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In This Article

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

Summary

We describe a protocol to label macrophage-derived small extracellular vesicles with PKH dyes and observe their uptake in vitro and in the spinal cord after intrathecal delivery.

Abstract

Small extracellular vesicles (sEVs) are 50-150 nm vesicles secreted by all cells and present in bodily fluids. sEVs transfer biomolecules such as RNA, proteins, and lipids from donor to acceptor cells, making them key signaling mediators between cells. In the central nervous system (CNS), sEVs can mediate intercellular signaling, including neuroimmune interactions. sEV functions can be studied by tracking the uptake of labeled sEVs in recipient cells both in vitro and in vivo. This paper describes the labeling of sEVs from the conditioned media of RAW 264.7 macrophage cells using a PKH membrane dye. It shows the uptake of different concentrations of labeled sEVs at multiple time points by Neuro-2a cells and primary astrocytes in vitro. Also shown is the uptake of sEVs delivered intrathecally in mouse spinal cord neurons, astrocytes, and microglia visualized by confocal microscopy. The representative results demonstrate time-dependent variation in the uptake of sEVs by different cells, which can help confirm successful sEVs delivery into the spinal cord.

Introduction

Small extracellular vesicles (sEVs) are nanosized, membrane-derived vesicles with a size range of 50-150 nm. They originate from multi-vesicular bodies (MVBs) and are released from cells upon fusion of the MVBs with the plasma membrane. sEVs contain miRNAs, mRNAs, proteins, and bioactive lipids, and these molecules are transferred between cells in the form of cell-to-cell communication. sEVs can be internalized by recipient cells by a variety of endocytic pathways, and this capture of sEVs by recipient cells is mediated by the recognition of surface molecules on both EVs and the target cells1.

sEVs have gained intere....

Protocol

NOTE: All procedures were performed in compliance with the NIH Guide for the Care and Use of Laboratory Animals and approved by the Institutional Animal Care & Use Committee of Drexel University College of Medicine. Timed-pregnant CD-1 mice were used for astrocytic culture, and all dams were received 15 days after impregnation. Ten-twelve weeks old C57BL/6 mice were used for in vivo uptake experiments.

1. Isolation of sEVs from RAW 264.7 macrophage cells

  1. Culture RAW 264.7 cells in 75 cm2 flasks in DMEM exosome-depleted medium containing 10% exosome-depleted fetal bovine serum (FBS) and 1% penicillin-strep....

Representative Results

After the isolation of sEVs from RAW 264.7 conditioned media via centrifugation, NTA was used to determine the concentration and size distribution of the purified sEVs. The average mean size of RAW 264.7-derived sEVs was 140 nm, and the peak particle size was 121.8 nm, confirming that most detectable particles in the light scattering measurement fell within the size range of exosomes or sEVs at 50-150 nm (Figure 1A). As suggested in the minimal information for studies of extracellular vesicl.......

Discussion

In this protocol, we showed the labeling of sEVs with PKH dyes and the visualization of their uptake in the spinal cord. PKH lipophilic fluorescent dyes are widely used for labeling cells by flow cytometry and fluorescent microscopy3,5,6,12,24,25. Due to their relatively long half-life and low cytotoxicity, PKH dyes can be us.......

Disclosures

The authors have no conflicts of interest to disclose.

Acknowledgements

This study was supported by grants from NIH NINDS R01NS102836 and the Pennsylvania Department of Health Commonwealth Universal Research Enhancement (CURE) awarded to Seena K. Ajit. We thank Dr. Bradley Nash for critical reading of the manuscript.

....

Materials

NameCompanyCatalog NumberComments
Amicon Ultra 0.5 mL centrifugal filtersMilliporeSigmaZ677094
Anti-Alix AntibodyAbcamab1864291:1000
Anti-Calnexin AntibodyAbcamAb102861:1000
Anti-CD81 AntibodySanta Cruz Biotechnologysc-1660291:1000
Anti-GAPDH Monoclonal Antibody (14C10)Cell Signaling Technology21181:1000
Anti-Glial Fibrillary Acidic Protein AntibodySigma-AldrichMAB3601:500 for IF; 1:1000 for IHC
Anti-Iba1 AntibodyWako019-197411:2000
Anti-MAP2A AntibodySigma-AldrichMAB3781:500
Bovine Serum Albumin (BSA)VWR0332
Cell Strainer, 40 μmVWR15-1040-1
Centrifuge TubesThermo Scientific3118-005012,000 x g
Coverslip, 12-mm, #1.5Electron Microscopy Sciences72230-01
Coverslip, 18-mm, #1.5Electron Microscopy Sciences72222-01
DAPISigma-AldrichD9542-1MG1 µg/mL
DC Protein AssayBio-Rad500-0116
Deoxyribonuclease I (DNAse I)MilliporeSigmaD4513-1VL
Donkey Anti-Rabbit IgG H&L (HRP)Abcamab162841:10000
Donkey Anti-Rabbit IgG H&L, Alexa Fluor 488InvitrogenA-212061:500
Double Frosted Microscope Slides, #1Thermo Scientific12-552-5
DPBS without Calcium and MagnesiumCorning21-031-CV
Dulbecco's Modified Eagle Medium (DMEM)Corning10-013-CV
Exosome-Depleted Fetal Bovine SerumGibcoA27208-01
Fetal Bovine Serum (FBS)Corning35-011-CV
FluorChem M imaging systemProteinSimple
FV3000 Confocal MicroscopeOlympus
Goat Anti-Mouse IgG H&L (HRP)Abcamab67891:10000
Goat Anti-Mouse IgG H&L, Alexa Fluor 488InvitrogenA-110011:500
Goat Anti-Mouse IgG1, Alexa Fluor 594InvitrogenA-21125
Hank's Balanced Salt Solution (HBSS)VWR02-0121
HEPESGibco15630080
HRP SubstrateThermo Scientific34094
Intercept blocking buffer, TBSLI-COR Biosciences927-60001
Laemmli SDS Sample BufferAlfa AesarAAJ61337AC
Micro Cover Glass, #1VWR48404-454
Microm HM550Thermo Scientific
NanoSight NS300 systemMalvern Panalytical
NanoSight NTA 3.2 softwareMalvern Panalytical
Neuro-2a Cell LineATCCCCL-131
Normal Goat SerumVector LaboratoriesS-1000
O.C.T CompoundSakura Finetek4583
PapainWorthington Biochemical CorporationNC9597281
ParaformaldehydeElectron Microscopy Sciences19210
Penicillin-StreptomycinGibco15140122
PKH26Sigma-AldrichMINI26-1KT
PKH67Sigma-AldrichMINI67-1KT
Protease Inhibitor CocktailThermo Scientific1862209
PVDF Transfer MembraneMDISVFX8302XXXX101
RAW 267.4 Cell LineATCCTIB-71
RIPA BufferSigma-AldrichR0278
Sodium ChlorideAMRESCO0241-2.5KG
Superfrost Plus Gold SlidesThermo Scientific15-188-48adhesive slides
T-75 FlasksCorning431464U
Tecnai 12 Digital Transmission Electron MicroscopeFEI Company
TEM GridsElectron Microscopy SciencesFSF300-cu
Tris-Glycine Protein Gel, 12%InvitrogenXP00120BOX
Tris-Glycine SDS Running BufferInvitrogenLC26755
Tris-Glycine Transfer BufferInvitrogenLC3675
TrypLE Expresscell dissociation enzyme
Triton X-100Acros Organics327371000
Trypsin, 0.25%Corning25-053-CL
Tween 20
Ultracentrifuge TubesBeckman344058110,000 x g

References

  1. Mulcahy, L. A., Pink, R. C., Carter, D. R. F. Routes and mechanisms of extracellular vesicle uptake. Journal of Extracellular Vesicles. 3 (1), 24641 (2014).
  2. Betzer, O., et al. Advances in imaging strategies for in vivo tracking of exos....

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