bioRxivCell BiologyPreprint
Microdomes: Micro-engineered Microdome arrays enable standardised and shear-free 3D biology with full-spectrum optical imaging compatibility
Mei Shan CheamiD, Saburnisha Binte Mohamad Raffi, Hui Ting OngiD, Sandra E. GhayadiD, Marion Le GrandiD, Eddy PasquieriD, Phoebe Dunbabin, Kate PooleiD, Jasmine Fei Li ChiniD, Liu Jun, Esra Karatas, Natalie Sheng Jie Lim, Joanne Tze Chin LimiD, Modhura GangulyiD, Alison M. FergusoniD, Véronique AngeliiD, Yusuke ToyamaiD, Gianluca GrenciiD, Anne BéghiniD
Abstract
Three-dimensional cellular models such as organoids and spheroids hold major promise for developmental biology, disease modelling and precision medicine, yet their large-scale production and analysis remain constrained by handling-induced shear stress, sample fragility, positional instability and limited compatibility with advanced imaging workflows. Here, we introduce Microdomes, dense arrays of open-top, dome-shaped microcavities. Each cavity holds a single specimen in its own miniature aquarium, accessed through a narrow apical opening that admits cells, medium, matrix and staining reagents while shielding it from the shear generated during routine pipetting. Each Microdomes chip accommodates more than 100 spheroids or organoids, supporting diverse cell types, co-culture formats and both matrix-free and matrix-embedded culture. All specimens are retained through prolonged culture, repeated medium exchange, fixation and immunostaining. Because every specimen occupies a fixed, addressable position against a thin transparent film, the same spheroid can be relocated and re-imaged over weeks of culture and across microscopes, from array-wide overviews to subcellular details, without transfer, embedding or other perturbation. Microdomes also support AI-based automated segmentation, from whole-spheroid outlines to individual nuclei in 3D, using common image analysis software. Microdomes thereby turn each array into a self-contained quality control unit, providing specimen-level traceability that organoid production pipelines currently lack.
- assay: organoid / primary culture
- research focus: cell type annotation
- research focus: clustering
- research focus: cell-cell communication
- research focus: spatial domain detection
- approach: experimental assay
- Citations
- 0
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