Method Article

Generating Free-floating Normal Human Epithelial-Fibroblast Spheroid Co-Cultures

DOI:

10.3791/68440

July 3rd, 2025

In This Article

Summary

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Here, we present a simple and very practical but reliable protocol for direct spheroidal co-cultivation of human lung epithelial cells and fibroblasts without relying on a matrix.

Abstract

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Three-dimensional (3D) culture systems have become increasingly popular due to their ability to reproduce natural cell properties and architectures, thus mimicking tissue-like structures in vitro. Among these models, the culture of spherical cell aggregates (so-called spheroids) embedded in a semi-solid extracellular matrix (ECM) represents an advanced near-in vivo cell culture model, as it allows for different functional cell states as a result of cell-cell and cell-ECM interactions, as well as oxygen and nutrient gradients. Because spheroids are technically less demanding and relatively inexpensive to obtain, they are frequently used in drug screening and toxicity testing, enabling high-content screening for testing new drugs in the preclinical phase. For this purpose, 3D structures of various tumors are predominantly recreated. At the same time, Matrigel is currently one of the most widely used ECMs and is considered the gold standard in spheroid and organoid cultivation, although this is a 3D matrix based on mouse experiments, the extraction of which- like animal testing in general-is associated with major ethical concerns. Here, we present a matrix-free protocol for direct spheroidal co-cultivation of human bronchial epithelial cells and fibroblasts, which can be considered as an optimized co-cultivation method, especially concerning epithelial-fibroblast communication and interactions within the respective spheroids, without relying on an (animal-based) carrier matrix. By establishing these free-floating epithelial-fibroblastoid spheroid co-cultures as a patient-oriented in vitro platform to model normal (lung) tissue toxicities of cancer therapeutic approaches, not only a reduction in the number of experimental animals but also an adequate and meaningful replacement of corresponding animal experiments can be achieved.

Introduction

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Two-dimensional (2D) cell cultures, in which flat monolayer cells are cultured, expanded, and then plated for cell-based research assays, remain an easy, convenient, cost-effective, and widely used method for standard preclinical screening procedures1,2. To study the interactive (paracrine) crosstalk between various types of cells in vitro, a conditioned medium from one cell type for stimulation of another cell type can be used. Additionally, various co-culture methods emerged, e.g., indirect methods, when co-cultured cells are physically separated using a microporous membrane. These 'Transwell sy....

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Protocol

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All steps are performed under sterile conditions (Biosafety cabinet). For the media compositions used in this study, refer to Table 1.

1. Preparation of experimental material

  1. Culture and expand human normal lung epithelial cells (HBEC3-KT) on standard plastic cell culture dishes (T75 flasks) in normal epithelial growth medium using a standard incubator13 (see Table 1).
    NOTE: For improved growth, the medium can be additionally supplemented with 10% fetal calf serum (FCS).
  2. Culture human fibroblasts (HS-5) in RPMI Medium supplemented with 10....

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Results

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This simple protocol enables the matrix-free spheroidal co-cultivation of human bronchial epithelial cells and fibroblasts in combination with ultra-low attachment plates (Figure 1A). During the cultivation process, more complex lung spheroids gradually form from the initially generated spheroids, with the efficient generation of different epithelial and fibroblastic structures representing direct cellular interactions as revealed by morphological analyses using live cell imaging (

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Discussion

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3D cell culture models have been proposed to bridge the gap between 2D cultures and in vivo studies, as this type of (co-) culture better mimics the physiological, morphological, and pathological properties present in vivo because more in vivo-like cell-cell interactions, cell-ECM interactions, responses to stimuli, gene expression, protein expression, and differentiation are present17,18. In addition to the numerous and sometimes very .......

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Disclosures

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The authors state that there are no personal or institutional conflicts of interest.

Acknowledgements

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We thank Mohammed Benchellal, Eva Gau, Sabine Senkel, and Olga Kruse for their excellent technical assistance. This work was supported by the Federal Ministry of Education and Research (BMBF) (LuOrgNTT: 16LW0293 to D.K., SeniRad: 02NUK086C to V.J., D.K.) and by the DFG Research Training Group 2762.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
10 mL sterile serological pipettes ThermoFischer170356NNunc sterile serological pipettes, or equivalent
15 mL conical tubeCorning430052or equivalent
37 °C/ 5% CO2 humidified  incubator
5 mL sterile serological pipettes ThermoFischer170355NNunc sterile serological pipettes, or equivalent
50 mL conical tubeCorningCLS430829or equivalent
ATRA (All-Trans Retinoic Acid)StemCell TechnologiesCat#7226250 nM
B-27 Supplement (50x), ThermoFischer/GibcoCat#175040441x
BD Rhapsody WTA Amplification KitBD BioscienceCat#633801use according to the manufacturer's instructions
Biosafety cabinet
Bovine Serum AlbuminRocheCat#BSAVHS-RO0.4% (v/v)
Cell StrainerCorning352350Falcon 70 µm Cell Strainer, White, Sterile, Individually Packaged
CentrifugeEppendorfhttps://www.fishersci.com/shop/products/eppendorf-5804-series-centrifuge-rotor-packages-9/p-4119001e.g., Eppendorf Centrifuge 5804 - Benchtop Centrifuge
DMEM/F12InvitrogenCat#11330-032500 mL
DNase I, RNase-free (1 U/μL)ThermoFischerCat#EN0521100 U/mL 
EDTA (0,5 M), pH 8,0, RNase-freeThermoFischerAM9260G2 mM
Eppendorf Research plus 12 channel multichannel pipette Eppendorfe.g., #3125000044 (10–100 µL) or #3125000060 (30–300 µL)
Fetal calf serumThermoFischer/GibcoCat#A525670110% (v/v)
HBEC3-KT ATCCCRL-4051human normal lung epithelial cell line 
Heparin Solution (0.2%)StemCell TechnologiesCat#79800.8 mL
Hoechst 33342 ThermoFischerCat#H13991 µg/mL
HS-5 ATCCCRL-3611human stromal fibroblasts
Hu Recom FGF-10 (KGF-2) ACFStemCell TechnologiesCat#78173.110 ng/mL
Hu Recom FGF-7 (KGF) ACF StemCell TechnologiesCat#78186.110 ng/mL
Human Single-Cell Multiplexing KitBD BioscienceCat#633781use according to the manufacturer's instructions
Hydrocortisin Stock Solution StemCell TechnologiesCat#79260.5 mL per 500 mL
Laduviglusib (CHIR-99021)Biozol/SelleckchemCat#S12633 µM
L-Ascorbic acidSigma-AldrichCat#A9290250 µg/mL
MicroscopeZEISS
MonothioglycerolSigma-AldrichCat#M61450.4 µM
N-2 Supplement (100x)ThermoFischer/GibcoCat#175020481x
Neubauer counting chamberMerckBR718605e.g., BRAND counting chamber BLAUBRAND Neubauer pattern
Normal goat serumThermoFischerCat#318732 % (v/v) in PBS
NP-40Merck/MilliporeCat#492016NP-40-Alternative, 1 %
PAS Staining KitSigma AldrichCat#1016460001use according to the manufacturer's instructions
PBSThermoFischerCat#100100231x
Penicillin-Streptomycin (10.000 U/mL), 100xThermoFischer/GibcoCat#151401221x
PFAThermoFischerCat#J61899.AKParaformaldehyd, 4 % in PBS
PneumaCult Airway Organoid Differentiation Medium (ODM)StemCell TechnologiesCat#05060PneumaCult Airway Organoid Basal Medium (#05061, 360 mL) and PneumaCult Airway Organoid Differentiation Supplement* (#05063, 40 mL)
PneumaCult Ex Plus MediumStemCell TechnologiesCat#5040Kit consisting of PneumaCult-Ex Plus Basal Medium (#05041, 490 mL ) and PneumaCult-Ex Plus 50X Supplement*(#05042, 10 mL)
Protease inhibitor cocktailMerck/RocheCat#46931320011 tab/10 mL
Rhapsody cDNA KitBD BioscienceCat#633773use according to the manufacturer's instructions
RPMI 1640 MediumThermoFischer/GibcoCat#11875093500 mL
Sodium ChlorideMerck/Sigma-AldrichS9625150 mmol/L
Sodium CitrateMerck/Sigma-AldrichCat#1613859-1G0.10%
Sodium DeoxycholateMerck/Sigma-AldrichCat#309700.50%
Sodium Dodecyl Sulfate Merck/Sigma-AldrichCat#116672890010.10%
Sterile reagent reservoir for multichannel micropipette (e.g., 60 ml)ThermoFischer9510037or equivalent
TC-Platte 96well BIOFLOAT a 4 StückSarstedt (or facellitate)83.3925.400 (or F202003)ultra-low attachment plate
Tris/HClThermoFischerCat#AM9855G50 mmol/L , pH 8
Triton X-100Sigma-AldrichCat#X100-5ML0.05 % 
Trypan Blue Stain (0.4%)ThermoFischerCat#152500611/5 (v/v) with NGM
TrypLEThermoFischerCat#126040131x
Trypsin-EDTA (0.5 %)ThermoFischerCat#154000540.05 % Trypsin-EDTA (TE) solution aseptically diluted to 1X using phosphate buffered saline (without calcium and magnesium)
WST-1 reagentCELLPRO-RO, RocheCat#5015944001cell proliferation reagent 

References

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  1. Rasouli, M., Safari, F. Principles of indirect co-culture method using Transwell. Methods Mol Biol. , (2024).
  2. Fontoura, J. C., et al. Comparison of 2D and 3D cell culture models for cell growth, gene expression and drug resistance. Mater Sci Eng C.

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Tags

3D Cell CultureSpheroid Co CultureEpithelial Fibroblast SpheroidsMatrix Free SpheroidsHuman Bronchial EpithelialFibroblast Co CultureCell Cell InteractionsTissue MimicryDrug ScreeningAnimal Free Model
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