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Tomida, K.

Publications and source records attributed to Tomida, K..

3 recordsLinked to original sources

Dual curvature sensing governs cell orientation and curvotaxis

Cells lying in a curved environment can respond to the surface curvature by reorienting their shape. However, whether cells respond to the mean curvature and/or the Gaussian curvature remains largely unexplored. Here, inspired by experimental observations of how ovarian theca cells (TCs) orient themselves on substrates with different curvatures, we propose a theoretical framework for active nematic layers on curved surfaces. In this model, we assume that the nematic directors of the cells respond to both the mean curvature and the Gaussian curvature of the underlying substrate surface. Our theory predicts specific cell orientation patterns on hemicylindrical, hourglass- and dome-like substrates, consistent with experimental observations. In addition, by incorporating a curvotaxis traction, our model successfully recapitulates the experimental observation of TC accumulation at convex regions of hemicylindrical substrates as well as saddle-shaped regions of more complex geometries. Overall, our work reveals the unexpected role of cell curvature sensing in driving collective migration and pattern formation on various substrate curvatures. SIGNIFICANCESubstrate surface curvature is a critical environmental cue that can influence multicellular organization and functions. Yet how cells collectively align and migrate on complex curved surfaces remains unclear. Here, we proposed a hydrodynamic theory of active nematic layers over curved surfaces for contractile theca cells (TCs), where we assume that the nematic directors of cells can respond to both the mean curvature and the Gaussian curvature of the underlying substrates. Our theory predicts distinct cell orientation patterns on hemicylindrical, hourglass- and dome-like substrates, consistent with experimental observations. Furthermore, by introducing curvotaxis traction, our model recapitulates experimentally observed accumulation of TCs at the convex regions of hemicylindrical substrates as well as saddle-shaped regions of more complex geometries. Together, our study provides a simple theoretical framework to unify our understanding of curvature sensing across complex topology, providing insights into geometric control of tissue pattern formation.

biophysics↗

Theca cell mechanosensing and regulation of follicular extracellular matrix during ovarian follicle development

Mammalian folliculogenesis is essential for female hormonal regulation and successful reproduction. While the steroidogenic functions of theca cells (TCs) have been implicated in ovarian diseases and infertility, the physico-structural properties of TCs and their associated extracellular matrix (ECM), or theca matrix, remain poorly understood. Using murine ovaries, we show that a stiff basement membrane (BM) and theca matrix constitute a mechanically instructive niche that modulates TC proliferation and Yes-associated protein (YAP) signalling in secondary follicles. We identify hyaluronic acid (HA) as a key matrix component that is actively secreted by contractile TCs. The HA scaffold, in turn, regulates TC proliferation, YAP signalling and motility, and is required for overall follicle growth. We showed that stiffer substrates enhance YAP nuclear transport in TCs, while mechanical stretch, cell packing, and curvature affect TC proliferation. In addition, TCs exhibit directed migration towards regions of positive curvature. Together, this study reveals a mechanochemical feedback mechanism that establishes TC mechanics and HA as key regulators of theca matrix formation that is essential for mammalian folliculogenesis. SIGNIFICANCEThe structural properties and mechanical functions of the basement membrane and theca cell-matrix encapsulating mammalian ovarian follicles are poorly understood. Our findings reveal that during early stage of follicle development, the basement membrane remains thin and stiff, while the theca cells actively secrete hyaluronic acid in a contractility-dependent manner. The hyaluronic acid scaffold, in turn, regulates theca cell YAP signalling, proliferation and motility that are required for functional growth of follicles. We further showed that the theca cells are mechanosensitive and fine-tune their proliferative capacity and Hippo pathways in response to substrate stiffness, stretch and curvature. Together, our study uncovers mechanoregulatory feedback between theca cells and associated extracellular matrix, offering new insights into environmental control of folliculogenesis in female reproduction.

developmental biology↗

Theca cell mechanics and tissue pressure regulate mammalian ovarian folliculogenesis

The maturation of functional eggs within the ovaries is essential for successful reproduction and organismal functions in mammals. Yet, despite its biological and clinical importance, the underlying mechanisms regulating folliculogenesis remain enigmatic. Here, we report a novel role of the surface-anchoring theca cells (TCs) in regulating follicle growth through mechanical signalling. Direct mechanical measurements reveal that these TCs are highly contractile and exert compressive stress to the follicular interior, potentially through active assembly of fibronectin scaffold around the follicles. Abolishing TC contractility disrupts fibronectin assembly, increases follicle size, and decreases intrafollicular pressure and viscosity. We further reveal that the granulosa cells (GCs) within the follicles exhibit spatial patterns of YAP signalling and proliferation, which appear to be decoupled. Transient manipulation of tissue pressure through bulk follicle compression, laser ablation or pharmacological perturbation of TC contractility leads to changes in GC YAP signalling, proliferation, and oocyte-GC communications, while long term abrogation of TC contractility leads to impaired follicle growth. Altogether, our study unveils the unique role of TC-mediated tissue pressure in ensuring robust mammalian ovarian folliculogenesis.

developmental biology↗