A quantitative pipeline for whole-mount deep imaging and analysis of multi-layered organoids across scales
Year: 2026
Type: article
Abstract: Whole-mount 3D imaging at the cellular scale is a powerful tool for exploring complex processes during morphogenesis. In organoids, it allows examining tissue architecture, cell types, and morphology simultaneously in 3D models. However, cell packing in multilayered organoid tissues hinders both deep imaging and quantification of cell-scale processes. To address these challenges, we developed an experimental and computational pipeline to extract properties at scales ranging from cell to tissue. The experimental module is based on two-photon imaging of immunostained organoids. The computational module corrects for optical artifacts, performs accurate 3D nuclei segmentation and reliably quantifies gene expression. We provide the computational module as a user-friendly Python package called Tapenade, along with napari plugins which enable joint data processing and exploration across scales. We demonstrate the pipeline by quantifying 3D spatial patterns of gene expression and nuclear morphology in gastruloids, revealing how local cell deformations and gene co-expression relate to tissue-scale organization. This quantitative pipeline improves our understanding of gastruloid development, and lays the groundwork for a wide range of multi-layered organoids and tumoroids systems
Source: eLife
Language: English
Subfield: Biophysics
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $2,500
Awards: G1017527968, CenTuri : Centre Turing des Systèmes vivants, G381343574, G381665449, Rheological patterning of embryonic organoids, Integration of biochemical and mechanical signals at cell adhesive contacts during mammalian morphogenesis: a quantitative approach using a minimal self-organized system
OpenAlex ID: W4401669904
