» Articles » PMID: 17623636

Stichopin-containing Nerves and Secretory Cells Specific to Connective Tissues of the Sea Cucumber

Overview
Journal Proc Biol Sci
Specialty Biology
Date 2007 Jul 12
PMID 17623636
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Stichopin, a 17-amino acid peptide isolated from a sea cucumber, affects the stiffness change of the body-wall catch connective tissues and the contraction of the body-wall muscles. The localization of stichopin in sea cucumbers was studied by indirect immunohistochemistry using antiserum against stichopin. Double staining was performed with both stichopin antiserum and 1E11, the monoclonal antibody specific to echinoderm nerves. A stichopin-like immunoreactivity (stichopin-LI) was exclusively found in the connective tissues of various organs. Many fibres and cells with processes were stained by both the anti-stichopin antibody and 1E11. They were found in the body-wall dermis and the connective tissue layer of the cloacae and were suggested to be connective tissue-specific nerves. Oval cells with stichopin-LI (OCS) without processes were found in the body-wall dermis, the connective tissue sheath of the longitudinal body-wall muscles, the connective tissue layer of the tube feet and tentacles, and the connective tissue in the radial nerves separating the ectoneural part from the hyponeural part. Electron microscopic observations of the OCSs in the radial nerves showed that they were secretory cells. The OCSs were located either near the well-defined neural structures or near the water-filled cavities, such as the epineural sinus and the canals of the tube feet. The location near the water-filled cavities might suggest that stichopin was secreted into these cavities to function as a hormone.

Citing Articles

Neuropeptide precursors and neuropeptides in the sea cucumber Apostichopus japonicus: a genomic, transcriptomic and proteomic analysis.

Chen M, Talarovicova A, Zheng Y, Storey K, Elphick M Sci Rep. 2019; 9(1):8829.

PMID: 31222106 PMC: 6586643. DOI: 10.1038/s41598-019-45271-3.


Functional Morphology of the Arm Spine Joint and Adjacent Structures of the Brittlestar Ophiocomina nigra (Echinodermata: Ophiuroidea).

Wilkie I PLoS One. 2016; 11(12):e0167533.

PMID: 27974856 PMC: 5156572. DOI: 10.1371/journal.pone.0167533.


The protein precursors of peptides that affect the mechanics of connective tissue and/or muscle in the echinoderm Apostichopus japonicus.

Elphick M PLoS One. 2012; 7(8):e44492.

PMID: 22952987 PMC: 3432112. DOI: 10.1371/journal.pone.0044492.


Neuroanatomy of the tube feet and tentacles in Holothuria glaberrima (Holothuroidea, Echinodermata).

Diaz-Balzac C, Abreu-Arbelo J, Garcia-Arraras J Zoomorphology. 2010; 129(1):33-43.

PMID: 20461218 PMC: 2866052. DOI: 10.1007/s00435-009-0098-4.

References
1.
Winther A, Muren J, Ahlborg N, Nassel D . Differential distribution of isoforms of Leucophaea tachykinin-related peptides (LemTRPs) in endocrine cells and neuronal processes of the cockroach midgut. J Comp Neurol. 1999; 406(1):15-28. View

2.
Gut A, Kiraly C, Fukuda M, Mikoshiba K, Wollheim C, LANG J . Expression and localisation of synaptotagmin isoforms in endocrine beta-cells: their function in insulin exocytosis. J Cell Sci. 2001; 114(Pt 9):1709-16. DOI: 10.1242/jcs.114.9.1709. View

3.
Sudhof T . Synaptotagmins: why so many?. J Biol Chem. 2001; 277(10):7629-32. DOI: 10.1074/jbc.R100052200. View

4.
Nakajima Y, Humphreys T, Kaneko H, Tagawa K . Development and neural organization of the tornaria larva of the Hawaiian hemichordate, Ptychodera flava. Zoolog Sci. 2004; 21(1):69-78. DOI: 10.2108/0289-0003(2004)21[69:DANOOT]2.0.CO;2. View

5.
Nakajima Y, Kaneko H, Murray G, Burke R . Divergent patterns of neural development in larval echinoids and asteroids. Evol Dev. 2004; 6(2):95-104. DOI: 10.1111/j.1525-142x.2004.04011.x. View