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Method Article

Generation and Long-term Maintenance of Nerve-free Hydra

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DOI:

10.3791/56115

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July 7th, 2017

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In This Article

Summary

Through a double treatment with colchicine, a plant-derived toxin that kills dividing cells, nerve-free Hydra vulgaris can be generated. These Hydra cannot feed or egest on their own. This paper describes an improved method for long-term maintenance of nerve free Hydra vulgaris in the laboratory.

Abstract

The interstitial cell lineage of Hydra includes multipotent stem cells, and their derivatives: gland cells, nematocytes, germ cells, and nerve cells. The interstitial cells can be eliminated through two consecutive treatments with colchicine, a plant-derived toxin that kills dividing cells, thus erasing the potential for renewal of the differentiated cells that are derived from the interstitial stem cells. This allows for the generation of Hydra that lack nerve cells. A nerve-free polyp cannot open its mouth to feed, egest, or regulate osmotic pressure. Such animals, however, can survive and be cultured indefinitely in the laboratory if regularly force-fed and burped. The lack of nerve cells allows for studies of the role of the nervous system in regulating animal behavior and regeneration. Previously published protocols for nerve-free Hydra maintenance involve outdated techniques such as mouth-pipetting with hand-pulled micropipette tips to feed and clean the Hydra. Here, an improved protocol for maintenance of nerve-free Hydra is introduced. Fine-tipped forceps are used to force open the mouth and insert freshly killed Artemia. Following force-feeding, the body cavity of the animal is flushed with fresh medium using a syringe and hypodermic needle to remove undigested material, referred to here as "burping". This new method of force-feeding and burping nerve-free Hydra through the use of forceps and syringes eliminates the need for mouth-pipetting using hand-pulled micropipette tips. It thus makes the process safer and significantly more time efficient. To ensure that the nerve cells in the hypostome have been eliminated, immunohistochemistry using anti-tyrosine-tubulin is conducted.

Introduction

The nervous system of Hydra consists of a nerve net, with neurons associated with both epithelial tissue layers1. The nerve net is denser in the hypostome and peduncle and less dense in the body column2. The nerve cells originate from interstitial stem cells, which are multipotent stem cells that give rise to secretory cells, nematocytes, germ cells, and neurons1. It is possible to eliminate the interstitial cells of Hydra vulgaris through treatment with colchicine3,4, a plant-derived toxin that kills dividing cells. Alth....

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Protocol

1. Double Colchicine Treatment

  1. Make a 0.4% colchicine (weight/volume) solution in Hydra medium3,4,17.
    Caution: Colchicine is acutely toxic, fatal if swallowed, may cause genetic defects, and may cause eye damage. Handle the powder in a fume hood and wear full Personal Protective Equipment (PPE).
  2. Incubate Hydra vulgaris (AEP strain was used here) that have been starved for 24 h in 0.4% colchicine at a ratio of 5 Hydra per mL of colchicine solution in a Petri dish for 8 h at room temperature in the dark.

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Results

Immediately following the initial 8 h colchicine treatment, all Hydra survive. Some of these Hydra will have only tentacle stubs remaining (Figure 3A), while others will have completely lost their tentacles (Figure 3B). Over the following 1 or 2 days, the tentacles will continue to shrink until all Hydra have lost their tentacles. About 1 week following the treatment, t.......

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Discussion

Hydra interstitial cells can be eliminated through a double colchicine treatment3,4. In the days following the first treatment, it is critical to prevent contact between individual Hydra to avoid fusion of Hydra pieces into deformed Hydra. Also, animals that can eat unassisted following the first treatment must be removed as the second colchicine treatment may not be sufficient to eliminate the remaining interstitial cells from.......

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Disclosures

The authors have nothing to disclose.

Acknowledgements

The authors thank Dr. Dick Campbell (UC Irvine) for discussions about the original protocol for generating and maintaining nerve-free animals, Ms. Rui Wang for help with adapting the syringe and needle technique, and Ms. Danielle Hagstrom and Dr. Rob Steele (UC Irvine) for comments on the manuscript. This work was supported by the RCSA and NSF grant CMMI-1463572.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
ColchicineAcros Organics227120010
1 mL SyringeBD301025
Brine Shrimp EggsBrine Shrimp DirectN/ACan be purchased locally
Brine Shrimp Hatchery DishBrine Shrimp DirectN/A
60 mm x 15 mm Petri DishCelltreat229663
30 G x 3/4" Hypodermic NeedleCovidien1188830340A 27G needle may also be used
2 x Fine-tip TweezersDumont0109-5-PO
RifampicinEMD Millipore557303
Goat anti-mouse lgG, Pab (HRP Conjugate)EnzoADI-SAB-100-J
Bovine Serum Albumin (BSA)FisherBP9703-100
ScalpelFisher08-920A
Fetal Bovine Serum (FBS)Gibco10437028
DAPI (4',6-Diamidino-2-Phenylindole, Dihydrochloride)InvitrogenD1306
PBS TabletsMP Bio2810305
Monoclonal Anti-Tubulin, TyrosineSigmaT9028
Dimethyl Sulfoxide (DMSO)SigmaD2650
Hydrogen PeroxideSigma216763
Paraformaldehyde (PFA)SigmaP6148
Triton X - 100SigmaT9284
Tween 20SigmaP1379
UrethaneSigmaU2500
Air PumpTetra77846-00
Glass Pasteur PipetteVWR53283-916Length of the pipet does not matter
15 mL TubeVWR89039-670
P320 Sandpaper3MIBGABBV00397Can be purchased at local home improvement store

References

  1. Bode, H. R. The interstitial cell lineage of Hydra: a stem cell system that arose early in evolution. J. Cell. Sci. 109, 1155-1164 (1996).
  2. Hager, G., David, C. N. Pattern of differentiated nerve cells in hydra is determined by precursor migratio....

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Force FeedingBurping TechniqueInterstitial Cell LineageColchicine TreatmentImmunohistochemistryTyrosine-tubulin StainingArtemia FeedingHypostome ManipulationRifampicin Supplementation