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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

This protocol discusses an approach for generating epithelial organoids from primary normal and tumor mammary tissue through differential centrifugation. Furthermore, instructions are included for three-dimensional culturing as well as immunofluorescent imaging of embedded organoids.

Abstract

Organoids are a reliable method for modeling organ tissue due to their self-organizing properties and retention of function and architecture after propagation from primary tissue or stem cells. This method of organoid generation forgoes single-cell differentiation through multiple passages and instead uses differential centrifugation to isolate mammary epithelial organoids from mechanically and enzymatically dissociated tissues. This protocol provides a streamlined technique for rapidly producing small and large epithelial organoids from both mouse and human mammary tissue in addition to techniques for organoid embedding in collagen and basement extracellular matrix. Furthermore, instructions for in-gel fixation and immunofluorescent staining are provided for the purpose of visualizing organoid morphology and density. These methodologies are suitable for myriad downstream analyses, such as co-culturing with immune cells and ex vivo metastasis modeling via collagen invasion assay. These analyses serve to better elucidate cell-cell behavior and create a more complete understanding of interactions within the tumor microenvironment.

Introduction

The ability to model epithelial cells in vitro has been the foundation of modern biomedical research because it captures cellular features that are not accessible in vivo. For instance, growing epithelial cell lines in a two-dimensional plane can provide an assessment of the molecular changes that occur in an epithelial cell during proliferation1. Furthermore, measuring the dynamic regulation between signaling and gene expression is limited in in vivo systems2. In cancer research, cancer epithelial cell line modeling has enabled the identification of molecular drivers of disease progression and....

Protocol

All mouse tissue utilized in this manuscript has been ethically collected in accordance with the Institutional Animal Care and Use Committee (IACUC) regulations and guidelines of the University of Texas Southwestern Medical Center. Likewise, all the patients consented prior to tissue donation under the oversight of an Institutional Review Board (IRB), and the samples were deidentified.

NOTE: This protocol describes the generation of organoids from primary tissue.

Representative Results

The images featured in Figure 1 provide an example of wild-type and tumorous mammary epithelial organoids from human and mouse tissues. An at-a-glance illustration of the method for isolating epithelial organoids through differential centrifugation is provided in the cartoon workflow in Figure 1A, showing that primary tissues from different species can be processed in near-identical ways while yielding epithelial tissue as shown in the brightfield images (

Discussion

Different methods have been described in the literature to generate tumor organoids. This protocol highlights a method for generating tumor organoids directly from the tumor without passaging. Using this method, tumor organoids are producible within hours of initiating the procedure and generate close to 100% viable organoids compared to 70% reported in the literature31. In comparison, other methods require serial passaging of cells into organoids over several weeks. Thus, the downstream applicati.......

Acknowledgements

This study was supported by funding provided by METAvivor, the Peter Carlson Trust, Theresa's Research Foundation, and the NCI/UTSW Simmons Cancer Center P30 CA142543. We acknowledge the assistance of the University of Texas Southwestern Tissue Management Shared Resource, a shared resource at the Simmons Comprehensive Cancer Center, which is supported in part by the National Cancer Institute under award number P30 CA142543. Special thanks to all members of the Chan Lab.

....

Materials

NameCompanyCatalog NumberComments
10 mM HEPES BufferGibco 15630080
100x Antibiotic-Antimycotic Gibco 15240-096
100x GlutamaxLife Technologies 35050-061Glutamine supplement
100x Insulin-Transferrin-Selenium (ITS) Life Technologies 51500-056
100x Penicillin/Streptomycin (Pen/Strep)Sigma P4333
10x DMEMSigma D2429
50 mL/0.2 µm filter flaskFisher #564-0020
Amphotericin BLife Technologies 15290-018
bFGFSigmaF0291
BSA Solution (32%)Sigma #A9576
Cholera Toxin Sigma C8052
CO2-Independent Medium Gibco18045-088
Collagenase A Sigma C2139
Deoxyribonuclease I from bovine pancreas (DNase)SigmaD4263
DMEM with 4500 mg/L glucose, sodium pyruvate, and sodium bicarbonate, without L-glutamine, liquid, sterile-filtered, suitable for cell cultureSigmaD6546Common basal medium
D-MEM/F12 Life Technologies #10565-018Basal cell medium
Dulbecco's Phosphate Buffered Saline (D-PBS) Sigma#D8662PBS
Fetal bovine serum (FBS)Sigma #F0926
Gentamicin Life Technologies #15750-060
Human epidermal growth factor (EGF)Sigma E9644
Hydrocortisone Sigma H0396
Insulin Sigma #I9278
Matrigel Corning #354230Basement Extracellular Matrix (BECM)
NaOH (1 N)Sigma S2770
Rat Tail Collagen ICorning 354236
RPMI-1640 mediaFisher SH3002701
Trypsin Life Technologies 27250-018

References

  1. Ghandi, M., et al. Next-generation characterization of the cancer cell line encyclopedia. Nature. 569 (7757), 503-508 (2019).
  2. Roarty, K., Echeverria, G. V. Laboratory models for investigating breast ....

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Keyword Extraction Epithelial OrganoidsMammary TissueMouseHumanTumorNormalPassagingDifferential CentrifugationCollagenMatrixInvasionMammary Fat PadInguinalThoracicCollagenaseBenchtop Shaking IncubatorBasal Medium

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