Sponge contraction coordination

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Subjects: Molecular and cell biology

Collections: Ecosystems and their environment · Animal signals and responses

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The problem

A freshwater sponge draws water through tiny openings and internal canals. When irritated, it can expand those canals and then squeeze them, flushing material out in a response often called a sneeze. It has no conventional neurons or muscles, yet its many cells take part in an organized movement. Which cells relay the disturbance through the body, and what ends the response?[2] [3]

Scope

The cellular and spatial signalling mechanism that coordinates and terminates the mechanically evoked expansion–contraction cycle in the freshwater demosponge Ephydatia muelleri. Electrical feeding arrest in glass sponges and the evolutionary origin of neurons are separate questions.

What remains open

Researchers know that chemical messages can change the movement. They still need to identify which cells send those messages during a real sneeze, which cells receive them and how one part of the sponge recruits the next. The cells must also know when to stop expanding and begin squeezing.[1] [3]

Why it matters

A filter needs protection from the particles it collects. The sponge provides a concrete example of protective behaviour built from cooperating cells. Explaining the connections would show how sensing water flow can become a coordinated action across an animal, even without the familiar arrangement of nerves sending instructions to muscles.[2] [3]

Research directions

2 directions to explore

Definitions

2 terms
osculum

The opening where water leaves the sponge. Cilia along its lining provide a sensory lead, but the downstream cell-by-cell relay is not established.[3]

P2X-type signalling

Signalling attributed to a class of ATP-responsive receptor channels. Sponge sequences and drug responses suggest involvement, but functional receptors have not been located in particular cells here.[1]

Sources

Partial results
Vanessa R. Ho and colleagues

ATP signalling and its breakdown help separate canal expansion from a complete contraction cycle. Scope: Cultured E. muelleri subjected to glutamate, ATP, ADP, apyrase and the antagonist PPADS.

Bath-applied chemicals do not reproduce native spatial release. Receptor antagonism and predicted sequences do not establish which cells relay the natural wave.

Source date: 2025-02-12ATP caused sustained expansion, whereas ATP with an ATP-degrading enzyme could produce the complete cycle; PPADS blocked responses to ATP and glutamate.Read the source ↗
  1. ATP and glutamate coordinate contractions in the freshwater sponge Ephydatia muelleri Vanessa R. Ho, Greg G. Goss and Sally P. Leys · 2025-02-12
    Notes on ATP and glutamate coordinate contractions in the freshwater sponge Ephydatia muelleri

    Primary full Results, Discussion and proposed Figure 5 pathway read. ATP perturbations support involvement; cell localization and native relay are unresolved.

  2. Evidence for glutamate, GABA and NO in coordinating behaviour in the sponge, Ephydatia muelleri (Demospongiae, Spongillidae) Glen R. D. Elliott and Sally P. Leys
    Notes on Evidence for glutamate, GABA and NO in coordinating behaviour in the sponge, Ephydatia muelleri (Demospongiae, Spongillidae)

    Primary abstract and author PDF Discussion read. Glutamate, inhibition and nitric-oxide localization provide earlier chemical constraints; July 2010 is the issue date.

  3. Evolutionary origins of sensation in metazoans: functional evidence for a new sensory organ in sponges Danielle A. Ludeman and colleagues · 2014-01-13
    Notes on Evolutionary origins of sensation in metazoans: functional evidence for a new sensory organ in sponges

    Full primary abstract and Introduction read. Oscular cilia and reversible loss of response support a flow-sensing structure without identifying its precise molecular sensor.

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