, two principal modes exist: complete (holoblastic) and incomplete (meroblastic) cleavage. While holoblastic cleavage resembles conventional cytokinesis both in vitro and in vivo, the mechanisms underlying meroblastic cleavage have remained poorly understood. Using zebrafish embryos as a model, we show that meroblastic cleavage proceeds through a distinct two-step mechanism. The process begins with the assembly and contraction of a large, arc-shaped actomyosin cable. However, this contractile event alone is insufficient to complete division. A second phase, driven by cadherin-mediated membrane adhesion, is required to invaginate the furrow ridge. Strikingly, this transition depends on mechanical uncoupling of the contractile cable from the surrounding cortex. We demonstrate that such uncoupling arises from an active nematic instability, which both enhances contractility along the cable and generates actin depletion zones that relieve lateral connections. Together, these findings reveal that meroblastic cleavage is governed not by a single actomyosin-based event but by a sequential interplay between cytoskeletal contraction and cadherin-dependent adhesion, highlighting a mechanism fundamentally distinct from canonical cytokinesis.

cell biology↗