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In This Article

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

Summary

The here introduced protocol allows characterization of the lung homing capacity of primary human lymphocytes under in vivo inflammatory conditions. Pulmonary infiltration of adoptively transferred human immune cells in a mouse model of allergic inflammation can be imaged and quantified by light-sheet fluorescence microscopy of chemically cleared lung tissue.

Abstract

Overwhelming tissue accumulation of highly activated immune cells represents a hallmark of various chronic inflammatory diseases and emerged as an attractive therapeutic target in the clinical management of affected patients. In order to further optimize strategies aiming at therapeutic regulation of pathologically imbalanced tissue infiltration of pro-inflammatory immune cells, it will be of particular importance to achieve improved insights into disease- and organ-specific homing properties of peripheral lymphocytes. The here described experimental protocol allows to monitor lung accumulation of fluorescently labeled and adoptively transferred human lymphocytes in the context of papain-induced pulmonary inflammation. In contrast to standard in vitro assays frequently used for the analysis of immune cell migration and chemotaxis, the now introduced in vivo setting takes into account lung-specific aspects of tissue organization and the influence of the complex inflammatory scenario taking place in the living murine organism. Moreover, three-dimensional cross-sectional light-sheet fluorescence microscopic imaging does not only provide quantitative data on infiltrating immune cells, but also depicts the pattern of immune cell localization within the inflamed lung. Overall, we are able to introduce an innovative technique of high value for immunological research in the field of chronic inflammatory lung diseases, which can be easily applied by following the provided step-by-step protocol.

Introduction

Classic inflammatory disorders of the lung, such as allergic asthma and chronic obstructive pulmonary disease (COPD), are well known to be driven by an increased recruitment of activated lymphocytes into the pulmonary tissue1,2. Lymphocyte-released cytokines (e.g., IL-4, IL-5, IL-9, IL-13, IFN-γ and TNF-α) further promote chemotaxis of innate and adaptive immune cells, induce fibrotic airway remodeling or directly damage the lung parenchyma2. So far, the underlying mechanisms responsible for the pathological accumulation of lymphocytes within lung tissue are not yet fully unde....

Protocol

Experiments involving animals were performed in accordance with protocols approved by the relevant local authorities in Erlangen (Regierung von Unterfranken, Würzburg, Germany). Mice were housed under specific pathogen-free conditions. The collection of human blood was approved by the local ethical committee and the institutional review board of the University of Erlangen-Nuremberg. Each patient gave written informed consent.

1. Induce Allergic Lung Inflammation in Mice

Representative Results

The presented protocol describes an experimental mouse model, which allows monitoring and quantifying the accumulation of adoptively transferred human T lymphocytes in the lung via light-sheet fluorescence microscopy. Figure 1A provides a schematic overview of the in vivo steps of the experimental schedule. In order to guarantee reliable results, it is of substantial importance to ensure a good quality of the isolated and fluorescently labeled human CD4+ T ce.......

Discussion

The here described experimental setting provides the opportunity to monitor the lung homing capacity of primary human immune cells under in vivo inflammatory conditions and thereby relevantly complements classically performed in vitro adhesion and chemotaxis assays. To take into account specific anatomic organ characteristics of the lung, important aspects of immune cell homing (including chemotaxis and cell distribution within the target organ) as well as the clinical relevance and transfera.......

Acknowledgements

The authors gratefully acknowledge funding by the DFG Collaborative Research Centers SFB 1181 and TRR 241. The Optical Imaging Centre Erlangen (OICE) and in particular Ralf Palmisano, Philipp Tripal and Tina Fraaß (Project Z2 of the DFG CRC 1181) are acknowledged for expert technical support for light-sheet fluorescence microscopic imaging.

....

Materials

NameCompanyCatalog NumberComments
Agarose NEEO UltraCarl Roth GmbH + Co. KG, Karlsruhe, Germany2267.4
AlexaFlour594 anti-human CD45 antibodyBioLegend, San Diego, USA304060
Ammonium chlorideCarl Roth GmbH + Co. KG, Karlsruhe, GermanyK2981
Cannula 21 GBecton, Dickinson and Company, Franklin Lakes, USA301300
Cell proliferation dye eflour670eBioscience Inc., San Diego, USA65-0840-85
CD4 MicroBeads, humanMiltenyi Biotech GmbH, Bergisch-Gladbach, Germany130-045-101
EDTA (ethylenediaminetetraacetic acid)Carl Roth GmbH + Co. KG, Karlsruhe, Germany8043.1
Potassium-EDTA blood collection tube, 9 mlSarstedt AG & Co., Nümbrecht, Germany21066001
Ethly cinnamate (ECi)Sigma-Aldrich, Steinheim, Germany112372-100G
Ethanol ≥ 99.5 % (EtOH)Carl Roth GmbH + Co. KG, Karlsruhe, Germany5054.3
FBS (fetal bovine serum) Good FortePAN-Biotech GmbH, Aidenbach, GermanyP40-47500
Filter 100 µm VWR International Germany GmbH, Darmstadt, Germany732-2758
Imaris Image Analysis Software 9.0.2Bitplane AG, Zurich, Switzerlandn.a.
ImspectorPro softwareAbberior Instruments GmbH, Göttingen, Germanyn.a.
Ketamin Inresa Arzneimittel GmbH, Freiburg, Germany3617KET-V
LaVision UltraMicroscope IILaVision BioTec GmbH, Bielefeld, Germanyn.a.
MACS MultiStandMiltenyi Biotech GmbH, Bergisch-Gladbach, Germany130-042-303
Multifly cannula 20 GSarstedt AG & Co., Nümbrecht, Germany851638035
30 G needleB. Braun Melsungen AG, Melsungen, Hessen, Germany9161502
Neubauer counting chamberneoLab Migge GmbH, Heidelberg, GermanyC-1003
Pattex GlueHenkel AG & Co, Düsseldorf, GermanyPSK1C
LS columnMiltenyi Biotech GmbH, Bergisch-Gladbach, Germany130-042-401
Lymphocyte Separation Media (Density 1,077 g/ml)anprotecAC-AF-0018
RPMI medium (Gibco) Life Technologies GmbH,
Darmstadt, Germany61870-010
PapainMerck1,071,440,025
PBS Dulbecco (phosphate buffered saline)Biochrom GmbH, Berlin, GermanyL182-10
PerCP/Cy5.5 anti-human CD4BioLegend, San Diego, USA317428
PerCP/Cy5.5 mouse IgG2b, κ isotype CtrlBioLegend, San Diego, USA400337
PFA (paraformaldehyde)Carl Roth GmbH + Co. KG, Karlsruhe, Germany0335.1
Potassium hydrogen carbonateCarl Roth GmbH + Co. KG, Karlsruhe, GermanyP7481
Serological pipette 10 mlSarstedt AG & Co., Nümbrecht, Germany86.1254.001 
Syringe 1 mlB. Braun Melsungen AG, Melsungen, Hessen, Germany9166017V
Syringe 5 mlBecton, Dickinson and Company, Franklin Lakes, USA260067
Syringe 20 mlBecton, Dickinson and Company, Franklin Lakes, USA260069
Tube 1.5 mlSarstedt AG & Co., Nümbrecht, Germany72,706,400
Tube 2 mlSarstedt AG & Co., Nümbrecht, Germany72.695.400 
Tube 2 ml, brownSarstedt AG & Co., Nümbrecht, Germany72,695,001
Tube 15 mlSarstedt AG & Co., Nümbrecht, Germany62.554.502 
Tube 50 mlSarstedt AG & Co., Nümbrecht, Germany62.547.254 
QuadroMACS SeparatorMiltenyi Biotech GmbH, Bergisch-Gladbach, Germany130-090-976
Xylazin (Rompun 2%)Bayer Vital GmbH, Leverkusen, GermanyKPOBD32

References

  1. Medoff, B. D., Thomas, S. Y., Luster, A. D. T cell trafficking in allergic asthma: the ins and outs. Annual Review of Immunology. 26, 205-232 (2008).
  2. Baraldo, S., Lokar Oliani, K., Turato, G., Zuin, R., Saetta, M. The Role of Lymphocy....

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