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Arm loss through a separation at a specialized autotomy plane in echinoderms is inextricably linked to regeneration, but the link between these phenomena is poorly explored. We investigated nervous system regeneration post-autotomy in the asteriid seastar Coscinasterias muricata, focusing on the reorganization of the radial nerve cord (RNC) into the ectoneural neuroepithelium and neuropile, and the hyponeural region, using antibodies to the seastar-specific neuropeptide SALMFamide-1 (S1). Parallel changes in the associated haemal and coelomic vessels were also examined. A new arm bud appeared in 3-5 days with regeneration over three weeks. At the nerve stump and in the RNC immediately behind, the haemal sinus/hyponeural coelomic compartments enlarged into a hypertrophied space filled with migratory cells that appear to be involved in wound healing and regeneration. The haemal and coelomic compartments provided a conduit for these cells to gain rapid access to the regeneration site. An increase in the number of glia-like cells indicates the importance of these cells in regeneration. Proximal to the autotomy plane, the original RNC exhibited Wallerian-type degeneration, as seen in disorganized axons and enlarged S1-positive varicosities. The imperative to regrow lost arms quickly is reflected in the efficiency of regeneration from the autotomy plane facilitated by the rapid appearance of progenitor-like migratory cells. In parallel to its specialization for defensive arm detachment, the autotomy plane appears to be adapted to promote regeneration. This highlights the importance of examining autotomy-induced regeneration in seastars as a model system to study nervous system regeneration in deuterostomes and the mechanisms involved with the massive migration of stem-like cells to facilitate rapid recovery.
Ben Khadra,
An integrated view of asteroid regeneration: tissues, cells and molecules.
2017, Pubmed,
Echinobase
Ben Khadra,
An integrated view of asteroid regeneration: tissues, cells and molecules.
2017,
Pubmed
,
Echinobase
Blowes,
Body wall structure in the starfish Asterias rubens.
2017,
Pubmed
,
Echinobase
Bossche,
Epithelial origin of starfish coelomocytes.
1976,
Pubmed
,
Echinobase
Byrne,
Development and distribution of the peptidergic system in larval and adult Patiriella: comparison of sea star bilateral and radial nervous systems.
2002,
Pubmed
,
Echinobase
Cobb,
The significance of the radial nerve cords in asteroids and echinoids.
1970,
Pubmed
,
Echinobase
Elphick,
Distribution and action of SALMFamide neuropeptides in the starfish Asterias rubens.
1995,
Pubmed
,
Echinobase
Elphick,
Evolution of neuropeptide signalling systems.
2018,
Pubmed
Elphick,
Isolation of the neuropeptide SALMFamide-1 from starfish using a new antiserum.
1991,
Pubmed
,
Echinobase
Elphick,
SALMFamide salmagundi: the biology of a neuropeptide family in echinoderms.
2014,
Pubmed
,
Echinobase
Ferrario,
Fundamental aspects of arm repair phase in two echinoderm models.
2018,
Pubmed
,
Echinobase
Ferraz Franco,
Proteolytic events are relevant cellular responses during nervous system regeneration of the starfish Marthasterias glacialis.
2014,
Pubmed
,
Echinobase
Ferretti,
Is there a relationship between adult neurogenesis and neuron generation following injury across evolution?
2011,
Pubmed
Gabre,
The coelomic epithelium transcriptome from a clonal sea star, Coscinasterias muricata.
2015,
Pubmed
,
Echinobase
Glass,
Wallerian degeneration as a window to peripheral neuropathy.
2004,
Pubmed
Gorshkov,
[Ultrastructure of coelomic epithelium and coelomocytes of intact and wounded starfish Asterias rubens L].
2009,
Pubmed
,
Echinobase
Helm,
Early evolution of radial glial cells in Bilateria.
2017,
Pubmed
Hernroth,
Possibility of mixed progenitor cells in sea star arm regeneration.
2010,
Pubmed
,
Echinobase
Holm,
Induced cell proliferation in putative haematopoietic tissues of the sea star, Asterias rubens (L.).
2008,
Pubmed
,
Echinobase
Koenig,
Rapid mobility of motile varicosities and inclusions containing alpha-spectrin, actin, and calmodulin in regenerating axons in vitro.
1985,
Pubmed
Lin,
Pedal peptide/orcokinin-type neuropeptide signaling in a deuterostome: The anatomy and pharmacology of starfish myorelaxant peptide in Asterias rubens.
2017,
Pubmed
,
Echinobase
Malkinson,
Clustering of excess growth resources within leading growth cones underlies the recurrent "deposition" of varicosities along developing neurites.
2010,
Pubmed
Mashanov,
Radial glial cells play a key role in echinoderm neural regeneration.
2013,
Pubmed
,
Echinobase
Mladenov,
Mechanisms of arm-tip regeneration in the sea star, Leptasterias hexactis.
1989,
Pubmed
,
Echinobase
Morrens,
Glial cells in adult neurogenesis.
2012,
Pubmed
Newman,
Tissue distribution of the SALMFamide neuropeptides S1 and S2 in the starfish Asterias rubens using novel monoclonal and polyclonal antibodies. I. Nervous and locomotory systems.
1995,
Pubmed
,
Echinobase
O'Neill,
Structure and mechanics of starfish body wall.
1989,
Pubmed
,
Echinobase
Pinsino,
Coelomocytes and post-traumatic response in the common sea star Asterias rubens.
2007,
Pubmed
,
Echinobase
Thorndyke,
Molecular approach to echinoderm regeneration.
2001,
Pubmed
,
Echinobase
Wilkie,
Autotomy as a prelude to regeneration in echinoderms.
2001,
Pubmed
,
Echinobase
Wu,
Molecular mechanisms of peripheral nerve regeneration: emerging roles of microRNAs.
2013,
Pubmed
Zachary,
A role for neuropeptides in the control of cell proliferation.
1987,
Pubmed