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Dissecting the holothurian nervous system with antibody probes
Author(s) -
DíazBalzac Carlos Antonio,
MiguelRuiz José Enrique San,
Tossas Karen,
RivesSánchez Marisela,
GarcíaArrarás José Enrique
Publication year - 2007
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.21.5.a602-c
Subject(s) - nervous system , echinoderm , neuroanatomy , biology , neuroscience , peripheral nervous system , central nervous system , enteric nervous system , anatomy , ecology
The echinoderm nervous system is one of the least studied of the metazoans. The main focus of previous studies has been the ectoneural and hyponeural components of the nervous system that lie within the nerve ring and radial nerves. Our group has presently identified a nervous plexi located within the connective tissue, which lie outside of the two traditional subdivisions. Its description was made using the monoclonal antibody, RN1, which appears to label the nervous system component of holothurians. In the present work we have used RN1, together with other known markers of nervous elements, such as neuropeptides and neuron‐specific tubulins, to describe different components of the nervous system. Double labeling experiments show that fibers and cells can be grouped into various subpopulations according to the expression of the neural markers, suggesting a larger complexity in the echinoderm nervous system than previously thought. The divisions delineate anatomical circuits of echinoderm neuroanatomy that possibly correlate with particular functions. They also show the connection and possible interactions between the individual components. This description of the echinoderm nervous system, a key group in the evolutionary scale of the deuterostomes, provides important information for comparative neurobiology and evolutionary studies that can enhance the understanding of the nervous system. This work was supported by NSF (IBN‐0110692) and NIH‐MBRS (S06GM08102). CADB and JESR were funded by the UPR‐RP MARC Program (2T34FM07821). We also acknowledge partial support from NIH‐RCMI (RRO‐3641‐01) and the University of Puerto Rico.