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Method Article

Flow Cytometry Protocols for Surface and Intracellular Antigen Analyses of Neural Cell Types

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DOI:

10.3791/52241

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December 18th, 2014

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In This Article

Summary

We provide a detailed description of a protocol for flow cytometric analysis of surface antigens and/or intracellular antigens in neural cell types. Critical aspects of experimental planning, step-by-step methodological procedures, and fundamental principles of flow cytometry are explained in order to enable neurobiologists to exploit this powerful technology.

Abstract

Flow cytometry has been extensively used to define cell populations in immunology, hematology and oncology. Here, we provide a detailed description of protocols for flow cytometric analysis of the cluster of differentiation (CD) surface antigens and intracellular antigens in neural cell types. Our step-by-step description of the methodological procedures include: the harvesting of neural in vitro cultures, an optional carboxyfluorescein succinimidyl ester (CFSE)-labeling step, followed by surface antigen staining with conjugated CD antibodies (e.g., CD24, CD54), and subsequent intracellar antigen detection via primary/secondary antibodies or fluorescently labeled Fab fragments (Zenon labeling). The video demonstrates the most critical steps. Moreover, principles of experimental planning, the inclusion of critical controls, and fundamentals of flow cytometric analysis (identification of target population and exclusion of debris; gating strategy; compensation for spectral overlap) are briefly explained in order to enable neurobiologists with limited prior knowledge or specific training in flow cytometry to assess its utility and to better exploit this powerful methodology.

Introduction

Flow cytometry has been extensively exploited in immunology, hematology and oncology to define cell populations via intrinsic scatter properties, cell surface antigen expression, and other fluorescence parameters1-3. Our insights into blood lineage development and disease are a result to a significant degree of the continuous refinement of this methodology after its initial implementation4,5. Increased awareness of the quantitative and overall analytic potential of flow cytometry has recently encouraged its more widespread use in stem cell research and may enable similarly profound progress in a shorter time frame6. However, the applic....

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Protocol

1. Neural Cell Harvesting

  1. Assessment by microscope:
    1. Prior to initiating an experiment, check the status of the culture with bright-field or phase contrast microscopy.
      NOTE: While primary neural tissue obtained from dissections is, in principle, equally amenable to flow cytometric analysis14,28, please note that the protocol’s focus is on cells obtained from in vitro neural cell systems.
  2. Harvesting cells7:
    1. Gently wash the dish/flask of adherent cells with Mg2+/ Ca2+ free phosphate-buffered saline (PBS) at RT (e.g., 5 ml for T75 flask, 3 ml per....

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Results

The protocol presented here allows for versatile experimental approaches (Figure 2). In its shortest version (steps 1, 3 and 6), it can be considered a guide for simple staining of surface antigens.  In its more complex form, a number of co-labeling paradigms with a range of intracellular antigens can be pursued (optional steps 2 and/or 4 to 5). Moreover, the CFSE-labeling step exemplifies its utility for cell label.......

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Discussion

The protocol presented here is well established for neural cell cultures derived from human stem cells, but can be equally applied to other neural cell sources including primary tissue or neural cell lines. In addition to embryonic sources, neural stem or progenitor cells can be extracted from the neurogenic regions of adult brain27. Moreover, flow cytometry and FACS can be exploited to quantify, analyze and isolate various cell populations including mature neurons54, astroglia33, microgl.......

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Disclosures

The authors declare no potential conflicts of interest.

Acknowledgements

Our research program is funded through the Emmy Noether-Program of the German Research Foundation (DFG), grant PR1132/3-1. Further support by the Müller-Fahnenberg Foundation of the University of Freiburg is gratefully acknowledged. This study was supported in part by the Excellence Initiative of the German Research Foundation (GSC-4, Spemann Graduate School).

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
DMEM/F12 (1:1) (Dulbecco's Modified Eagle Medium/Nutrient Mixture F-12)figure-materials-1 Life Technologies11330057
DPBS without Ca2+ Mg2+figure-materials-2 Life Technologies14190169
Fetal bovine serum, qualified, E.U.-approved, South America origin (FBS)figure-materials-3 Life Technologies10270-106
MEM Non-essential amino acids (100x)figure-materials-4 Life Technologies11140035
TrypLE Expressfigure-materials-5 Life Technologies12604013
Trypan blue solution, 0.4%figure-materials-6 Life Technologies15250061
Paraformaldehydefigure-materials-7 Carl Roth335.3
Bovine serum albumin (BSA) Fraction Vfigure-materials-8 PAA Laboratories, CoelbeK41-001
Tween-20 Detergentfigure-materials-9 Calbiochem655205
Carboxyfluorescein succinimidyl ester (CFSE)figure-materials-10 eBioscience65-0850-84
DMSOfigure-materials-11 AppliChemA1584
Bottle top filters express plus 0.22 µm, 250 mlfigure-materials-12 MilliporeSCGPU02RE
Cell culture treated flasks (T 25)figure-materials-13 NUNC156367
Cell culture treated flasks (T 75)figure-materials-14 NUNC156499
Conical tubes (15 ml)figure-materials-15 Greiner Bio-One188271
Conical tubes (50 ml)figure-materials-16 Greiner Bio-One227261
Pasteur pipet, glass (150 mm)figure-materials-17 STEIN Labortechnik, RemchingenS03710150
Pipet tips (0.1-10 µl)figure-materials-18 Corning4125
Pipet tips (1-200 µl)figure-materials-19 Corning4126
Pipet tips (100-1000 µl)figure-materials-20 Corning4129
Serological pipets, 5 mlfigure-materials-21 Corning4051
Serological pipets, 10 mlfigure-materials-22 Corning4101
Serological pipets, 25 mlfigure-materials-23 Corning4251
Microcentrifuge tubes (0.5 ml)figure-materials-24 Sarstedt72,699
Microcentrifuge tubes (1.5 ml)figure-materials-25 Greiner Bio-One616201
Microcentrifuge tubes (2.0 ml)figure-materials-26 Sarstedt72,695,500
Anti-Human CD24 APC monoclonal antibodyfigure-materials-27 eBioscience17-0247-42Working dilution 1:50
Anti-Human CD54 PE monoclonal antibodyfigure-materials-28 eBioscience12-0549-42Working dilution 1:50
Neuronal Class III β-Tubulin (Tuj1) polyclonal antibodyfigure-materials-29 CovancePRB-435PWorking dilution 1:2,000
Alexa Fluor 488 Donkey anti Rabbitfigure-materials-30 Life TechnologiesA21206Working dilution 1:2,000
Zenon® Fluorescein Rabbit IgG Labeling Kitfigure-materials-31 Life TechnologiesZ-25342
Neubauer-Improved counting chamberfigure-materials-32 Marienfeld0640010
Vortexfigure-materials-33 Scientific IndustriesG560E
Thermomixer comfortfigure-materials-34 Eppendorf5355 000.001
Accuri C6 flow cytometerfigure-materials-35 Becton Dickinson (BD)653118
Microcentrifuge refrigerated, PerfectSpin 24 Rfigure-materials-36 Peqlab91-PSPIN-24R
Orbital shaker, Unimax 1010figure-materials-37 Heidolph543-12310-00
Centrifuge refrigerated, Rotanta 96 RCfigure-materials-38 Hettich4480-50
Class II Biological safety cabinet Safe 2020figure-materials-39 Thermo Scientific51026640
CO2 Incubator, Heracell 240ifigure-materials-40 Thermo Scientific51026331
Vacuum system, Vacusafe comfortfigure-materials-41 Integra Biosciences158320
Microscope, Axiovert 40 CFLfigure-materials-42 Zeiss451212
Pipet controller, accu-jet profigure-materials-43 Brand26303
Micropipet, Pipetman neo P20N (2-20 µl)figure-materials-44 GilsonF144563
Micropipet, Pipetman neo P200N (20-200 µl)figure-materials-45 GilsonF144565
Micropipet, Pipetman neo P1000N (100-1000 µl)figure-materials-46 GilsonF144566

References

  1. Herzenberg, L. A., et al. The History and Future of the Fluorescence Activated Cell Sorter and Flow Cytometry: A View from. 48 (10), 1819-1827 (2002).
  2. Chattopadhyay, P. K., Roederer, M. Cytometry: today’s technology and tomorrow's horizons. <....

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