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Method Article

Fluorescence-activated Cell Sorting for Purification of Plasmacytoid Dendritic Cells from the Mouse Bone Marrow

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DOI:

10.3791/54641

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November 4th, 2016

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In This Article

Summary

We report a protocol using fluorescence-activated cell sorting to isolate plasmacytoid dendritic cells (pDC) with high purity from the bone marrow of lupus-prone mice for functional studies of pDC.

Abstract

Fluorescence-activated cell sorting (FACS) is a technique to purify specific cell populations based on phenotypes detected by flow cytometry. This method enables researchers to better understand the characteristics of a single cell population without the influence of other cells. Compared to other methods of cell enrichment, such as magnetic-activated cell sorting (MCS), FACS is more flexible and accurate for cell separation due to the ability of phenotype detection by flow cytometry. In addition, FACS is usually capable of separating multiple cell populations simultaneously, which improves the efficiency and diversity of experiments. Although FACS has some limitations, it has been broadly used to purify cells for functional studies in both in vitro and in vivo settings. Here we report a protocol using fluorescence-activated cell sorting to isolate a very rare population of immune cells, plasmacytoid dendritic cells (pDC), with high purity from the bone marrow of lupus-prone mice for in vitro functional studies of pDC.

Introduction

Efficient separation of a cell population of choice from other cells enables studies of the population that may not be possible otherwise. Fluorescence-activated cell sorting (FACS) is a method to enrich an interesting cell population with high purity. 1,2 Different cell types usually express unique molecules, or a unique combination of several molecules, on the plasma membrane that can distinguish one cell population from another. Upon binding of these cell surface molecules by specific fluorescence-conjugated antibodies, a detecting machine called flow cytometer/sorter is able to excite and detect the light signals of different fluorescent dyes that repre....

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Protocol

NOTE: MRL/Mp-Faslpr (MRL/lpr) lupus-prone mice were bred and maintained in a specific pathogen-free facility following the requirements of Institutional Animal Care and Use Committee (IACUC) at Virginia Tech (Animal Welfare Assurance Number: A3208-01). This study was carried out in strict accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. All animal experiments were conducted under IACUC protocol #12-062.

1. Cell Culture Medium and Sorting Buffer

  1. Prepare complete cell culture medium (C10) using RPMI 1640 supplemented with 10% fetal bovine serum, 1 mM sodium pyr....

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Results

We aimed to enrich bone marrow pDC with high purity, and without the influence of other cell types, from MRL/lpr lupus-prone mice of both young and old age to study the functional changes of pDC regarding their ability to produce IFNα. The first purification strategy used was MCS, which, as Figure 1 shows, led to only 7.75% purity after the enrichment. Compared to MCS, FACS enriched pDC with purity as high as 96.4%. To ensure high purity, a step-by-step gating strategy wa.......

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Discussion

The protocol described in this manuscript is for high purity enrichment of live pDC that retain the ability to produce IFNα. The applications of this protocol include, but are not limited to, purification of pDC and/or any other mononuclear cells from the bone marrow of MRL/lpr and any other mouse strains for studies of cellular and molecular functions. Several critical steps in this protocol are to ensure high viability and purity of the sorted pDC. The first key step is the release of bone marrow from bones. To mi.......

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Disclosures

The authors declare that there is no conflict of interest regarding the publication of this paper.

Acknowledgements

We thank Flow Cytometry Laboratory at Virginia-Maryland College of Veterinary Medicine for the use of flow cytometry core facility. This work was supported by XML's startup funds. XL is a Stamps Fellow in the Biomedical and Veterinary Sciences graduate program.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
RPMI 1640gibco by life technologies11875-093
Fetal bovine serumHyCloneSH30396.03
Sodium pyruvategibco by life technologies11360-070
MEM non-essential amino acidsgibco by life technologies11140-050
HEPESgibco by life technologies15630-080
2-mercaptoethanolgibco by life technologies21985-023
L-glutamine gibco by life technologies25030-164
Penicillin-Streptomycingibco by life technologies15140-122
1x Hank’s Balanced Salt Solution gibco by life technologies14175-079
MACS BSA Stock SolutionMiltenyi Biotec130-091-376
MgCl2SIGMAM8266
DNase ISIGMAD4527
Red blood cell (RBC) lysis buffer eBioscience00-4300-54
Density gradient mediumGE Healthcare17-1440-02Ficoll-Paque Plus 
anti-mouse CD19-PEBD Pharmingen553786
anti-mouse CD11c-PEeBioscience12-0114-82
anti-mouse CD11b-APC-CY7BD Pharmingen557657
anti-mouse PDCA-1-FITCeBioscience11-3172-81
anti-mouse B220-V500 BD Pharmingen561226
DAPIinvitrogenD3571
Plasmacytoid Dendritic Cell Isolation Kit II, mouseMiltenyi Biotec130-092-786
BD FACSAria I flow cytometer BD Biosciences643178
BD FACS Diva version 6BD Biosciences

References

  1. Bonner, W. A., Hulett, H. R., Sweet, R. G., Herzenberg, L. A. Fluorescence activated cell sorting. Rev Sci Instrum. 43 (3), 404-409 (1972).
  2. Herzenberg, L. A., et al. The history and future of the fluorescence activated cell sorter and flow cytometry: a view from Sta....

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