Summary

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

Published: February 20, 2015
doi:

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 inhibit endothelial cell survival and proliferation.4,5 The antiangiogenic effects of LMPs may vary significantly depending on the stimuli used to activate T lymphocytes in vitro.6

The airway epithelium functions as a protective physical and functional barrier. Increased numbers of T lymphocytes in the airway can contribute to cell damage and airway inflammation.7 We have shown that LMPs induce apoptosis of human bronchial epithelial cells,8 which indicated LMPs may change barrier function of bronchial epithelium in vivo. Apoptotic cells can be identified using the TUNEL method, which detects in situ DNA fragmentation.

The overall goal of this protocol is to illustrate the in vitro production of LMPs from a T lymphocyte cell line, and to demonstrate their proapoptotic effect on airway epithelial cells. In situ cell death detection demonstrated that LMPs strongly induce airway bronchial epithelial cell death, suggesting that LMPs-mediated injury to the airway epithelium may impact barrier function of the damaged epithelium.

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 LM…

Representative 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 b…

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…

Declarações

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.

Materials

LMPs production and characterization
CEM T cells  ATCC  CCL-119
X-VIVO 15 medium  Cambrex, Walkersville 04-744Q
Flask T75 Sarstedt 83.1813.502
Flask T175 Sarstedt 83.1812.502
Actinomycin D  Sigma Chemical Co. A9415-2mg
PBS Lifetechnologies 14190-144
0.22µm filter Sarstedt 83.1826.001
Annexin-VCy5 BD Pharmagen  559933
FACS flow solution BD Bio-sciences 342003
Fluorescent microbeads (1 um) Molecular Probes  T8880
Polysterene counting beads (7 um) Bangs laboratories PS06N/6994
Polypropylene FACS tubes Falcon 352058
1 ml pipet Fisher 13-678-11B
5 ml pipet Falcon 357543
25 ml pipet Ultident DL-357551
1,5 ml conical polypropylene micro tube Sarstedt 72.690
15 ml conical polypropylene tube Sarstedt 62.554.205
50 ml conical polypropylene tube Sarstedt 62.547.205
50 ml high speed polypropylene copolymer tube Nalgene 3119-0050
250 ml high speed polypropylene bottle Beckman 356011
Protein assay (Bradford assay) Bio-Rad Laboratories 500-0006
Protein assay standard II Bio-Rad Laboratories 500-0007
Test tube 16×100 VWR 47729-576
Test tube 12×75 Ultident 170-14100005B
Cell incubator  Mandel Heracell 150
Low speed centrifuge IEC Centra8R
High speed centrifuge Beckman Avanti J8
High speed rotor for 250ml bottle Beckman JLA16.250
High speed rotor for 50ml tube Beckman JA30.50
Fow cytometry  BD Bio-sciences FACS Calibur
Spectrophotometer Beckman Series 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 Blades Becton Dickinson AcuteCare 371310 #10
Scalpel Handle Fine Science Tools Inc.  10003-12 #7
phase-contrast inverted microscope Olympus Optical CO., LTD.    CK2
high O2 gas mixture  VitalAire Canada Inc.
modular incubator chamber Billups-Rothenberg Inc. MIC-101
MaxQ 4000 incubated orbital shaker Barnstead Lab-Line,  SHKA4000-7
12-well tissue culture plate Becton Dickinson and Company 353043
Plastic tissue culture dishes (100 mm) Sarstedt, Inc. 83.1802
Surgical scissors Fine Science Tools Inc.  14060-09 Straight, sharp, 9cm longth
Half-curved Graefe forceps Fine Science Tools Inc.  11052-10
humidified CO2 incubator Mandel Scientific Company Inc.  SVH-51023421
 Histopathological examination 
formalin formaldehyde Sigma-Aldrich, Inc.  HT5011
paraffin Fisher scientific  International, Inc. T555
ethyl alcohol Merck KGaA, Darmstadt EX0278-1
 glutaraldehyde  Sigma-Aldrich, Inc.  G6403
Cacodylate Sigma-Aldrich, Inc.  31533
microscope slides VWR Scientific Inc.  48300-025 25x75mm
Xylene Fisher scientific  International, Inc. X5-4
Mayer's hematoxylin Sigma-Aldrich, Inc.  MHS16 Funnel with filter paper  
HCl  Fisher scientific  International, Inc.   A144s-500
eosin  Sigma-Aldrich, Inc.  HT110116 Funnel with filter paper  
Permount™ Mounting Medium Thermo Fisher Scientific Inc.  SP15-100
glass coverslip surgipath medical industries, Inc. 84503 24×24 #1 
TUNEL detection kit In Situ Cell Death Detection, POD 11 684 817 910
oven Despatch Industries Inc. LEB-1-20
rotary Microtome Leica Microsystems Inc. RM2145
filter paper Whatman International Ltd. 1003150 #3
Microscope Nikon Imaging Japan Inc. E800
staining dish complete Wheaton Industries, Inc. 900200 including dish, rack, cover
1.5 ml eppendorf tube Sarstedt Inc.  72.69 39x10mm
Orbital and Reciprocating Water Bath ExpotechUSA ORS200
phosphate buffered saline   GIBCO 14190-144
fume hood Nicram RD Service 3707E

Referências

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Yang, C., Xiong, W., Qiu, Q., Tahiri, H., Gagnon, C., Liu, G., Hardy, P. Generation of Lymphocytic Microparticles and Detection of their Proapoptotic Effect on Airway Epithelial Cells. J. Vis. Exp. (96), e52651, doi:10.3791/52651 (2015).

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