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Biology subjects

van Leen, E.

Publications and source records attributed to van Leen, E..

2 recordsLinked to original sources

Morphodynamic domains enable integration of live morphometrics and spatial transcriptomics

Tissue development emerges from the coordinated behaviors of thousands of cells, orchestrated by gene regulatory networks. Recent methodological advances now enable high-resolution live imaging of cell- and tissue-scale dynamics and the construction of spatially resolved gene expression atlases. However, quantitatively linking these modalities remains a central challenge, limiting our ability to understand how gene regulatory networks drive cell- and tissue-scale behaviors. Here, using the Drosophila thorax epithelium as a model system, we introduce an analytical and computational framework based on tissue morphodynamic domains: regions defined by coherent cell and tissue dynamics extracted from live imaging morphometrics. Integrating morphodynamic domains with spatial transcriptomics enables the inference of gene regulatory networks associated with distinct spatial cell- and tissue-level behaviors. Statistical cross-scale analyses further allow the interrogation and validation of gene function, confirming or revealing regulators of specific morphogenetic dynamics. In particular, our framework uncovers a role for the Toll-like receptor Tollo in modulating tissue flow, contraction, and apoptosis. Together, our work establishes a framework that integrates spatial transcriptomics with quantitative, multiscale live morphometrics, providing a generalizable strategy to probe and understand developmental processes.

developmental biology↗

Tissue mechanics and systemic signaling safeguard epithelial tissue against spindle misorientation.

Multicellular organisms possess conserved safeguard mechanisms that ensure the maintenance of tissue integrity. Exploring these mechanisms has proven instrumental in understanding how tissues robustly develop and prevent tumor initiation. Here, we investigate how epithelial tissues preserve their architecture and cell number in the face of spindle mis-orientation. Spindle mis-orientation, due to the lack of spindle pulling forces, centrosomes, or mitotic rounding, can cause epithelial cells to be mispositioned within or outside the tissue, leading to significant cell loss. By inducing spindle mis-orientation in Drosophila epithelial tissue, we first found that acentrosomal microtubules and cell contractility prevent excessive epithelial cell loss by enabling mispositioned cells to reintegrate into the epithelium. However, this mechanism alone is insufficient to maintain the total epithelial cell number. We uncovered that epithelial mechanics and cell size sensing monitor and compensate for epithelial cell loss predominantly by reducing physiological apoptosis through Hippo/YAP signaling. Lastly, we found that systemic TNF signaling protects the organism by eliminating potentially harmful non-reintegrating cells. Overall, our results delineate the complementary roles of mechanics and systemic signaling in controlling cell number and position at both tissue and organismal levels.

developmental biology↗