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Method Article

Generation of Lymphocytic Microparticles and Detection of their Proapoptotic Effect on Airway Epithelial Cells

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DOI:

10.3791/52651

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February 20th, 2015

 ,  ,  ,  ,  ,  , 

* These authors contributed equally

In This Article

Summary

Cell membrane–shed microparticles (MPs) are active biological vesicles that can be isolated and their pathophysiological effects investigated in various models. Here we describe a method for generating MPs derived from T lymphocytes (LMPs) and for demonstrating their proapoptotic effect on airway epithelial cells.

Abstract

Interest in the biological roles of cell membrane–derived vesicles in cell–cell communication has increased in recent years. Microparticles (MPs) are one such type of vesicles, ranging in diameter from 0.1 μm to 1 μm, and typically shed from the plasma membrane of eukaryotic cells undergoing activation or apoptosis. Here we describe the generation of T lymphocyte–derived microparticles (LMPs) from apoptotic CEM T cells stimulated with actinomycin D. LMPs are isolated through a multistep differential centrifugation process and characterized using flow cytometry. This protocol also presents an in situ cell death detection method for demonstrating the proapoptotic effect of LMPs on bronchial epithelial cells derived from mouse primary respiratory bronchial tissue explants. Methods described herein provide a reproducible procedure for isolating abundant quantities of LMPs from apoptotic lymphocytes in vitro. LMPs derived in this manner can be used to evaluate the characteristics of various disease models, and for pharmacology and toxicology testing. Given that the airway epithelium offers a protective physical and functional barrier between the external environment and underlying tissue, use of bronchial tissue explants rather than immortalized epithelial cell lines provides an effective model for investigations requiring airway tract tissue.

Introduction

Microparticles (MPs) are biologically active submicron membrane vesicles released following cell activation or apoptosis. MPs are derived from both healthy and damaged cells and are implicated in many physiological and pathological processes.1 MPs have been detected not only in human plasma, but also in inflammatory and apoptotic tissue. The biological utility of cell membrane–derived MPs has been demonstrated in various settings, including cell signalling models and as pharmacological tools.2,3 We previously demonstrated that LMPs derived from T lymphocytes following actinomycin D stimulation (to induce apoptosis) suppress angiogenesis and....

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Protocol

NOTE: Male C57BL/6 mice (5–7 weeks old) are from Charles River Laboratories International, Inc. (St-Constant, Quebec, Canada.) and manipulated according to protocols approved by the CHU Sainte-Justine Animal Care Committee. Mouse bronchial tissue explants provide a good source of primary bronchial epithelial cells for investigating the proapoptotic effects of LMPs on epithelial cells. This protocol describes the in vitro generation of LMPs, as well as a method for detecting apoptotic epithelial cells on LMPs-treated bronchial tissue explants. This protocol consists of 3 sections.

1. LMPs Production and Characterization

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Results

LMPs were characterized with annexin V staining10 by fluorescence-activated cell sorting (FACS) analysis and gated using 1 µm beads in which 97% of MPs (≤1 µm) were annexin-V-Cy5 positive (Figure 1A and 1B). Typically, about 2.5 mg of LMPs were obtained following this protocol. Bronchial tissue explants from C57BL/6 mice were subjected to vehicle and LMPs treatment. Histopathological analysis of bronchial sections revealed the effect of LMPs on the structural integrity of the bronchial epithel.......

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Discussion

MPs are active mediators of intercellular cross talk and their study is promising in many areas of science.11 This study presented a detailed protocol for in vitro large-scale generation of LMPs derived from an apoptotic T cell line. These MPs express a large repertoire of lymphocyte molecules and are biologically implicated in the regulation of cellular and tissue homeostasis. However, LMPs derived from different sources may be biologically different.4,9,12,13

L.......

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Disclosures

The authors have nothing to disclose.

Acknowledgements

This work is supported by grants from the Canadian Institutes of Health Research (178918), Fonds de recherche en santé du Québec – Vision Health Research Network.

....

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
LMPs production and characterization
CEM T cells ATCC CCL-119
X-VIVO 15 medium Cambrex, Walkersville04-744Q
Flask T75Sarstedt83.1813.502
Flask T175Sarstedt83.1812.502
Actinomycin D Sigma Chemical Co.A9415-2mg
PBSLifetechnologies14190-144
0.22 µm filterSarstedt83.1826.001
Annexin-VCy5BD Pharmagen 559933
FACS flow solutionBD Bio-sciences342003
Fluorescent microbeads (1 µm)Molecular Probes T8880
Polysterene counting beads (7 µm)Bangs laboratoriesPS06N/6994
Polypropylene FACS tubesFalcon352058
1 ml pipetFisher13-678-11B
5 ml pipetFalcon357543
25 ml pipetUltidentDL-357551
1.5 ml conical polypropylene micro tubeSarstedt72.690
15 ml conical polypropylene tubeSarstedt62.554.205
50 ml conical polypropylene tubeSarstedt62.547.205
50 ml high speed polypropylene copolymer tubeNalgene3119-0050
250 ml high speed polypropylene bottleBeckman356011
Protein assay (Bradford assay)Bio-Rad Laboratories500-0006
Protein assay standard IIBio-Rad Laboratories500-0007
Test tube 16 x 100VWR47729-576
Test tube 12 x 75Ultident170-14100005B
Cell incubator MandelHeracell 150
Low speed centrifugeIECCentra8R
High speed centrifugeBeckmanAvanti J8
High speed rotor for 250ml bottleBeckmanJLA16.250
High speed rotor for 50ml tubeBeckmanJA30.50
Fow cytometry BD Bio-sciencesFACS Calibur
SpectrophotometerBeckmanSeries 600
Bronchial tissue explants and sections 
C57BL/6 mice (5-7 weeks old)  Charles River Laboratories, Inc. 
Mouse Airway PrimaCell™ System:CHI Scientific, Inc.2-82001
 Rib-Back Carbon Steel Scalpel BladesBecton Dickinson AcuteCare371310#10
Scalpel HandleFine Science Tools Inc. 10003-12#7
phase-contrast inverted microscopeOlympus Optical CO., LTD.   CK2
high O2 gas mixture VitalAire Canada Inc.
modular incubator chamberBillups-Rothenberg Inc.MIC-101
MaxQ 4000 incubated orbital shakerBarnstead Lab-Line, SHKA4000-7
12-well tissue culture plateBecton Dickinson and Company353043
Plastic tissue culture dishes (100 mm)Sarstedt, Inc.83.1802
Surgical scissorsFine Science Tools Inc. 14060-09Straight, sharp, 9cm longth
Half-curved Graefe forcepsFine Science Tools Inc. 11052-10
humidified CO2 incubatorMandel Scientific Company Inc. SVH-51023421
 Histopathological examination 
formalin formaldehydeSigma-Aldrich, Inc. HT5011
paraffinFisher scientific  International, Inc.T555
ethyl alcoholMerck KGaA, DarmstadtEX0278-1
 glutaraldehyde Sigma-Aldrich, Inc. G6403
CacodylateSigma-Aldrich, Inc. 31533
microscope slidesVWR Scientific Inc. 48300-02525x75 mm
XyleneFisher scientific  International, Inc.X5-4
Mayer's hematoxylinSigma-Aldrich, Inc. MHS16Funnel with filter paper  
HCl Fisher scientific  International, Inc.  A144s-500
eosin Sigma-Aldrich, Inc. HT110116Funnel with filter paper  
Permount™ Mounting MediumThermo Fisher Scientific Inc. SP15-100
glass coverslipsurgipath medical industries, Inc.8450324×24 #1 
TUNEL detection kitIn Situ Cell Death Detection, POD11 684 817 910
ovenDespatch Industries Inc.LEB-1-20
rotary MicrotomeLeica Microsystems Inc.RM2145
filter paperWhatman International Ltd.1003150#3
MicroscopeNikon Imaging Japan Inc.E800
staining dish completeWheaton Industries, Inc.900200including dish, rack, cover
1.5 ml eppendorf tubeSarstedt Inc. 72.6939x10 mm
Orbital and Reciprocating Water BathExpotechUSAORS200
phosphate buffered saline  GIBCO14190-144
fume hoodNicram RD Service3707E

References

  1. Tushuizen, M. E., Diamant, M., Sturk, A., Nieuwland, R. Cell-derived microparticles in the pathogenesis of cardiovascular disease: friend or foe. Arterioscler Thromb Vasc Biol. 31 (1), 4-9 (2011).
  2. Martinez, M. C., Tual-Chalot, S., Leonetti, D., Andriantsitohaina, R.

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