Drost & Clevers (2018)
Organoids in cancer research. Nature Reviews Cancer 18:407–418. doi:10.1038/s41568-018-0007-6
View on DOIHow to image 3D organoids and tumoroids with the EVOS M5000 and EVOS M7000. Peer-reviewed papers linked, workflow notes for UK labs.
Organoids and tumoroids are 3D, often 100–500 µm in diameter, and embedded in Matrigel or similar extracellular matrices. That changes what you need from a microscope:
| Workflow | Best EVOS | Why |
|---|---|---|
| Fixed organoid fluorescence imaging | EVOS M5000 | 4-colour LED, Z-stacking, publication image export |
| Live organoid time-lapse | EVOS M7000 | On-stage incubation, multi-well automation, long-term imaging |
| High-throughput organoid/tumoroid screening | EVOS M7000 / CellInsight CX7 | Plate automation and quantitative analysis |
| Budget 3D cell cluster checks | EVOS M3000 | 2-channel fluorescence + phase contrast for routine morphology |
This paper describes a modular culture platform combined with longitudinal brightfield and fluorescence imaging to track organoid growth over days. The emphasis on automation and repeated imaging maps directly to the EVOS M7000's plate-based time-lapse strengths.
What did the modular platform achieve for organoid culture? It combined automated organoid culture with longitudinal brightfield and fluorescence imaging to track organoid growth over several days.
How does the EVOS M7000 fit this longitudinal organoid workflow? The EVOS M7000 supports automated multi-position time-lapse imaging with on-stage environmental control, matching the platform’s need for repeated brightfield and fluorescence capture.
What did the modular platform achieve for organoid culture? It combined automated organoid culture with longitudinal brightfield and fluorescence imaging to track organoid growth over several days.
How does the EVOS M7000 fit this longitudinal organoid workflow? The EVOS M7000 supports automated multi-position time-lapse imaging with on-stage environmental control, matching the platform’s need for repeated brightfield and fluorescence capture.
The study uses advanced time-lapse imaging and image analysis to follow morphogenesis in human early brain organoids. High-resolution Z-stack and time-lapse data were central to tracking developmental dynamics.
What did the study reveal about early brain organoid morphodynamics? It used advanced time-lapse imaging to follow morphogenesis in human early brain organoids, revealing developmental dynamics driven by high-resolution Z-stack and time-lapse data.
How would the EVOS M7000 support brain organoid time-lapse imaging? The EVOS M7000 is suited to long-term live Z-stack acquisition, enabling developmental-stage tracking of brain organoids over time, while the EVOS M5000 can capture fixed fluorescence panels.
What did the study reveal about early brain organoid morphodynamics? It used advanced time-lapse imaging to follow morphogenesis in human early brain organoids, revealing developmental dynamics driven by high-resolution Z-stack and time-lapse data.
How would the EVOS M7000 support brain organoid time-lapse imaging? The EVOS M7000 is suited to long-term live Z-stack acquisition, enabling developmental-stage tracking of brain organoids over time, while the EVOS M5000 can capture fixed fluorescence panels.
Describes an imaging pipeline for intestinal organoids that combines brightfield and fluorescence with automated segmentation. The goal is rapid, plate-compatible quality control and quantitative morphometry.
What did the intestinal organoid imaging pipeline deliver? It combined brightfield and fluorescence imaging with automated segmentation for rapid, plate-compatible quality control and quantitative morphometry of human intestinal organoids.
How does the EVOS M7000 fit this high-throughput organoid pipeline? The EVOS M7000 offers multi-well plate scanning, brightfield and fluorescence channels, and built-in confluence and counting tools that align with the pipeline’s throughput and QC goals.
What did the intestinal organoid imaging pipeline deliver? It combined brightfield and fluorescence imaging with automated segmentation for rapid, plate-compatible quality control and quantitative morphometry of human intestinal organoids.
How does the EVOS M7000 fit this high-throughput organoid pipeline? The EVOS M7000 offers multi-well plate scanning, brightfield and fluorescence channels, and built-in confluence and counting tools that align with the pipeline’s throughput and QC goals.
Uses multispectral 3D live imaging of organoids to screen fluorescent probes. The paper highlights the value of 3D optical sectioning and multi-channel fluorescence for translational screening.
What did the multispectral 3D platform enable for fluorescence-guided surgery? It enabled multispectral 3D live imaging of organoids to screen fluorescent probes, demonstrating the value of optical sectioning and multi-channel fluorescence for translational probe development.
How does the EVOS M5000 support 3D organoid probe screening? The EVOS M5000 provides four-channel LED fluorescence and Z-stack optical sectioning, making it suitable for 3D organoid probe screening at moderate depth.
What did the multispectral 3D platform enable for fluorescence-guided surgery? It enabled multispectral 3D live imaging of organoids to screen fluorescent probes, demonstrating the value of optical sectioning and multi-channel fluorescence for translational probe development.
How does the EVOS M5000 support 3D organoid probe screening? The EVOS M5000 provides four-channel LED fluorescence and Z-stack optical sectioning, making it suitable for 3D organoid probe screening at moderate depth.
Demonstrates long-term live imaging of mammary organoids by light-sheet microscopy, emphasising low phototoxicity and deep 3D coverage for developmental studies.
What did the mammary organoid study demonstrate about live imaging? It demonstrated long-term live imaging of mammary organoids by light-sheet microscopy, highlighting low phototoxicity and deep 3D coverage for developmental studies.
How does the EVOS platform complement light-sheet mammary organoid imaging? While light-sheet remains the gold standard for deep live organoid imaging, the EVOS M7000 can be used for parallel plate-screening and validation, and the EVOS M5000 for routine fluorescence QC.
What did the mammary organoid study demonstrate about live imaging? It demonstrated long-term live imaging of mammary organoids by light-sheet microscopy, highlighting low phototoxicity and deep 3D coverage for developmental studies.
How does the EVOS platform complement light-sheet mammary organoid imaging? While light-sheet remains the gold standard for deep live organoid imaging, the EVOS M7000 can be used for parallel plate-screening and validation, and the EVOS M5000 for routine fluorescence QC.
Presents signal correction, segmentation and quantification for multilayered organoid and tumoroid systems. The workflow requires reliable Z-stack data as input.
What did the whole-mount pipeline provide for organoid analysis? It provided signal correction, segmentation, and quantification workflows for multilayered organoid and tumoroid systems, requiring reliable Z-stack data as input.
How do EVOS systems feed into this whole-mount organoid pipeline? The EVOS M5000 or M7000 can acquire routine Z-stacks that feed into the downstream image-analysis pipeline, with the EVOS M7000 preferred for higher-throughput or multi-position datasets.
What did the whole-mount pipeline provide for organoid analysis? It provided signal correction, segmentation, and quantification workflows for multilayered organoid and tumoroid systems, requiring reliable Z-stack data as input.
How do EVOS systems feed into this whole-mount organoid pipeline? The EVOS M5000 or M7000 can acquire routine Z-stacks that feed into the downstream image-analysis pipeline, with the EVOS M7000 preferred for higher-throughput or multi-position datasets.
For 200–400 µm organoids, capture Z-stacks at 2–5 µm steps. Use transmitted light or low-intensity fluorescence to minimise phototoxicity during live imaging. EVOS M5000 and M7000 both support Z-stacking without a confocal pinhole.
Typical panel: DAPI/Hoechst (nuclei), GFP (reporter), RFP/mCherry (second marker), Cy5 (deep marker). EVOS LED cubes avoid laser alignment and warm-up, which helps routine labs.
Organoids need stable temperature, humidity and CO₂. The EVOS M7000 on-stage chamber supports this; for very long experiments consider an incubator imager such as the zenCELL owl as a complementary platform.
Yes. The EVOS M5000 is a four-colour LED fluorescence inverted microscope with transmitted light and Z-stacking, making it well suited to fixed and live organoid/tumoroid imaging up to several hundred micrometres deep. For automated multi-well plate organoid assays over hours or days, the EVOS M7000 adds on-stage incubation and time-lapse automation.
The EVOS M7000 is the better choice for live organoid time-lapse because it supports on-stage incubation, automated multi-position acquisition and long-term imaging in multi-well plates. The EVOS M5000 can capture still Z-stacks of live organoids but lacks the environmental control of the M7000.
Common organoid/tumoroid labels use DAPI or Hoechst for nuclei, GFP for reporter proteins or lineage tracing, RFP/mCherry for second reporters, and Cy5 for deeper targets. The EVOS M5000 and M7000 cover these four LED channels without laser alignment, simplifying routine organoid fluorescence workflows.
No. The papers above are independent peer-reviewed studies that used a range of optical platforms (wide-field, light-sheet, confocal). We map their imaging requirements to the EVOS M5000 and EVOS M7000 specifications so UK labs can choose the right Thermo Fisher workflow without over-specifying.
Compare organoid microscopes → View EVOS systems on Thermo Fisher UK →
Organoids in cancer research. Nature Reviews Cancer 18:407–418. doi:10.1038/s41568-018-0007-6
View on DOIA living biobank of breast cancer organoids captures disease heterogeneity. Cell 172:373–386. doi:10.1016/j.cell.2017.11.010
View on DOITubuloids derived from adult human kidney tissue for nephrotoxicity testing. Nature Biotechnology 37:303–313. doi:10.1038/s41587-019-0048-z
View on DOIA rectal cancer organoid platform to study individual responses to chemoradiation. Nature Medicine 26:1605–1611. doi:10.1038/s41591-020-1049-2
View on DOIThe EVOS M5000 handles brightfield and fluorescence imaging of organoids and tumoroids; larger 3D structures may benefit from confocal or light-sheet systems.
Yes for small tumoroids and 2D/3D monolayers; thick organoids benefit from Z-stacking and deconvolution.
Common stains include live/dead dyes, EdU/BrdU proliferation markers, F-actin, and organ-specific markers such as E-cadherin or CK8.
Use software with object segmentation, such as EVOS onboard analysis, Fiji or high-content platforms, to track area, diameter and sphericity over time.
The cited papers use peer-reviewed imaging workflows compatible with EVOS M5000; they are curated for organoid and tumoroid researchers rather than direct endorsements.
Which microscope platforms are discussed? This page covers benchtop fluorescence and high-content screening systems such as the EVOS M3000, M5000, M7000, S1000 and CellInsight CX7.
Are the papers peer-reviewed? Where possible we link to peer-reviewed publications in journals such as Nature Communications, Scientific Reports, iScience and Molecular Brain, plus preprints on bioRxiv.
Why do these papers matter for UK labs? They show how modern imaging platforms can generate quantitative, reproducible data for disease models, drug discovery and spatial biology workflows.