Method Article

Production and Administration of Therapeutic Mesenchymal Stem/Stromal Cell (MSC) Spheroids Primed in 3-D Cultures Under Xeno-free Conditions

DOI:

10.3791/55126

⸱

March 18th, 2017

In This Article

Summary

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The therapeutic potential of mesenchymal stem/stromal cells (MSCs) is well-documented, however the best method of preparing the cells for patients remains controversial. Herein, we communicate protocols to efficiently generate and administer therapeutic spherical aggregates or 'spheroids' of MSCs primed under xeno-free conditions for experimental and clinical applications.

Abstract

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Mesenchymal stem/stromal cells (MSCs) hold great promise in bioengineering and regenerative medicine. MSCs can be isolated from multiple adult tissues via their strong adherence to tissue culture plastic and then further expanded in vitro, most commonly using fetal bovine serum (FBS). Since FBS can cause MSCs to become immunogenic, its presence in MSC cultures limits both clinical and experimental applications of the cells. Therefore, studies employing chemically defined xeno-free (XF) media for MSC cultures are extremely valuable. Many beneficial effects of MSCs have been attributed to their ability to regulate inflammation and immunity, mainly through secretion of immunomodulatory factors such as tumor necrosis factor-stimulated gene 6 (TSG6) and prostaglandin E2 (PGE2). However, MSCs require activation to produce these factors and since the effect of MSCs is often transient, great interest has emerged to discover ways of pre-activating the cells prior to their use, thus eliminating the lag time for activation in vivo. Here we present protocols to efficiently activate or prime MSCs in three-dimensional (3D) cultures under chemically defined XF conditions and to administer these pre-activated MSCs in vivo. Specifically, we first describe methods to generate spherical MSC micro-tissues or 'spheroids' in hanging drops using XF medium and demonstrate how the spheres and conditioned medium (CM) can be harvested for various applications. Second, we describe gene expression screens and in vitro functional assays to rapidly assess the level of MSC activation in spheroids, emphasizing the anti-inflammatory and anti-cancer potential of the cells. Third, we describe a novel method to inject intact MSC spheroids into the mouse peritoneal cavity for in vivo efficacy testing. Overall, the protocols herein overcome major challenges of obtaining pre-activated MSCs under chemically defined XF conditions and provide a flexible system to administer MSC spheroids for therapies.

Introduction

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Mesenchymal stem/stromal cells (MSCs) have shown great potential for various regenerative medicine approaches. MSCs were initially isolated as a stromal component of bone marrow but have since been obtained from numerous other adult tissues, including adipose tissue1,2,3. Interestingly, the main isolation method embraces the remarkable property of MSCs to adhere tightly onto tissue culture plastic in the presence of fetal bovine serum (FBS). Whilst this traditional isolation technique permits easy and rapid expansion of MSCs in two-dimensional (2D) culture, it is also very ar....

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Protocol

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1. MSC Isolation and Expansion

  1. Obtain early passage MSCs from Center for the Preparation and Distribution of Adult Stem Cells (http://medicine.tamhsc.edu/irm/msc-distribution.html)15 as frozen vials. Alternatively, isolate MSCs from bone marrow aspirates following a routine protocol14 and store as frozen vials.
  2. Prepare complete culture medium (CCM), which is minimal essential medium alpha (αMEM) supplemented with 15-20% premium select FBS, 2 mM L-glutamine, and 1x penicillin-streptomycin. Sterilize the medium by ....

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Results

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In the current work, hanging drop cultures were employed to generate compact spherical micro-tissues or 'spheroids' of activated MSCs under XF conditions. The investigational roadmap in Figure 1 depicts that MSCs are encouraged to self-assemble into spheroids when suspended in hanging drops for 72 hr, after which the spheroids, or the CM loaded with sphere-derived therapeutic factors, can be collected and potentially utilized in both research and clinical applications. Th.......

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Discussion

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The optimal MSC for use in some research and clinical applications should be highly activated to maximize their benefit, and preferentially prepared under chemically defined XF conditions to minimize the delivery of potential antigens from xenogeneic medium components such as FBS. In the protocols described here, we have shown methods to 1) activate MSCs in 3D culture by formation of spheroids, 2) achieve the 3D activation of MSCs under XF conditions, 3) evaluate the activation levels of spheroid MSCs in regards to their.......

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Disclosures

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The authors declare they have no competing financial interests.

Acknowledgements

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This work was funded in part by grant P40RR17447 from the National Institute of Health and award RP150637 from the Cancer Prevention and Research Institute of Texas. We would like to thank Dr. Darwin J. Prockop for his support on the project.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
MEM-α (minimal essential medium alpha)ThermoFisher/Gibco12561049; 12561056; 12561072minimal essential medium for preparation of MSC growth medium (CCM)
FBS (fetal bovine serum), premium selectAtlanta BiologicalsS11595; S11510; S11550; S11595-24component of complete culture media for all types of cells
L-glutamineThermoFisher/Gibco25030081; 25030149; 25030164component of complete culture media for all types of cells
Penicillin/StreptomycinThermoFisher/Gibco15070063component of complete culture media for all types of cells
Sterilization Filter Units, 0.22 µm PES membraneMilliporeSigmaSCGPU01RE; SCGPU02RE; SCGPU05RE; SCGPU10RE; SCGPU11REmedia sterilization
150 mm cell culture dishNuncD8554 SIGMAcell culture
Thermo Forma water-jacketed CO2 humidified incubatorThermo FisherModel 3110incubation of cultured cells
Early passage MCSsCenter for the preparation and Distribution of Adult Stem Cells at The Texas A&M Health Science Center College of Medicine Institute for Regenerative Medicine at Scott & WhiteNApreparation of 2D and 3D cultures of MSCs
water bathVWR89501-468warming media to 37 °C
PipettesEppendorf492000904manual liquid handling
Pipete-AidDrummond Scientific Company4-000-300handling sereological pipetes
Costar sterile serological pipet (5, 10, 25 and 50 ml)Corning4487; 4101; 4251; 4490liquid handling
PBS (phosphate buffered saline), pH 7.4ThermoFisher/Gibco10010023; 10010072; 10010031; 10010049cell culture processing
0.25% trypsin/EDTA solutionThermoFisher/Gibco25200056; 25200072; 25200114lifting adherent cells and dispersing cell aggregates
15 ml conical tubeCorning/BD Falcon352097cell centrifugation
50 ml conical tubeCorning/BD Falcon352098cell centrifugation
Eppendor refrigerated centrifugeEppendorf/Fisher ScientificModel 5810Rcell centrifugation
hemocytometerFisher Scientific26716cell counting
trypan blueSigma-AldrichT8154 SIGMAdead cell exclusion during cell counting in hemacytometer
Defined xenofree MSC medium-1 (XFM-1)ThermoFisher/GibcoA1067501Xeno-free media specifically formulated for the growth and expansion of human mesenchymal stem cells
Defined xenofree MSC medium-2 (XFM-2)Stem Cell Technologies5420Defined, xeno-free medium for human mesenchymal stem cells
HSA (Human serum albumin)Gemini800-120Component of xeno-free MSC media
rHSA (recombinant Human serum albumin)Sigma-AldrichA9731 SIGMAComponent of xeno-free MSC media
Total RNA isolation Mini KitQiagen74104Total RNA extraction
QiashredderQiagen79654Sample homogenization prior to total RNA extraction
RNAse-free DNase Set Qiagen79254On-column DNA elimination during total RNA extraction
β-mercaptoethanol Sigma-AldrichM6250 ALDRICHinhibition of RNAses in RLT buffer
VortexVWR97043-562mixing sample
SpectrophotometerBioradNARNA concentration and quality
High capacity cDNA Reverse Transcription KitThermoFisher/Applied Biosystems4368814transcription of total RNA into cDNA
Gene Expression AssaysThermoFisher/Applied Biosystemsvariesprimer/probe combination for real-time PCR
Fast Universal PCR Master MixThermoFisher/Applied Biosystems4352042; 4364103; 4366073; 4367846master mix for real-time PCR reaction
Real-time PCR system (ABI Prism 7900 HT Sequence Detection System)ABI PrizmNAreal-time PCR
1.5 ml centrifuge tubeEppendorf22364111cell centrifugation, sample collection and storage
(-80 °C) freezerThermo FisherModel Thermo Forma 8695sample storage
PGE2 (Prostaglandin E2) ELISA KitR&D SystemsKGE004Bestimation of cytokine concentration in the sample
DMEM (Dulbecco’s modified Eagle medium)ThermoFisher/Gibco10566-016; 10566-024;10566-032macrophage culture media
J774 mouse macrophagesATCCTIB-67mouse macrophage cell line
12-well plateCorning3513in vitro macrophage stimulation
LPS (lipopolysaccharide)Sigma-aldrichL4130in vitro macrophage stimulation
Mouse TNF-a ELISA kitR&D SystemsMTA00Bestimation of cytokine concentration in the sample
Mouse IL-10 (interleukin 10) ELISA kitR&D SystemsM1000Bestimation of cytokine concentration in the sample
RPMI-1640 mediumThermoFisher/Gibco11875-085splenocyte culture media
BALB/c miceThe Jackson Laboratory651in vivo spheroid delivery; splenocyte preparation
Anti-Mouse CD3e Functional Grade PurifiedeBioscience145-2C11in vitro splenocyte stimulation
70 μm strainer Corning352350Splenocyte preparation
Red blood cell lysis solution (1x)Affymetrix eBioscience00-4333removal of red blood cells during splenocyte isolation
Mouse IFN-γ (interferon gamma) ELISA kitR&D SystemsMIF 00estimation of cytokine concentration in the sample
LNCaP prostate cancer cells ATCCCRL-1740study the effect of 3D MSCs on cancer cell lines in vitro
DNA-based cell proliferation assay kitThermoFisherC7026cell number measurement based on DNA content
NaClSigma-AldrichS5150component of lysis reagent
EDTA (ethylenediaminetetraacetic acid)ThermoFisherFERR1021calcium chelator, component of lysis reagent
Rnase AQiagen19101RNA degradation for measurement of DNA
Filter-based multi-mode microplate readerBMG TechnologyNAMicroplate assays (ELISA, cell quantification, etc.)
HBSS (Hanks balanced salt solution), no calcium, no magnesium, no phenol redThermoFisher/Gibco14175079resupsension of MSC spheroids prior to in vivo injections
IsofluraneMWI Vet Supply502017Anesthesia for in vivo injections
Oxygen, compressed gasPraxairNAFor use with isoflurane
Thermo Forma BSL-2 cabinetThermo FisherModel 1385Sterile cell culture
Safety I.V. catheter/needle stiletto, 20 G , 1 inchTerumoSR*FNP2025Delivery of shperoids into peritoneal cavity
Sterile micropipette tipsEppendorfvariesliquid/cells handling

References

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  1. Keating, A. Mesenchymal stromal cells: New directions. Cell Stem Cell. 10 (6), 709-716 (2012).
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  3. Le Bl....

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Tags

Mesenchymal Stem CellsMSC SpheroidsXeno free ConditionsHanging Drop TechniqueConditioned Medium HarvestIntraperitoneal InjectionGene Expression ScreeningAnti inflammatory FactorsPGE2 AssayTSG6 Expression

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