- Open Access
A view to kill
© Holstein; licensee BioMed Central Ltd. 2012
- Received: 21 February 2012
- Accepted: 5 March 2012
- Published: 5 March 2012
Genome and proteome data from Hydra magnipapillata have opened the way for the molecular analysis of an ancient nervous system, which includes stinging cells, an unusual neurosensory and neurosecretory cell type. They hold some surprises for the mechanisms and evolution of sensory transduction that could not have been anticipated from what has been learned from flies and vertebrates. Research in BMC Biology now implicates the ancient opsin-mediated transduction pathway in the neuronal control of stinging cell discharge.
See research article http://0-www.biomedcentral.com.brum.beds.ac.uk/1741-7007/10/17
- Sensory Neuron
- Spider Silk
- Capsule Wall
- Metazoan Evolution
- Spider Silk Protein
Each nematocyte contains one giant vesicle that is derived from the Golgi apparatus, which is packed with neurotoxic and hemolytic venoms and a coiled spiny tubule inside a capsule, the nematocyst (cnidocyst, cnida) . The 'sting' of a jellyfish shares more similarity with fast neurotransmitter release at a synapse than with the sting of a wasp or stinging nettle, because a nematocyst vesicle unloads its contents (that is, the capsule) by ultra-fast exocytosis . This process is initiated when a prey deflects the ciliary mechanoreceptor, triggering an action potential and the opening of calcium-channels . During the discharge of hydra stenoteles, one of the most elaborated nematocyst types, the barbed part of the tubule is accelerated in less than 700 ns, generating accelerations greater than 5,000,000 g and a pressure of up to 7 GPa, sufficient to penetrate even the cuticles of crustaceans . This ultrafast process is powered by a high osmotic pressure of 150 bars that elastically stretches the capsule wall to which the long and barbed nematocyst tubule is attached. A proteome analysis of the secretome of Hydra magnipapillata  provides molecular clues as to how the elasticity and tensile strength of the capsule wall is achieved, featuring unique structural proteins with elastic properties. Minicollagens constitute a major subgroup of these nematocyst-specific extracellular proteins, but another important constituent, dubbed 'cnidoin' is non-collagenous, resembling the spider silk protein spidroin-2.
The work of Plachetzki and colleagues  now shows that the sensory neuron of the battery complex is a photoreceptor that controls the discharge process. These authors have demonstrated that this sensory neuron co-expresses components of the phototransduction cascade: opsin, a cyclic nucleotide gated (CNG) ion channel, and arrestin. After carrying out behavioral trials with Hydra, Plachetzki and colleagues concluded that different light intensities elicit significant effects on cnidocyte discharge. The readiness of stenoteles to discharge was significantly smaller under bright light conditions than in dim light. Treatment of Hydra with an inhibitor of CNG ion channels (cis-diltiazem) rescued this inhibition.
Photosensitive behavior of Hydra has been observed previously, but this is the first study to provide clear evidence that it can be traced to a cellular receptor. The surprising new findings are that sensory neurons in the battery-cell complex of Hydra tentacles exhibit this photosensitivity and, more importantly, that light information is used to control nematocyte discharge. The authors present several hypotheses that might explain light-regulated nematocyte discharge. Of these hypotheses, one is particularly intriguing as it assumes a further optimization of discharge: a shadow being cast by the prey on a battery complex could enhance the likelihood that stenoteles hit their target .
Nematocytes are the major cell population in a Hydra, and they are maintained by a stem cell system that also gives rise to nerve cells. It is therefore parsimonious to assume that the observed integration of light information by opsin-based signaling into the control of nematocyte discharge is under strong selective pressure. This selective pressure might even have led to the formation of ocelli in hydrozoan medusae (for example, in Podocoryne carnea) or even to the complex lens eyes in box jelly fishes (for example, in Carybdea marsupialis or Tripedalia cystophora).
Thanks to Ildiko Somorjai, Suat Özbek, and Bert Hobmayer for critically reading the manuscript.
- Nüchter T, Benoit M, Engel U, Ozbek S, Holstein TW: Nanosecond-scale kinetics of nematocyst discharge. Curr Biol. 2006, 16: R316-318. 10.1016/j.cub.2006.03.089.PubMedView ArticleGoogle Scholar
- Ozbek S, Balasubramanian PG, Holstein TW: Cnidocyst structure and the biomechanics of discharge. Toxicon. 2009, 54: 1038-1045. 10.1016/j.toxicon.2009.03.006.PubMedView ArticleGoogle Scholar
- Balasubramanian PG, Beckmann A, Warnken U, Schnölzer M, Schüler A, Bornberg-Bauer E, Holstein TW, Özbek S: Proteome of Hydranematocyst. J Biol Chem. 2012, Google Scholar
- Thorington GU, McAuley V, Hessinger DA: Effects of satiation and starvation on nematocyst discharge, prey killing, and ingestion in two species of sea anemone. Biol Bull. 2010, 219: 122-131.PubMedGoogle Scholar
- Mahoney JL, Graugnard EM, Mire P, Watson GM: Evidence for involvement of TRPA1 in the detection of vibrations by hair bundle mechanoreceptors in sea anemones. J Comp Physiol A Neuroethol Sens Neural Behav Physiol. 2011, 197: 729-742. 10.1007/s00359-011-0636-7.PubMedView ArticleGoogle Scholar
- Hobmayer E, Holstein TW, David CN: Tentacle morphogenesis in hydra. II. Formation of a complex between a sensory nerve cell and a battery cell. Development. 1990, 109: 897-904.Google Scholar
- Plachetzki DV, Fong CR, Oakley TH: Cnidocyte discharge is regulated by light and opsin-mediated phototransduction. BMC Biol. 2012, 10: 17-10.1186/1741-7007-10-17.PubMedPubMed CentralView ArticleGoogle Scholar
- Hayakawa E, Fujisawa C, Fujisawa T: Involvement of Hydra achaete-scute gene CnASH in the differentiation pathway of sensory neurons in the tentacles. Dev Genes Evol. 2004, 214: 486-492.PubMedGoogle Scholar
- Hartz AJ, Sherr BF, Sherr EB: Photoresponse in the heterotrophic marine dinoflagellate Oxyrrhis marina. J Eukaryot Microbiol. 2011, 58: 171-177. 10.1111/j.1550-7408.2011.00529.x.PubMedView ArticleGoogle Scholar
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