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Bolstad, K.

Publications and source records attributed to Bolstad, K..

3 recordsLinked to original sources

Novel cell and tissue dynamics drive the unusual biology of the catch tentacle, an inducible organ of aggression found in the sea anemone Metridium senile

Metridium senile is a clonal anemone that engages in fighting interactions to defend its territory from non-clonemates utilizing an inducible fighting organ, the catch tentacle. Upon contact with a non-clonemate, the catch tentacle tip detaches onto the non-clonal individual, resulting in necrosis where the tip attaches to the non-clone. The incapacitating function of the catch tentacle is driven by a unique type of cnidocyte, the holotrich, which is not found elsewhere in M. senile, including the feeding tentacles from which catch tentacles develop. Metridium farcimen, the sister species to M. senile, never develops catch tentacles despite their close phylogenetic relationship, as exemplified by their ability to hybridize. Here, we compare the feeding tentacles of both species to the catch tentacles in M. senile to determine how catch tentacles achieve their unusual function. We found that the feeding tentacles of M. senile and M. farcimen house similar types of cnidocytes that develop from proliferative cells distributed throughout the tentacle. By contrast, catch tentacles house distinct cnidocyte types from feeding tentacles and restrict proliferative cells to the base of the tentacle. This suggests immature cnidocytes migrate from base to tip to replace lost cells after an aggressive interaction in the catch tentacle. Additionally, we observed two morphologically and chemically distinct types of holotrichs in the catch tentacles that appear to use different cues to induce firing. Together, our data suggests that the novelty of catch tentacle aggression is mediated by distinct cell and tissue dynamics.

evolutionary biology↗

Morphological and functional characterization of the ptychocyte, a stingless stinging cell

Cnidocytes (stinging cells), unique to cnidarians (corals, anemones, jellyfish), have diversified into distinct types with variable forms and functions. Nematocytes, cnidocytes found in all cnidarians, are used for prey capture and defense. When triggered, a pressurized capsule inside the nematocyte releases a harpoon-like structure attached to a hollow tubule that pierces prey and delivers venom. Ptychocytes, a cnidocyte unique to tube anemones (sister to corals and sea anemones) discharge a long spineless tubule used exclusively to build the tube in which the animal lives. Given that nematocytes and ptychocytes are specialized for different functions, we hypothesized that they might respond to firing cues in different ways. To test this, we examined the morphology, function, and distribution of nematocytes and ptychocytes in the North American Tube Anemone, Ceriantheopsis americana. We determined that ptychocytes have apical sensory structures like the cones previously described on nematocytes. Surprisingly, the body wall has a dense population of multiciliated cells that appear to function in tube formation. To determine how divergent selection pressures may have affected firing dynamics, we compared the discharge kinematics of cnidocytes from C. americana and the model sea anemone, Nematostella vectensis. Both nematocytes and ptychocytes from C. americana fired slower than nematocytes from N. vectensis, suggesting the rapid discharge speed of sea anemone nematocytes resulted from modification to these cells after sea anemones and tube anemones diverged from their common ancestor. By comparing the morphology and function of different cnidocytes, we can reconstruct the steps that gave rise to cnidocyte diversity.

evolutionary biology↗

Regression of juvenile tentacles is driven by loss of cell proliferation in Haliclystus sanjuanensis, a cnidarian with limited metamorphosis

Medusozoan cnidarians (e.g., jellyfish) metamorphose from a benthic juvenile polyp into a pelagic adult medusa, providing a well-known example of a clade that uses tissue remodeling to create distinct juvenile and adult body plans. Staurozoans (i.e., stalked jellyfish) are an atypical lineage of medusozoans that have lost their medusa stage; thus, their juvenile and adult body plans look remarkably alike. Their limited metamorphosis is characterized by the regression of primary (juvenile) tentacles and the development of secondary (adult) tentacles. In some staurozoan lineages, metamorphosis also involves development of novel adhesive structures (anchors), which are built on top of the regressing primary tentacles. Understanding how cells are partitioned from making juvenile tissues to making adult tissues is important for understanding how animals can make adult structures in the absence of complete metamorphosis. We compared the abundance and distribution of proliferative cells in tissues undergoing regression (primary tentacles) and development (secondary tentacles and anchors) during the juvenile to adult transition in the San Juan Island stalked jellyfish, Haliclystus sanjuanensis. We show that proliferative cells are lost in regressing primary tentacles but are gained in anchors, consistent with a shift in investment from juvenile to adult tissue. Prior to regression, primary and secondary tentacles show similar patterns in their proliferative cell distribution and in the identity of their cnidocytes (stinging cells), indicating that adult tentacles are made by re-deploying a juvenile tentacle program. Finally, we demonstrate that unlike secondary tentacles, primary tentacles cannot regenerate, illustrating that the temporary investment in this tissue is tied to their loss of proliferative cells. Thus, we propose that continued investment in a population of proliferating cells is an important mechanism for segregating temporary tissues (primary tentacles) from long-term tissues (secondary tentacles). These observations of cell dynamics in H. sanjuanensis suggest that temporary investment into juvenile structures may be used to pattern novel adult tissues, providing an important mechanism for diversifying adult body plans.

evolutionary biology↗