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Cnidocyte

Stinging cell used by cnidarians

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Through Cell (biology), Organelle and Toxin

Structure and function

Each cnidocyte contains an organelle called a cnidocyst, which consists of a bulb-shaped capsule and a hollow, coiled tubule that is contained within. Immature cnidocytes are referred to as cnidoblasts or nematoblasts. The externally oriented side of the cell has a hair-like trigger called a cnidocil, a mechano-chemical receptor. When the trigger is activated, the tubule shaft of the cnidocyst is ejected and, in the case of the penetrant nematocyst, the forcefully ejected tubule penetrates the target organism. This discharge takes a few microseconds, and is able to reach accelerations of about 40,000 g. Research from 2006 suggests the process occurs in as little as 700 nanoseconds, thus reaching an acceleration of up to 5,410,000 g. After penetration, the toxic content of the nematocyst is injected into the target organism, allowing the sessile cnidarian to capture the immobilized prey. Recently, in two sea anemone species (Nematostella vectensis and Anthopleura elegantissima), the type I neurotoxin protein Nv1 was shown to be localized in ectodermal gland cells in the tentacles, next to but not in nematocysts. Upon encounter with a crustacean prey, nematocysts discharge and pierce the prey, and Nv1 is massively secreted into the extracellular medium by the nearby gland cells, thus suggesting another mode of entry for toxins.

Cnidocyte capsule composition

The cnidocyte capsule is made of novel Cnidaria-specific gene products which combine known protein domains. Minicollagen gene products (proteins) are one of the major structural components of the capsule. They are very short genes containing the characteristic collagen-triple helix sequence, as well as polyproline domains and cysteine-rich domains. Trimeres of mini collagen proteins assemble through their terminal cysteine-rich domain, forming highly organized and rigid supra-structures. Minicollagen 1 Ncol-1 polymers assemble on the inner shell while the outer capsule is composed of polymerized NOWA (Nematocyst Outer Wall Antigen) proteins. Nemato Galectin, minicollagen Ncol-15 and chondroitin are novel proteins used to build the tubule shaft. In piercing cnidocytes, the novel protein spinalin is used to make the spines present at the base of the shaft.

Discharge mechanism

The cnidocyst capsule stores a large concentration of calcium ions, which are released from the capsule into the cytoplasm of the cnidocyte when the trigger is activated. This causes a large concentration gradient of calcium across the cnidocyte plasma membrane. The resulting osmotic pressure causes a rapid influx of water into the cell. This increase in water volume in the cytoplasm forces the coiled cnidae tubule to eject rapidly. Prior to discharge the coiled cnidae tubule exists inside the cell in an "inside out" condition. The back pressure resulting from the influx of water into the cnidocyte together with the opening of the capsule tip structure or operculum, triggers the forceful eversion of the cnidae tubule causing it to right itself as it comes rushing out of the cell with enough force to impale a prey organism.

That force is to be calculated as the mass of the mechanism's stylet multiplied by its acceleration. The pressure that is generated by this impact into its prey is to be calculated by the stylet's force divided by its area. Researchers have calculated an ejected mass of 1 nanogram, an acceleration of 5,410,000 g and a stylet tip radius of 15 ± 8 nm. Therefore, a pressure of more than 7 GPa was estimated at the stylet tip which they write is in the range of technical bullets.

Fluid dynamics in nematocyst discharge

Few papers have modeled the discharge aside from direct observation. Observational studies typically used a tentacle solution assay with a chemical stimulant to create discharge and cameras to record them. One in 1984 and another in 2006 as imaging technology improved. One study involved computational fluid dynamics where variables such as barb plate size, prey cylindrical diameter and fluid medium Reynolds number were manipulated.

Observational studies indicate that velocities of the barb/stylet decrease throughout the discharge. As such, the incredible maximum acceleration is achieved at the beginning. Dynamic traits such as maximum discharge velocities and trajectory patterns may not correspond to static traits such as tubule lengths and capsule volumes. Therefore, caution is appropriate when using medusan nematocyst assemblages as indicators of prey selection and trophic role. This is possibly the case for other jelly species and hence one cannot generally infer nematocyst static traits to prey size.

Prey detection

Cnidae are "single use" cells, and thus represent a large expenditure of energy to produce. In Hydrozoans, in order to regulate discharge, cnidocytes are connected as "batteries", containing several types of cnidocytes connected to supporting cells and neurons. The supporting cells contain chemosensors, which, together with the mechanoreceptor on the cnidocyte (cnidocil), allow only the right combination of stimuli to cause discharge, such as prey swimming, and chemicals found in prey cuticle or cutaneous tissue. This prevents the cnidarian from stinging itself although sloughed off cnidae can be induced to fire independently.

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