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Method Article

An Optical Assay for Synaptic Vesicle Recycling in Cultured Neurons Overexpressing Presynaptic Proteins

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DOI:

10.3791/58043

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June 26th, 2018

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In This Article

Summary

We describe an optical assay for synaptic vesicle (SV) recycling in cultured neurons. Combining this protocol with double transfection to express a presynaptic marker and protein of interest allows us to locate presynaptic sites, their synaptic vesicle recycling capacity, and determine the role of the protein of interest.

Abstract

At active presynaptic nerve terminals, synaptic vesicles undergo cycles of exo- and endocytosis. During recycling, the luminal domains of SV transmembrane proteins become exposed at the cell surface. One of these proteins is Synaptotagmin-1 (Syt1). An antibody directed against the luminal domain of Syt1, once added to the culture medium, is taken up during the exo-endocytotic cycle. This uptake is proportional to the amount of SV recycling and can be quantified through immunofluorescence. Here, we combine Syt1 antibody uptake with double transfection of cultured hippocampal neurons. This allows us to (1) localize presynaptic sites based on expression of recombinant presynaptic marker Synaptophysin, (2) determine their functionality using Syt1 uptake, and (3) characterize the targeting and effects of a protein of interest, GFP-Rogdi.

Introduction

Studying synaptic vesicle recycling is important in determining how presynaptic properties change, either during synaptic plasticity or in response to perturbation of synaptic function. Studying Synaptotagmin-1 (Syt1) antibody uptake provides one method of measuring the amount of SV recycling. Syt1 is a SV-associated protein that acts as a Ca2+ sensor and is necessary for exocytotic release of the neurotransmitter1,2. It is a transmembrane protein with a C-terminal cytoplasmic domain outside the SV and an N-terminal luminal domain inside the SV3. During exocytosis, the lumina....

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Protocol

No studies with live animals were conducted. Experiments involving euthanized animals to obtain cell cultures were approved by the local animal protection authorities (Tierschutzkommission der Universitätsmedizin Göttingen) under the approval number T10/30. The experiments were conducted with the approved protocols.

1. Primary Hippocampal Cell Culture

  1. Prepare the dissociated cell culture of the rat hippocampus on embryonic day 1916,17. Plate the cells on 12 mm coverslips coated with polyethyleneimine (PEI) in 24-well dishes at a density of 50,000 - 60,000 cells....

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Results

An expected result of this approach is locating approximately 50 double-transfected neurons per coverslip at a density of 50,000 neurons per well. The axon of each neuron is expected to show multiple hotspots of fluorescently-tagged Synaptophysin accumulation, indicating clusters ofSVs. At functional presynaptic sites, the recombinant Synaptophysin signal colocalizes with punctate Syt1 fluorescence. Using double transfection, either GFP-Rogdi as the protein of interest (

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Discussion

There are three assays routinely used to study synaptic vesicle (SV) recycling. The first two include the use of a) fluorescent styryl dyes such as FM1-43 (which incorporate into membranes, are taken up into organelles during endocytosis, and are released after exocytosis); and b) fluorescently tagged recombinant SV proteins (which, upon overexpression, incorporate into the proteinaceous recycling machinery). If the attached fluorophores change their fluorescence depending on the pH, they can be used to monitor changes b.......

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Disclosures

The authors have nothing to disclose.

Acknowledgements

We thank Irmgard Weiss for expert technical assistance. This work was supported by the DFG via the Cluster of excellence for microscopy at the nanometer range and molecular physiology of the brain (CNMPB, B1-7, to T.D.).

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
B27Gibco17504-044
BSASigmaA7030-50g
CaCl2Sigma-AldrichC3306-100g
CoolSNAP HQ2Photometrics
dH2OInvitrogen15230
DABCOMerck8.03456.0100
donkey anti mouse Alexa 647Jackson-Immunoresearch715605151antibody
DMEMInvitrogen41966
DPBSGibco14190
Eppendorf tubesEppendorf30120094
multiwell 24 wellFisher Scientific087721H
tube (50 mL)Greiner Bio-One227261
FBS superiorBiochromAGS0615
GlucoseMerck1,083,421,000
HBSSInvitrogen14170
HEPESSigmaH4034-500g
Hera Cell 150 (Inkubator)ThermoElectron Corporation
KCLSigma-AldrichP9541-500g
L-GlutaminGibco25030
MgCl2HoneywellM0250-500g
microscope slidesFisher Scientific10144633CF
Microsoft ExcelMicrosoft
Mowiol4-88Calbiochem475904
NaClBioFroxx1394KG001
Na2HPO4BioFroxx5155KG001
NeurobasalInvitrogen21103049
OpenView Experiment Analysis ApplicationFree software, see commentswritten by Noam E. Ziv, Technion – Israel Institute of Technology, Haifa, Israel
PBS (10x)Roche11666789001
OptimemInvitrogen31985
PenstrepGibco15140-122
PFASigmaP6148-1kg
safety hoodThermoElectronSerial No. 40649111
SucroseneoFroxx1104kg001
Synaptotagmin1Synaptic Systems105311mouse monoclonal; clone 604.2
Triton X-100Merck1,086,031,000
Vortex Genius 3 IKA3340001
Water bathGFL1004
Zeiss Observer. Z1 Zeiss

References

  1. Koh, T., Bellen, H. J. Synaptotagmin I, a Ca2+ sensor for neurotransmitter release. Trends in Neurosciences. 26, 413-422 (2003).
  2. Chapman, E. R. How Does Synaptotagmin Trigger Neurotransmitter Release. Annual Review of Biochemistry. 77, 615-6....

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