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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Results
  • Discussion
  • Disclosures
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

We describe a protocol to efficiently isolate skin resident T cells from human skin biopsies. This protocol yields sufficient numbers of viable human skin resident lymphocytes for flow cytometric analysis and ex vivo culture.

Abstract

Human skin has an important barrier function and contains various immune cells that contribute to tissue homeostasis and protection from pathogens. As the skin is relatively easy to access, it provides an ideal platform to study peripheral immune regulatory mechanisms. Immune resident cells in healthy skin conduct immunosurveillance, but also play an important role in the development of inflammatory skin disorders, such as psoriasis. Despite emerging insights, our understanding of the biology underlying various inflammatory skin diseases is still limited. There is a need for good quality (single) cell populations isolated from biopsied skin samples. So far, isolation procedures have been seriously hampered by a lack of obtaining a sufficient number of viable cells. Isolation and subsequent analysis have also been affected by the loss of immune cell lineage markers, due to the mechanical and chemical stress caused by the current dissociation procedures to obtain single cell suspension. Here, we describe a modified method to isolate T cells from both healthy and involved psoriatic human skin by combining mechanical skin dissociation using an automated tissue dissociator and collagenase treatment. This methodology preserves expression of most immune lineage markers such as CD4, CD8, Foxp3 and CD11c upon the preparation of single cell suspensions. Examples of successful CD4+ T cell isolation and subsequent phenotypic and functional analysis are shown.

Introduction

The skin, as the primary interface between the body and the environment, provides the first line of defence against external physical, chemical and biological insults such as wounding, ultraviolet radiation and micro-organisms. Skin comprises two main compartments, the epidermis and the dermis, and contains a variety of immune cells including Langerhans cells, macrophages, dendritic cells (DCs), and about 20 billion memory T cells, nearly twice the number present in the entire blood volume1,2. A growing body of data supports the notion that the skin has essential immunological functions, both during tissue homeostasis and in various pathological conditions.....

Protocol

NOTE: Skin biopsies from healthy individuals were obtained from abdominal skin leftover of individuals undergoing elective plastic surgery after oral or written informed consent for scientific use. The use of human skin was approved and in accordance with the regulations set by the Medical Ethical Committees for human research of the Radboud university medical centre, Nijmegen, the Netherlands and University of Essen, Germany.

1. Preparation of Single Cell Suspensions from Human Skin (Work Sterile in a Flow-cabinet if Subsequent Cell Culture is Required)

  1. Prepare cell culture medium: RPMI 1640 + penicillin/streptomycin (final con....

Results

The protocol presented here will yield between 2,200 ± 615 (mean ± SEM, skin of healthy volunteers) up to 178,000 ± 760 (mean ± SEM, lesional skin of psoriasis patients) viable lymphocytes from human skin when using a single 4 mm skin biopsy.

Different types of CD45+ cells were identified in single-cell suspensions derived from skin of healthy individuals including CD4+ T-cells (~45%), CD8+ T-cells (~30%), and CD11c+ DCs (~5%), wh.......

Discussion

Here, we present a protocol to efficiently isolate skin resident T cells from human skin biopsies. The advantage of this protocol is the isolation of relatively high numbers of viable lymphocytes, and expressing relevant surface markers. The cell subsets identified were: CD11c+ DCs, CD4+ and CD8+ T cells and Foxp3+CD25+ cells. Importantly, ex vivo culture of isolated skin resident T cells was very well feasible and allowed for subsequent functional analysis........

Disclosures

The authors have nothing to disclose.

Acknowledgements

Skin biopsies from psoriasis patients were kindly provided by Dr. Andreas Koerber (Dermatology department at University of Essen, Germany) after oral or written informed consent for scientific use. 

X.H. is also supported by NSFC 61263039 and NSFC 11101321.

....

Materials

NameCompanyCatalog NumberComments
Name of Reagent/ EquipmentCompanyCatalog NumberComments/Description
Disposable Biopsy PunchKai EuropeBP-40F4 mm
Disposable sterile scalpelsDalhausen1100000510
gentleMACS C tubeMiltenyi Biotech130-093-237Blue-capped, used as the dissociation tube.
gentleMACS DissociatorMiltenyi Biotech130-093-235Automated tissue dissociator. Using the "program spleen_01" for dissociation of the skin biopsy.
Cell strainer BD35235070 µm nylon
96-well U-bottom plateGreiner Bio-One650180
RPMI 1640Life Technologies22409-015
Sodium pyruvateLife Technologies11360-039
GlutaMAXLife Technologies35050-061
Penicillin/StreptomycinLife Technologies15140-122
Human Pooled Serum (HPS)in house prepared
Collagenase ISigma-AldrichC2674Type 1-A, suitable for cell culture
DNase ICalbiochem260913
PBSB Braun3623140
BSASigma-AldrichA4503-500G
Fixable Viability Dye (FVD) APC-eFluo780eBioscience65-0865-18Stain dead cells prior to cell fixation; dilute with PBS at 1:1000
Fixation/Permeabilization ConcentrateeBioscience00-5123-43
Fixation/Permeabilization DiluenteBioscience00-5223-56
Permeabilization Buffer (10x)eBioscience00-8333-56
BV421 Mouse anti-human CD45BD563879Clone: HI30; dilution factor 1:50
FITC Mouse anti-human CD14DakoT0844Clone: TUK4; dilution factor 1:50
PE Mouse anti-human CD56DakoR7127Clone: MOC-1; dilution factor 1:50
ECD Mouse anti-human CD3Beckman - CoulterA07748Clone: UCHT1; dilution factor 1:50 for surface staining; dilution factor 1:25 for intracellular staining.
PC5.5 Mouse anti-human CD4Beckman - CoulterB16491Clone: 13B8.2; dilution factor 1:200
PeCy7 Mouse anti-human CD11cBeckman - CoulterA80249Clone: BU15; dilution factor 1:50
APC Mouse anti-human CD1cMiltenyi Biotech130-090-903Clone: AD5-8E7; dilution factor 1:10
APC-AlexFluo700 Mouse anti-human CD8Beckman - CoulterA66332Clone: B9.11; dilution factor 1:400
APC-AlexFluo750 Mouse anti-human CD19Beckman - CoulterA94681Clone: J3-119; dilution factor 1:50
PeCy7 Mouse anti-human CD25eBioscienceAD5-8E7Clone: BC96; dilution factor 1:50
 PE Rat anti-human CLAMiltenyi Biotech130-091-635clone: HECA-452; dilution factor 1:
eFluo450 Rat anti-human Foxp3eBIoscience48-4776-42Clone: PCH101; intracellular staining; dilution factor 1:50
AlexFluo488 Mouse anti-human IL-17AeBioscience53-7179-42Clone: eBio64DEC17; intracellular staining; dilution factor 1:50
PeCy7 Mouse anti-human IFNgeBioscience25-7319-41Clone: 4S.B3; intracellular staining; dilution factor 1:400
Flow-Count FluorospheresBeckman - Coulter7547053Counting beads, for flow cytometry

References

  1. Clark, R. A., et al. The vast majority of CLA+ T cells are resident in normal skin. J Immunol. 176, 4431-4439 (2006).
  2. Zaba, L. C., Fuentes-Duculan, J., Steinman, R. M., Krueger, J. G., Lowes, M. A.

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