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Method Article

Real-Time Detection and Capture of Invasive Cell Subpopulations from Co-Cultures

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DOI:

10.3791/63512

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March 30th, 2022

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In This Article

Summary

We describe an approach to detect and capture invasive cell subpopulations in real-time. The experimental design uses Real-Time Cellular Analysis by monitoring changes in the electric impedance of cells. Invasive cancer, immune, endothelial or stromal cells in complex tissues can be captured, and the impact of co-cultures can be assessed.

Abstract

Invasion and metastatic spread of cancer cells are the major cause of death from cancer. Assays developed early on to measure the invasive potential of cancer cell populations typically generate a single endpoint measurement that does not distinguish between cancer cell subpopulations with different invasive potential. Also, the tumor microenvironment consists of different resident stromal and immune cells that alter and participate in the invasive behavior of cancer cells. Invasion into tissues also plays a role in immune cell subpopulations fending off microorganisms or eliminating diseased cells from the parenchyma and endothelial cells during tissue remodeling and angiogenesis. Real-Time Cellular Analysis (RTCA) that utilizes impedance biosensors to monitor cell invasion was a major step forward beyond endpoint measurement of invasion: this provides continuous measurements over time and thus can reveal differences in invasion rates that are lost in the endpoint assay. Using current RTCA technology, we expanded dual-chamber arrays by adding a further chamber that can contain stromal and/or immune cells and allows measuring the rate of invasion under the influence of secreted factors from co-cultured stromal or immune cells over time. Beyond this, the unique design allows for detaching chambers at any time and isolating of the most invasive cancer cell, or other cell subpopulations that are present in heterogeneous mixes of tumor isolates tested. These most invasive cancer cells and other cell subpopulations drive malignant progression to metastatic disease, and their molecular characteristics are important for in-depth mechanistic studies, the development of diagnostic probes for their detection, and the assessment of vulnerabilities. Thus, the inclusion of small- or large-molecule drugs can be used to test the potential of therapies that target cancer and/or stromal cell subpopulations with the goal of inhibiting (e.g., cancer cells) or enhancing (e.g., immune cells) invasive behavior.

Introduction

Cell invasion is an important process that allows cells to cross basement membrane barriers in response to environmental cues provided by stromal cells. It is a crucial step during several stages of development for immune responses, wound healing, tissue repair, and malignancies that can progress from local lesions to invasive and metastatic cancers1. Assays developed early on to measure the invasive potential of cell populations typically generate a single endpoint measurement or require pre-labeling of invasive cells2. The integration of microelectronics and microfluidics techniques is now developed to detect different....

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Protocol

The study was reviewed and considered as "exempt" by the Institutional Review Board of Georgetown University (IRB # 2002-022). Freshly harvested bone marrow tissues were collected from discarded healthy human bone marrow collection filters that had been de-identified.

1. New chamber design (Figure 2)

  1. Open a new dual-chamber cell analyzer plate. Set aside the top chamber with electrodes.
  2. Using a milling machine, shave off 2 mm of the U-shaped bottom wells of the cell analyzer plate.
  3. Attach a 2 cm x 7 cm polyethersulfone (PES) membrane with....

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Results

Using the newly designed three-chambered array, invasion of the cells was tested in the presence or absence of stromal cells such as fibroblasts. MDA-MB-231 cell invasion was enhanced when irradiated Swiss 3T3 fibroblasts (J2 strain) were seeded in the bottom chamber, allowing for the exchange of factors between the two cell lines. Interestingly, MDA-MB-231 invasion increased when 3T3-J2 cells were doubled in number (Figure 3A). On the other hand, the invasion rate of an invasive clone of MC.......

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Discussion

We have modified the design of a dual-chambered array to include a third chamber for monitoring cell invasion in real-time in the presence of stromal cells. We have observed distinct effects of co-cultured fibroblasts on invasive and non-invasive cancer cells indicating that the array can be used to distinguish between cancer cell subpopulations that respond differently to factors produced by co-cultured stromal cells. The array was also used to monitor endothelial cell invasion into stromal tissues, a critical step duri.......

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Disclosures

Georgetown University filed a patent related to some of the approaches described in this manuscript. G.M.S, A.W, L.D, and M.P are named as inventors on this application and declare that as a potential conflict of interest.

Acknowledgements

We would like to thank Dr. Alana Welms, Huntsman Cancer Institute, University of Utah, for providing us with the patient-derived xenografts (HCI-010). This work was supported by NIH grants R01CA205632, R21CA226542, and in part, by a grant from Agilent Technologies.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
0.05% Trypsin-EDTAThermofisher25300-054
AdhesiveNorland Optical AdhesiveNOA63
Bovine serum albumin (BSA)SigmaA9418
Cell lifterSarstedt83.1832
Cholera Toxin from Vibrio choleraeThermofisher12585-014
CIM-plateAgilent5665817001Cell analyzer plate
Collagenase from Clostridium histolyticumSigmaC0130
DispaseStemCell7913
DMEMThermofisher11995-065
DMEM-F12Thermofisher11875-093
Fetal Bovine Serum (FBS), Heat InactivatedOmega ScientificFB-12
HEPESThermofisher15630106
Horse serum (HS)Gibco16050-122
Human EGFPeprotechAF-100-15
Human umbilical Vein endothelail cells (HUVEC)LONZA (RRID:CVCL_2959)C-2517A
HUVEC mediaLONZACC-3162
HydrocortisoneSigmaH4001
Insulin Transferrin Selenium Ethanolamine (ITSX) (100x)Thermofisher51500056
Insulin, Human Recombinant, Zinc SolutionSigmaC8052
J2 FibroblastsStemcell (RRID:CVCL_W667)100-0353
LymphoPrepStemcell7851Density gradient medium for the isolation of mononuclear cells
MatrigelCorning354230Basement membrane matrix
MCFDCIS.com cells ( DCIS)RRID:CVCL_5552
MDA-MB-231 cellsRRID:CVCL_0062
Milling machineBridgeport Series 1 Vertical
Phosphate-buffered saline (1x)Thermofisher10010049
Polyethersulfone (PES) membraneSterlitechPCTF029030
RBC lysis solutionStemcell7800
RNeasy Micro KitQiagen74004
RTCA DP analyzerAgilent3X16Dual purpose cell analyzer
TrypsinSigmaT4799

References

  1. Friedl, P., Gilmour, D. Collective cell migration in morphogenesis, regeneration and cancer. Nature Reviews Molecular Cell Biology. 10 (7), 445-457 (2009).
  2. Boyden, S. The chemotactic effect of mixtures of anti....

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