Method Article

Neutrophil Lifespan Extension with CLON-G and an In Vitro Spontaneous Death Assay

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DOI:

10.3791/65132

May 12th, 2023

* These authors contributed equally

In This Article

Summary

This protocol details the preparation of CLON-G to extend the neutrophil lifespan to greater than 5 days and provides a reliable procedure for evaluating neutrophil death with flow cytometry and confocal fluorescence microscopy.

Abstract

The average lifespan of a neutrophil is less than 24 h, which limits basic research on neutrophils and the application of neutrophil studies. Our previous research indicated that multiple pathways could mediate the spontaneous death of neutrophils. A cocktail was developed by simultaneously targeting these pathways, caspases-lysosomal membrane permeabilization-oxidant-necroptosis inhibition plus granulocyte colony-stimulating factor (CLON-G), which prolonged the neutrophil lifespan to greater than 5 days without significantly compromising the neutrophil function. Concurrently, a reliable and stable protocol for assessing and evaluating neutrophil death was also developed. In this work, we show that CLON-G can prolong the neutrophil lifespan in vitro to more than 5 days, and we exhibit the lengthening of the neutrophil lifespan with FACS and confocal fluorescence microscopy. This report introduces procedures for the preparation of CLON-G and showcases an in vitro spontaneous death assay of neutrophils, which can be used for the study of neutrophils and for subsequently interrogating neutrophil death, thus providing a reliable resource for the neutrophil community.

Introduction

Neutrophils are known to comprise an arsenal of abundant cytoplasmic granules, nicotinamide adenine dinucleotide phosphate (NADPH) oxidase, antimicrobial enzymes, and various organelles that defend against invading microbes; additionally, they are highly motile and are the first cells recruited to the inflammation site, meaning neutrophils are the first line of defense of the innate immune system1,2. Granulocyte transfusion therapy has hence become a promising clinical treatment for neutropenia-related infections to transiently boost neutrophil immunity3,4

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Protocol

The Boston Children's Hospital and State Key Laboratory of Experimental Hematology (SKLEH) Animal Care and Use Committee approved and monitored all the procedures. Figure 1 depicts a flow chart of neutrophil culturing with CLON-G and the in vitro death assay.

1. Neutrophil lifespan extension with CLON-G

NOTE: All the mentioned operations and materials must be sterile. Ensure all the solutions are well mixed and distributed evenly.

  1. Preservation of the CLON-G components
    1. Dissolve 50 mg of Q-VD-oph (see Table of Materials

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Results

The Wright-Giemsa-stained morphology (Figure 2A-D) and FACS phenotypes (Figure 2E-J) of the CLON-G treated neutrophils were not affected. The viability of the CLON-G treated neutrophils at 24 h was about 90%+ based on flow cytometry analysis (Figure 3) and the fluorescent image assays (Figure 4). Lower viability could result from improp.......

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Discussion

Neutrophils play vital roles in innate and adaptive immunity, and their homeostasis is tightly regulated. Neutrophils are the most abundant leukocytes in human peripheral blood, and they have a robust and fast turnover. A healthy adult can release 1 x 109 neutrophils/kg daily from the bone marrow28. The death of neutrophils has hence become one of the puzzling enigmas of this field, and much effort has been dedicated to better understanding them. Caspase29,<.......

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Disclosures

The authors declare that the research was conducted in the absence of any conflicts of interest.

Acknowledgements

This project was supported by the Haihe Laboratory of Cell Ecosystem Innovation Fund (22HHXBSS00036, 22HHXBSS00019), the Chinese Academy of Medical Sciences (CAMS) Innovation Fund for Medical Sciences (2021-I2M-1-040,2022-I2M-JB-015), the Special Research Fund for Central Universities, Peking Union Medical College (3332022062), and the Science and Technology Support Program of Sichuan Province (NO. 2021YJ0480).

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
0.2 µm syringe filterPall Corporation4612Filtrate prepared CLON-G components.
1.5 mL micro centrifuge tubeLABSELECTMCT-001-150Lab consumable.
15 mL Centrifuge TubesLABSELECTCT-002-15Lab consumable.
24 well cell culture plateFalcon351147Neutrophil culture plate.
50 mL Centrifuge TubesLABSELECTCT-002-50Lab consumable.
BD LSRIIBDInstrument for flow cytometry analysis of neutrophil death.
Calcium chloride (CaCl2)Sigma AldrichC4901Assitant of Annexin-V binding  to phosphatidylserine.
Confocal microscopePerkinelmerUltraVIEW VOXInstrument for fluorescent analysis of neutrophil death.
Confocal plateNEST801001-20mmLab consumable for fluorescent image assay.
Counting beadsThermo FisherC36950Quantification in flow cytometry analysis of neutrophil death.
DFOSigma AldrichD9533Component of CLON-G. LMP inhibitor.
Dimethyl sulfoxide ( DMSO)Sigma AldrichD2650Solvent for Q-VD-oph and Nec-1s.
Fetal Bovine SerumGibco10099141CComponent of neutrophil culture basic medium. Nutrition supply.
FITC-Annexin-VBD51-65874XAnnexin-V can bind to phosphatidylserine of aged cells.This is at FITC channel.
Hsp70Abcamab113187Component of CLON-G. LMP inhibitor.
NACSigma AldrichA9165Component of CLON-G. Antioxidant.
Nec-1sEMD Millipore852391-15-2Component of CLON-G. Necroptosis inhibitor.
Penicillin-Streptomycin Solution (PS)Gibco15070063Component of neutrophil culture basic medium. Antibiotics to protect cells from bacteria comtamination.
Propidium Iodide (PI)BioLegend421301For neutrophil death assay. A small fluorescent molecule that binds to DNA  but cannot passively traverse into cells that possess an intact plasma membrane.
Q-VD-ophSelleck chemS7311Component of CLON-G. Pan-caspase inhibitor.
Recombinant Human Granulocyte Colony-stimulating Factor for Injection (CHO cell)(G-CSF)Chugai Pharma ChinaGRANOCYTEComponent of CLON-G.  Promote neutrophil survival through Akt pathway.
Round-Bottom Polystyrene TubesFalcon100-0102Lab consumable for flow cytometry analysis.
RPMI1640GibcoC11875500BTComponent of neutrophil culture basic medium.
SalineLEAGENER00641Solution for flow cytometry analysis of neutrophil death.
Sodium hydroxide (NaOH)FENG CHUAN13-011-00029pH adjustion for NAC.
Wright-Giemsa Stain SolutionSolarbioG1020Neutrophil cytospin staining.

References

  1. Segal, A. W. How neutrophils kill microbes. Annual Review of Immunology. 23, 197-223 (2005).
  2. Rosales, C. Neutrophil: A cell with many roles in inflammation or several cell types. Frontiers in Physiology. 9, 113(2018).
  3. Chung, S., Armstrong-Scott, O.,....

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Tags

CLON G TreatmentNeutrophil PreservationFlow CytometryConfocal MicroscopyNeutrophil CultureCell ViabilityGranulocyte Colony Stimulating FactorAnnexin V Staining

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