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In This Article

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

Summary

Here we describe an in vitro live-imaging method to visualize intracellular transport of organelles and trafficking of plasma membrane proteins in murine astrocytes. This protocol also presents an image analysis methodology to determine cargo transport itineraries and kinetics.

Abstract

Astrocytes are among the most abundant cell types in the adult brain, where they play key roles in a multiplicity of functions. As a central player in brain homeostasis, astrocytes supply neurons with vital metabolites and buffer extracellular water, ions, and glutamate. An integral component of the “tri-partite” synapse, astrocytes are also critical in the formation, pruning, maintenance, and modulation of synapses. To enable these highly interactive functions, astrocytes communicate among themselves and with other glial cells, neurons, the brain vasculature, and the extracellular environment through a multitude of specialized membrane proteins that include cell adhesion molecules, aquaporins, ion channels, neurotransmitter transporters, and gap junction molecules. To support this dynamic flux, astrocytes, like neurons, rely on tightly coordinated and efficient intracellular transport. Unlike neurons, where intracellular trafficking has been extensively delineated, microtubule-based transport in astrocytes has been less studied. Nonetheless, exo- and endocytic trafficking of cell membrane proteins and intracellular organelle transport orchestrates astrocytes’ normal biology, and these processes are often affected in disease or in response to injury. Here we present a straightforward protocol to culture high quality murine astrocytes, to fluorescently label astrocytic proteins and organelles of interest, and to record their intracellular transport dynamics using time-lapse confocal microscopy. We also demonstrate how to extract and quantify relevant transport parameters from the acquired movies using available image analysis software (i.e., ImageJ/FIJI) plugins.

Introduction

Astrocytes are the most abundant cells in the adult central nervous system, where they perform unique developmental and homeostatic functions1. Astrocytes modulate synaptic development through direct contact with pre- and postsynaptic terminals as part of the tri-partite synapse, which contains neurotransmitter receptors, transporters, and cell adhesion molecules that facilitate synapse formation and neuron-astrocyte communication2. In addition, astrocytes actively control synaptic transmission and prevent neuronal excitotoxicity by rapidly removing excitatory neurotransmitters from the synaptic cleft, recycling neurotra....

Protocol

All animal procedures were performed with the approval of the University of North Carolina at Chapel Hill Animal Care and Use Committee (IACUC).

1. Brain dissection and culture of primary mouse astrocytes

NOTE: The following protocol was adapted from published methods, which follows the original procedure developed by McCarthy and deVellis13,14,15. Mixed cell cultures of McCa.......

Representative Results

The protocol for establishing primary mouse MD astrocytes outlined above should yield reproducible, high quality cultures. Although cultures initially contain a mix of astrocytes, fibroblasts, and other glial cells, including microglia and oligodendrocytes (Figure 1Bi,Biv; red arrowheads), the addition of AraC to the mixed culture between DIV5-DIV7 minimizes the proliferation of these contaminant cells. The combined AraC treatment and shaking-based purification strategy enri.......

Discussion

Here, we describe an experimental approach to express, visualize, and track fluorescently tagged organelles and membrane proteins of interest using time-lapse video microscopy in high-purity primary mouse cortical MD astrocytes. We also outline a methodology for measuring particle dynamics. Direct visualization of protein and organelle dynamics in primary astrocytes provides a powerful tool to study the regulation of intracellular transport in these cells in vitro.

The methodology for establis.......

Acknowledgements

DNL was supported by the University of North Carolina at Chapel Hill (UNC) School of Medicine as a Simmons Scholar. TWR was supported by UNC PREP Grant R25 GM089569. Work using the UNC Neuroscience Center Microscopy Core Facility was supported, in part, by funding from the NIH-NINDS Neuroscience Center Support Grant P30 NS045892 and the NIH-NICHD Intellectual and Developmental Disabilities Research Center Support Grant U54 HD079124.

....

Materials

NameCompanyCatalog NumberComments
2.5% Trypsin (10x)Gibco15090-046
Benchtop CentrifugeThermo Scientific75-203-637Sorvall ST8 Centrifuge
Cell Culture Grade WaterGen Clone25-511
Cell Culture MicroscopeZeissWSN-AXIOVERT A1Vert.A1 inverted scope, Inverted tissue culture microscope with fluorescent capabilities
Cytosine ArabinosideSigmaC1768-100MG(AraC) Dissolve lyophilized powder in sterile cell culture grade water to make a 10mM stock, aliquot and freeze for long term storage
DAPISigmaD9542-5MGDissolve lyophilized powder in deionized water to a maximum concentration of 20 mg/ml, heat or sonicate as necessary. Use at 300 nM for counterstaining.
Dissecting MicroscopeZeissStemi 305
Dissecting ScissorsF.S.T14558-09
Dulbecco's Modified Eagle MediumGen Clone25-500
Fetal Bovine SerumGemini100-106Heat-Inactivated
FIJI (Fiji is Just Image J)NIHVersion 1.52i
Fine Tip TweezersF.S.T11254-20Style #5
Fluorescence light sourceExcelitas012-63000X-Cite 120Q
GFAP antibodyCell Signaling3670SGFAP (GA5) mouse monoclonal antibody
Glass Bottom DishesMattek corporationP35G-1.5-14-C35 mm Dish | No. 1.5 Coverslip | 14 mm Glass Diameter | Uncoated
Graefe ForcepsF.S.T11054-10Graefe Iris Forceps with curved tips
Green fluorescent dye that stains acidic compartments (late endosomes and lysosomes)Life TechnologiesL7526LysoTracker Green DND 26. Pre-dissolved in DMSOS to a 1mM stock solution. Dilute to the final working concentration in the growth medium or buffer of choice.
Hank's Balanced Salt Solution (10x)Gibco14065-056Magnesium and calcium free
Imaging MediaLife TechnologiesA14291DJLive Cell Imaging Solution
Inverted Confocal MicroscopeZeissLSM 780
KymoToolBoxhttps://github.com/fabricecordelieres/IJ_KymoToolBox
Lipofection Enhancer ReagentLife Technologies11514015Plus Reagent
Lipofection ReagentLife Technologies15338100Lipofectamine LTX reagent
Orbital shaking incubatorNew Brunswick Scientific8261-30-1008Innova 4230 , orbital shaking incubator with temperature and speed control
Penicillin/Strepomycin solution (100x)Gen Clone25-512
Phosphate Buffered Saline (10x)Gen Clone25-507x
Poly-D-Lysine HydrobromideSigmaP7405Dissolve in Tris buffer, pH 8.5, at 1mg/mL. Freeze for long term storage. Avoid cycles of freezing and thawing
Reduced serum mediumGibco31985-062OPTI-MEM
Tissue Culture FlasksOlympus Plastics25-20975 cm^2. 100% angled neck access, 0.22um hydrophobic vented filter cap
Tissue culture incubatorThermo Scientific51030285HERAcell VIOS 160i, tissue culture incubator with temperature, humidity, and CO2 control
Tris-BaseSigmaT15038.402 g dissolved to one liter in water with 4.829 g Tris HCl to make 0.1 M Tris buffer, pH 8.5
Tris-HClSigmaT32534.829 g dissolved to one liter in water with 8.402 g Tris Base to make 0.1 M Tris buffer, pH 8.5
Trypsin-EDTA (0.25%), phenol redGibco25200072
Vacuum-Driven Filter SystemsOlympus Plastics25-227500 ml, PES membrane, 0.22 µm
Vannas scissors straightRobozRS-5620

References

  1. Barres, B. A. The mystery and magic of glia: a perspective on their roles in health and disease. Neuron. 60 (3), 430-440 (2008).
  2. Araque, A., Parpura, V., Sanzgiri, R. P., Haydon, P. G. Tripartite synapses: Glia, the u....

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