Method Article

Isolation, Characterization and Functional Examination of the Gingival Immune Cell Network

DOI:

10.3791/53736

⸱

February 16th, 2016

In This Article

Summary

Loading...
$$\rightleftharpoonup{xx}$$ $$\longleftharp{xx}$$, $$\longrightharp{xx}$$,

We have established a technique for the isolation, phenotypic characterization and functional analysis of immune cells from murine gingiva.

Abstract

Loading...
$$\rightleftharpoonup{xx}$$ $$\longleftharp{xx}$$, $$\longrightharp{xx}$$,

Immune cell networks in tissues play a vital role in mediating local immunity and maintaining tissue homeostasis, yet little is known of the resident immune cell populations in the oral mucosa and gingiva. We have established a technique for the isolation and study of immune cells from murine gingival tissues, an area of constant microbial exposure and a vulnerable site to a common inflammatory disease, periodontitis. Our protocol allows for a detailed phenotypic characterization of the immune cell populations resident in the gingiva, even at steady state. Our procedure also yields sufficient cells with high viability for use in functional studies, such as the assessment of cytokine secretion ex vivo. This combination of phenotypic and functional characterization of the gingival immune cell network should aid towards investigating the mechanisms involved in oral immunity and periodontal homeostasis, but will also advance our understanding of the mechanisms involved in local immunopathology.

Introduction

Loading...
$$\rightleftharpoonup{xx}$$ $$\longleftharp{xx}$$, $$\longrightharp{xx}$$,

Gingival tissues surround the human and murine dentition and are constantly exposed to the complex biofilm of the tooth 1. The immune cell network policing the gingival barrier is vital to maintaining tissue integrity, ensuring homeostasis with the local commensal microbes and, at the same time, providing effective immunity against pathogenic challenge 2. To achieve homeostasis, the immune system is carefully tailored to the gingival environment creating a highly-specialized immune cell network, yet little detail is known of the gingival immune cell populations and their role in maintaining tissue immunity 2.

Access restricted. Please log in or start a trial to view this content.

Protocol

Loading...
$$\rightleftharpoonup{xx}$$ $$\longleftharp{xx}$$, $$\longrightharp{xx}$$,

All experimental procedures described in this protocol followed required guidelines and were approved by the Institutional Animal Care and Use Committee, NIDCR/NIH.

1. Prepare in Advance

  1. Prepare Complete media: RPMI supplemented with 2 mM L-glutamine, 100 units/ml penicillin, 100 ug/ml streptomycin and 10% FBS.
  2. Prepare DNase media: 50 ml of RPMI media supplemented with 7.5 µg DNase (Make fresh, keep on ice at all times).
  3. Prepare Collagenase-DNase media: 5 ml of DNase media plus 3.2 mg/ml of Collagenase Type IV (Make fresh, keep on ice at all times).
  4. Pre-cool FACS buffer: 0.5 % FBS diluted in PBS.
  5. Pre-cool....

Access restricted. Please log in or start a trial to view this content.

Results

Loading...
$$\rightleftharpoonup{xx}$$ $$\longleftharp{xx}$$, $$\longrightharp{xx}$$,

To illustrate application of the protocol, we show representative results examining the immune cell network in the gingiva of mice with and without periodontitis (WT vs. LFA-/-, Figure 2A-C). Representative FACS plots show live CD45+ hematopoietic cells in the gingiva (Figure 2A, 2C). Isolation and processing of immune cells with this protocol yields sufficient cells to perform ex vivo stimu.......

Access restricted. Please log in or start a trial to view this content.

Discussion

Loading...
$$\rightleftharpoonup{xx}$$ $$\longleftharp{xx}$$, $$\longrightharp{xx}$$,

The current technique successfully yields a large number of immune cells (from a single mouse) suitable, not only for phenotypic characterization, but also for functional studies ex vivo. Another group had previously published a protocol to isolate and characterize murine gingival immune cells and introduced the value of using multicolor flow cytometry in the study of periodontitis in animal models 9. Following considerable troubleshooting the key modification in this protocol was to include dissectio.......

Access restricted. Please log in or start a trial to view this content.

Disclosures

Loading...
$$\rightleftharpoonup{xx}$$ $$\longleftharp{xx}$$, $$\longrightharp{xx}$$,

Authors have nothing to disclose

Acknowledgements

Loading...
$$\rightleftharpoonup{xx}$$ $$\longleftharp{xx}$$, $$\longrightharp{xx}$$,

Authors were funded in part by the intramural program of NIDCR (N.M.M) and supported by a Wellcome Trust Stepping Stones Fellowship (097820/Z/11/B to J.E.K) and by a Manchester Collaborative Centre for Inflammation Research grant (to J.E.K). The authors thank Teresa Wild for critically reviewing the manuscript.

....

Access restricted. Please log in or start a trial to view this content.

Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Fine ScissorsFine science tools14058-11
Scalpel Handle #3Fine science tools10003-12
Scalpel Blades #10Fine science tools10010-00Sterile
Splinter ForcepsIntegra Miltex6-304
Needles with regular bevel BD Medical30510927 G, 12.7 mm length
Monoject syringesCovidien8881513934Luer-lock tip, 3 ml
PBS, pH 7.4Life Technologies10010-049Without Calcium and Magnesium
RPMI 1640Lonza12-167FWithout L-glutamine
DNase I from bovine pancreasSigma-AldrichDN25-1G
Collagenase type IVGibco (by Life technologies)17104-019
Fetal Bovine SerumGemini Bio-products100-106
Gentamicin 50 mg/mlQuality biological120-098-661EA
Pen StrepGibco (by Life technologies)15140-122
L-GlutamineGibco (by Life technologies)25030-081
0.5 M EDTA pH 8.0Quality biological351-027-721EA
50 ml tubesCorning352070Polypropylene, sterile
70 μM Cell StrainersCorning352350
Petri dishesCorning351029Sterile
5 ml FACS tubesCorning352052Sterile
BD GolgiPlugBD Biosciences555029Contains brefeldin A solution
Phorbol 12-Myristate 13-Acetate (PMA)Sigma-AldrichP8139
Ionomycin Calcium SaltSigma-Aldrich13909
Saponin from quillaja barkSigma-AldrichS4521
LIVE/DEAD Fixable Aqua Dead Cell Stain KitLife TechnologiesL34957
Anti-Mouse CD45 Alexa Fluor 700eBioscience56-0451-82
Anti-Mouse CD4 eFluor 450eBioscience48-0042-82
Anti-Mouse TCR beta APC eFluor 780eBioscience47-5961-82
Anti-Mouse gamma delta TCR FITCeBioscience11-5711-82
Anti-Mouse IL-17A APCeBioscience12-7311-82
Anti-Mouse IFN-γ PEeBioscience11-5931-82
Anti-Mouse NK1.1 PE-Cy7eBioscience25-5941-82
Anti-Mouse CD90.2 APC eFluor 780eBioscience47-0902-82
Anti-Mouse CD3e FITCeBioscience11-0031-82
Anti-Mouse CD19 FITCeBioscience11-0193-82
Anti-Mouse CD11b FITCeBioscience11-0112-82
Anti-Mouse CD11c FITCeBioscience11-0114-82
Anti-Mouse TCR beta FITCeBioscience11-5961-82
Anti-Mouse Ly-6G FITCeBioscience11-5931-82
Anti-Mouse Ly-6C FITCBD Pharmingen553104

References

Loading...
$$\rightleftharpoonup{xx}$$ $$\longleftharp{xx}$$, $$\longrightharp{xx}$$,
  1. Aas, J. A., Paster, B. J., Stokes, L. N., Olsen, I., Dewhirst, F. E. Defining The Normal Bacterial Flora Of The Oral Cavity. J Clin Microbiol. 43, 5721-5732 (2005).
  2. Belkaid, Y., Naik, S. Compartmentalized And Systemic Control Of Tissue Immunity By Commensals. Nat Immunol.

Access restricted. Please log in or start a trial to view this content.

Reprints and Permissions

Request permission to reuse the text or figures of this JoVE article

Request Permission

Tags

Gingival Immune CellsImmune Cell IsolationTissue DigestionFlow CytometryCytokine SecretionCollagenase DNaseCell StrainerEx Vivo StimulationPhenotypic CharacterizationFunctional Examination

Related Articles