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Method Article

Monitoring Gut Acidification in the Adult Drosophila Intestine

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DOI:

10.3791/63141

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October 11th, 2021

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In This Article

Summary

Here, we present a standardized protocol for monitoring gut acidification in Drosophila melanogaster with optimal output. We first use this protocol for gut acidification monitoring in Drosophila melanogaster and then demonstrate its use in non-model Drosophila species.

Abstract

The fruit fly midgut consists of multiple regions, each of which is composed of cells that carry out unique physiological functions required for the proper functioning of the gut. One such region, the copper cell region (CCR), is localized to the middle midgut and consists, in part, of a group of cells known as copper cells. Copper cells are involved in gastric acid secretion, an evolutionarily conserved process whose precise role is poorly understood. This paper describes improvements in the current protocol used to assay for acidification of the adult Drosophila melanogaster gut and demonstrates that it can be used on other species of flies. In particular, this paper demonstrates that gut acidification is dependent on the fly's nutritional status and presents a protocol based on this new finding. Overall, this protocol demonstrates the potential usefulness of studying Drosophila copper cells to uncover general principles underlying the mechanisms of gut acidification.

Introduction

In the insect gut, copper cells share cellular and functional similarities with the acid-producing gastric parietal cells (also known as oxyntic) of the mammalian stomach. This group of cells releases acid into the intestinal lumen. The function of acid secretion and anatomy is evolutionarily conserved. The major components of the discharged acid are hydrochloric acid and potassium chloride. The chemical mechanism of acid formation in the cells depends on carbonic anhydrase. This enzyme generates a bicarbonate ion from CO2 and water, which liberates a hydroxyl ion that is then discharged into the lumen through a proton pump in exchange for potassium. Chlori....

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Protocol

NOTE: The standard laboratory line Oregon R was used as a WT control. All flies were reared on standard cornmeal-molasses medium (containing molasses, agar, yeast, cornmeal, tegosept, propionic acid, and water) at room temperature with 12/12 h light/dark circadian rhythm.

1. Preparing for the assay

  1. Collect female flies (0-2 days old, non-virgin) under CO2 anesthesia and allow them to recover on standard cornmeal food for at least 3 days before experiments.
  2. Starve the flies for ~24 h at room temperature (~23 °C) in vials containing a laboratory wipe tissue soaked with ~2 mL of deionized ....

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Results

We starved Oregon R female flies for more than 20 h and then fed them food supplemented with BPB (2%) for ~12 h, as described previously7,8,9,10,11. Bromophenol blue (BPB) is a pH-sensing dye. It changes from yellow at pH 3.0 to blue at pH 4.6 and above. Following gut dissection, as previously reported, some flies were found to produce acid as indicated by yel.......

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Discussion

A critical step in this protocol is the proper dissection of the gut to visualize the CCR for the acidification phenotype. The acid released from the copper cells is confined to the CCR when the gut is intact. However, during dissection, leakage caused by rupture of the intestine can lead to diffusion of acid from the CCR and result in a gut mistakenly scored as a negative for acidification. In addition, the yellow color indicative of acidification fades within 5-10 min after dissection, underscoring the importance of sc.......

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Disclosures

The authors have no conflicts of interest to disclose.

Acknowledgements

The authors acknowledge that support for work in the author's laboratory is provided by an HHMI Faculty Scholar Award and startup funds from the Children's Research Institute at UT Southwestern Medical Center.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Bromophenol blueSigma-AldrichB0126
cellSens softwareOlympusImage aqusition (https://www.olympus-lifescience.com/en/software/cellsens)
D. simulansDrosophila Species Stock Center at the University of CaliforniaRiverside California1 (https://www.drosophilaspecies.com/)
D. erectaDrosophila Species Stock Center at the University of CaliforniaDere cy1(https://www.drosophilaspecies.com/)
D. pseudoobscuraDrosophila Species Stock Center at the University of CaliforniaEugene, Oregon(https://www.drosophilaspecies.com/)
D. mojavensisDrosophila Species Stock Center at the University of CaliforniaChocolate Mountains, California (https://www.drosophilaspecies.com/)
ForcepsInox BiologyCatalog# 11252-20
FujiFujiImage processing (https://hpc.nih.gov/apps/Fiji.html)
Glass slideVWRCatalog#16005-108
Kim wipes TissueKimtech
Microscope and cameraOlympus SZ61 microscope equipped with an Olympus D-27 digital cameraImaging
Oregon RBloomington Drosophila Stock(https://bdsc.indiana.edu/ # 2376)
Petri dishesFisher ScientificCatalog #FB0875713A
Phosphate-buffered Saline (PBS)HyCloneCatalog # SH30258.01
StereomicroscopeOlympus SZ51Visual magnification

References

  1. Hollander, F. The composition and mechanism of formation of gastric acid secretion. Science. 110 (2846), 57-63 (1949).
  2. Forte, J. G., Zhu, L. Apical recycling of the gastric parietal cell H, K-ATPase. Annual Review of Physiology. 72, 273-296 (2010).

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Copper CellsGastric Acid SecretionBromophenol BlueNutritional StatusFly DissectionPetri Dish AssayStereo MicroscopeAcidification Protocol