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In This Article

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

Summary

Here we present a protocol to visualize the transport of monocarboxylates, glucose, and ATP in glial cells and neurons using genetically encoded Förster resonance energy transfer-based sensors in an ex-vivo Drosophila larval brain preparation.

Abstract

The high energy requirements of brains due to electrical activity are one of their most distinguishing features. These requirements are met by the production of ATP from glucose and its metabolites, such as the monocarboxylates lactate and pyruvate. It is still unclear how this process is regulated or who the key players are, particularly in Drosophila.

Using genetically encoded Förster resonance energy transfer-based sensors, we present a simple method for measuring the transport of monocarboxylates and glucose in glial cells and neurons in an ex-vivo Drosophila larval brain preparation. The protocol describes how to dissect and adhere a larval brain expressing one of the sensors to a glass coverslip.

We present the results of an entire experiment in which lactate transport was measured in larval brains by knocking down previously identified monocarboxylate transporters in glial cells. Furthermore, we demonstrate how to rapidly increase neuronal activity and track metabolite changes in the active brain. The described method, which provides all necessary information, can be used to analyze other Drosophila living tissues.

Introduction

The brain has high energy requirements due to the high cost of restoring ion gradients in neurons caused by neuronal electric signal generation and transmission, as well as synaptic transmission1,2. This high energy demand has long been thought to be met by the continuous oxidation of glucose to produce ATP3. Specific transporters at the blood-brain barrier transfer the glucose in the blood to the brain. Constant glycemic levels ensure that the brain receives a steady supply of glucose4. Interestingly, growing experimental evidence suggests that molecules derived....

Protocol

1. Fly strain maintenance and larval synchronization

  1. To perform these experiments, use fly cultures raised at 25 °C on standard Drosophila food composed of 10% yeast, 8% glucose, 5% wheat flour, 1.1% agar, 0.6% propionic acid, and 1.5% methylparaben.
  2. To follow this protocol, use the following lines: w1118 (experimental control background), OK6-GAL4 (driver for motor neurons), repo-GAL4 (driver for all glial cells), CG-GAL4 (driver for fat bodies), U.......

Representative Results

For up to 1 h, this procedure allows for easy measurement of intracellular changes in the fluorescence of monocarboxylate and glucose sensors. As shown in Figure 4, Laconic sensors in both glial cells and motor neurons respond to 1 mM lactate at a similar rate at the start of the pulse, but motor neurons reach a higher increase over the baseline during the 5 min pulse, as previously demonstrated17. This lactate concentration was chosen because it is comparable to the .......

Discussion

The use of the Drosophila model for the study of brain metabolism is relatively new26, and it has been shown to share more characteristics with mammalian metabolism than expected, which has primarily been studied in vitro in primary neuron cultures or brain slices. Drosophila excels at in vivo experiments thanks to the battery of genetic tools and genetically encoded sensors available that allows researchers to visualize in real time the metabolic changes caused.......

Acknowledgements

We thank all the members of the Sierralta Lab. This work was supported by FONDECYT-Iniciación 11200477 (to AGG) and FONDECYT Regular 1210586 (to JS). UAS-FLII12Pglu700µδ6 (glucose sensor) was kindly donated by Pierre-Yves Plaçais and Thomas Preat, CNRS-Paris.

....

Materials

NameCompanyCatalog NumberComments
AgaroseSigmaA9539
CaCl2SigmaC3881
CCD Camera ORCA-R2Hamamatsu-
Cell-R SoftwareOlympus-
CG-GAL4Bloomington Drosophila Stock Center7011Fat body driver
Dumont # 5 ForcepsFine Science Tools11252-30
DV2-emission splitting systemPhotometrics-
Glass coverslips (25 mm diameter)Marienfeld111650Germany
GlucoseSigmaG8270
GraphPad PrismGraphPad SoftwareVersion 8,0,2
HEPESSigmaH3375
ImageJ softwareNational Institues of HealthVersion 1,53t
KClSigmaP9541
LUMPlanFl 40x/0.8 water immersion objectiveOlympus-
MethylparabenSigmaH5501
MgCl2SigmaM1028
NaClSigmaS7653
OK6-GAL4Bloomington Drosophila Stock CenterMotor neuron driver
PicrotoxinSigmaP1675SCAUTION-Fatal if swallowed
Poly-L-lysineSigmaP4707
Propionic AcidSigmaP1386
Repo-GAL4Bloomington Drosophila Stock Center7415Glial cell driver (all)
Sodium LactateSigma71718
Sodium pyruvateSigmaP2256
Spinning Disk fluorescence Microscope BX61WIOlympus-
SucroseSigmaS0389
TrehaloseUS BiologicalT8270
UAS-AT1.03NL Kyoto Drosophila Stock Center117012ATP sensor
UAS-Chk RNAi GD1829Vienna Drosophila Resource Centerv37139Chk RNAi line
UAS-FLII12Pglu700md6 Bloomington Drosophila Stock Center93452Glucose sensor
UAS-GCaMP6f Bloomington Drosophila Stock Center42747Calcium sensor
UAS-LaconicSierralta Lab-Lactate sensor
UAS-PyronicPierre Yves Placais/Thomas Preat-CNRS-Paris
UMPlanFl 20x/0.5 water immersion objectiveOlympus-

References

  1. Vergara, R. C., et al. The energy homeostasis principle: neuronal energy regulation drives local network dynamics generating behavior. Frontiers in Computational Neuroscience. 13 (49), 1-18 (2019).
  2. Pulido, C., Ryan, T. A.

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