Summary

İzolasyon ve murin lenfositlerin aktivasyonu

Published: October 30, 2016
doi:

Summary

Lymphocytes are the major players in adaptive immune responses. Here, we present a lymphocyte purification protocol to determine the physiological functions of the desired molecules in lymphocyte activation in vitro and in vivo. The described experimental procedures are suitable for comparing functional capacities between control and genetically modified lymphocytes.

Abstract

B and T cells, with their extremely diverse antigen-receptor repertoires, have the ability to mount specific immune responses against almost any invading pathogen1,2. Understandably, such intricate abilities are controlled by a large number of molecules involved in various cellular processes to ensure timely and spatially regulated immune responses3. Here, we describe experimental procedures that allow rapid isolation of highly purified murine lymphocytes using magnetic cell sorting technology. The resulting purified lymphocytes can then be subjected to various in vitro or in vivo functional assays, such as the determination of lymphocyte signaling capacity upon stimulation by immunoblotting4 and the investigation of proliferative abilities by 3H-thymidine incorporation or carboxyfluorescein diacetate succinimidyl ester (CFSE) labeling5-7. In addition to comparing the functional capacities of control and genetically modified lymphocytes, we can also determine the T cell stimulatory capacity of antigen-presenting cells (APCs) in vivo, as shown in our representative results using transplanted CFSE-labeled OT-I T cells.

Introduction

Mature lymphocytes generally exist in the resting state if there is no pre-existing infection or inflammation in the individual. Therefore, it is important to retain the naïve status of lymphocytes during the isolation process before performing in vitro or in vivo functional assays. The key to ensuring consistent and reproducible results is to limit any unnecessary manipulation of the cells.

Magnetic cell sorting utilizes antibodies and microbeads to label cells so as to enrich the cell population of interest. With this approach, there are two purification strategies: positive enrichment and negative depletion. Positive enrichment enriches the cell population of interest using an antibody that binds to the target cells. Negative depletion, on the other hand, depletes non-target cells, leaving the cell population of interest. In our lab, we prefer negative depletion to positive enrichment because the binding of antibodies to the target cells could potentially alter cell features and behavior. In fact, many established cell surface markers suitable for the isolation of a particular cell population are also functional receptors.

Magnetic cell sorting not only yields highly pure populations of viable target cells, it is also less time-consuming and avoids the cellular stress induced by high-pressure flow used in fluorescence-activated cell sorting (FACS). By labeling the unwanted cell populations and depleting them using a magnetic separation column, we are able to perform rapid cell isolation without compromising the viability of the target cell population. In this protocol, we demonstrate the use of negative depletion strategies to purify naïve B cells or T cells.

Protocol

Tüm fareler yetiştirilen ve özel patojen içermeyen koşullar altında korunur ve tüm fare protokolleri Kurumsal Hayvan Bakım ve Kullanım Komitesi kurallarına uygun olarak yürütülmektedir vardır. Tamponlar ve Reaktiflerin hazırlanması 1. 55 uM 2-merkaptoetanol tamamlandı Roswell Park Memorial Institute (RPMI) ortamında (% 10 ısı ile inaktive edilmiş fetal büyükbaş hayvan serumu (FBS), 2 mM L-glutamin, penisilin (100 lU / ml) / streptomisin (100 ug / ml) hazır…

Representative Results

lenfositlerin manyetik hücre saflaştırma kullanıcılara zaman nispeten kısa bir miktarda bir hedef hücre popülasyonu arındırmak için izin verir. Bizim tükenmesi protokolü kullanarak, arıtıldıktan sonra 94.2% (için 72,8% (önceki arıtma) den (rekombinasyon aktive gen 1 (RAG-1) -açıklı farelerde OT-I) CD8 T hücrelerinin yüzdesini artırmak başardık; Şekil 1A) 4,5. Bu arıtılmış, lenfositler, daha sonra olan limfosit proliferasyon ve s…

Discussion

Bu protokol, lenfoid organların lenfositlerin saflaştırılması için bir prosedürü göstermektedir. manyetik boncuk sıralama kullanılarak hücre arıtma canlı, yüksek düzeyde saflaştırılmış hedef hücreleri verimleri hızlı ve basit bir yöntemdir.

Protokol çerçevesinde kritik adımlar

Hücre canlılığı, ve hücre verimi

In vitro olarak hematopoietik kökenli hücrelerin canlılığını m…

Disclosures

The authors have nothing to disclose.

Acknowledgements

Çalışma Eğitim, Singapur Bakanlığı (AcRF Tier1-RG40 / 13 ve Tier2-MOE2013-T2-2-038) tarafından desteklenmektedir. el yazması Obrizus Communications Amy Sullivan tarafından düzenlendi.

Materials

Materials
RPMI 1640 (without L-Glutamine) Gibco 31870025
Fetal Bovine Serum Heat inactivated 
L-glutamine Gibco 25030024
Penicillin/Streptomycin Gibco 15140114
2-mercaptoethanol Gibco 21985023
Anti-CD43 magnetic microbeads Miltenyi Biotec 130-049-801 Mix well prior use
Streptavidin microbeads Miltenyi Biotec 130-048-101 Mix well prior use
Anti-Annexin V magnetic beads Miltenyi Biotec 130-090-201 Mix well prior use
MACS LD  Miltenyi Biotec 130-042-901
96-well U-bottom sterile culture plate Greiner Bio-one 650180
96-well F-bottom sterile culture plate Greiner Bio-one 655180
100 μm cell strainer mesh To sterilize using UV radiation prior use
0.2 μm  sterile disposable filter units Nalgene 567-0020 Can be substituted with any sterile filter device
CellTrace Violet Invitrogen C34557 CTV for short; alternative to CFSE
CellTrace Yellow Invitrogen C34567 CTY for short; alternative to CFSE
CellTrace Far Red Invitrogen C34564 CTFR for short; alternative to CFSE
Cell Proliferation Dye eFluor 670 eBioscience 65-0840 CPD670 for short; alternative to CFSE
PKH26 Sigma Aldrich PKH26GL PKH26, alternative to CFSE
Name Company Catalog Number Comments
Chemicals
Dextrose Sigma Aldrich G7021
Potassium phosphate monobasic Sigma Aldrich P5655
Sodium phosphate dibasic Sigma Aldrich S5136
Phenol Red Sigma Aldrich P0290
Calcium chloride dihydrate Sigma Aldrich C7902
Potassium chloride Sigma Aldrich P5405
Sodium chloride Merck Millipore S7653 Can use from other sources
Magnesium chloride hexahydrate Sigma Aldrich M2393
Magnesium sulfate Sigma Aldrich M2643
Ammonium chloride Sigma Aldrich A9434
Tris-base
Dimethyl Sulfoxide Sigma Aldrich  D8418
(5-(and 6-) carboxyfluorescein diacetate succinimidyl ester (CFSE) Molecular Probes C-1157 Reconstitute in DMSO
Phorbol 12,13-dibutyrate (PBDU, Phorbol ester) Sigma Aldrich P1269
A23187 (Calcium ionophore) Sigma Aldrich C7522
Name Company Catalog Number Comments
Antibodies and recombinant protein
CD11b biotin (clone m1/70) Biolegend 101204 T cell depletion cocktail
CD11c biotin (clone N418) Biolegend 117304 T cell depletion cocktail
Gr-1 biotin (clone RB6-8C5) Biolegend 108404 T cell depletion cocktail
Ter119 biotin (clone Ter119) Biolegend 116204 T cell depletion cocktail
TCR-γδ biotin (clone GL-3) Biolegend 118103 T cell depletion cocktail
CD19 biotin (clone 6D5) Biolegend 115504 T cell depletion cocktail
B220 biotin (clone RA3-6B2) Biolegend 103204 T cell depletion cocktail
CD49b biotin (clone DX5) Biolegend 108904 T cell depletion cocktail
CD4 biotin (clone GK1.5) Biolegend 100404 T cell depletion cocktail
CD8 biotin (clone 53-6.7) Biolegend 100704 T cell depletion cocktail
F(ab’)2 goat anti-mouse IgM (plate coated) Jackson ImmunoResearch  115-006-075 50 µl/well for coating (96-well)
Anti-mouse CD40 mAb (plate coated) Pharmingen  553722 50 µl/well for coating (96-well)
Recombinant IL-4 ProSpec  Cyt-282
LPS from E. coli Serotype 055:B5 Sigma Aldrich L-4005
Anti-CD3 (clone clone OKT3) (plate coated) eBioscience  16-0037-85 50 µl/well for coating (96-well)
Anti-CD28 (clone clone 37.51 ) (plate coated)  eBioscience  16-0281-85 50 µl/well for coating (96-well)
Recombinant IL-2 ProSpec Cyt-370
Albumin from chicken egg white, Ovalbumin Sigma Aldrich A7641

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Cite This Article
Lim, J. F., Berger, H., Su, I. Isolation and Activation of Murine Lymphocytes. J. Vis. Exp. (116), e54596, doi:10.3791/54596 (2016).

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