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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.
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.
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....
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.
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 (
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.......
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.
....Name | Company | Catalog Number | Comments |
10 mM HEPES Buffer | Gibco | 15630080 | |
100x Antibiotic-Antimycotic | Gibco | 15240-096 | |
100x Glutamax | Life Technologies | 35050-061 | Glutamine supplement |
100x Insulin-Transferrin-Selenium (ITS) | Life Technologies | 51500-056 | |
100x Penicillin/Streptomycin (Pen/Strep) | Sigma | P4333 | |
10x DMEM | Sigma | D2429 | |
50 mL/0.2 µm filter flask | Fisher | #564-0020 | |
Amphotericin B | Life Technologies | 15290-018 | |
bFGF | Sigma | F0291 | |
BSA Solution (32%) | Sigma | #A9576 | |
Cholera Toxin | Sigma | C8052 | |
CO2-Independent Medium | Gibco | 18045-088 | |
Collagenase A | Sigma | C2139 | |
Deoxyribonuclease I from bovine pancreas (DNase) | Sigma | D4263 | |
DMEM with 4500 mg/L glucose, sodium pyruvate, and sodium bicarbonate, without L-glutamine, liquid, sterile-filtered, suitable for cell culture | Sigma | D6546 | Common basal medium |
D-MEM/F12 | Life Technologies | #10565-018 | Basal cell medium |
Dulbecco's Phosphate Buffered Saline (D-PBS)Â | Sigma | #D8662 | PBS |
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 | #354230 | Basement Extracellular Matrix (BECM) |
NaOH (1 N) | Sigma | S2770 | |
Rat Tail Collagen I | Corning | 354236 | |
RPMI-1640 media | Fisher | SH3002701 | |
Trypsin | Life Technologies | 27250-018 |
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