IMIS

Publications | Institutes | Persons | Datasets | Projects | Maps
[ report an error in this record ]basket (0): add | show Print this page

Screening of second messengers involved in photocyte bioluminescence control of three ophiuroid species (Ophiuroidea: Echinodermata)
Vanderlinden, C.; Dewael, Y.; Mallefet, J. (2003). Screening of second messengers involved in photocyte bioluminescence control of three ophiuroid species (Ophiuroidea: Echinodermata). J. Exp. Biol. 206(17): 3007-3014. dx.doi.org/10.1242/jeb.00520
In: The Journal of Experimental Biology. Cambridge University Press: London. ISSN 0022-0949; e-ISSN 1477-9145, more
Peer reviewed article  

Available in  Authors 

Keywords
    Amphiura filiformis (O.F. Müller, 1776) [WoRMS]; Echinodermata [WoRMS]; Ophiopsila aranea Forbes, 1843 [WoRMS]; Ophiopsila californica A.H. Clark, 1921 [WoRMS]; Ophiuroidea [WoRMS]
    Marine/Coastal
Author keywords
    invertebrate; echinoderm; ophiuroid; Amphiura filiformis; Ophiopsilaaranea; Ophiopsila californica; bioluminescence; second messenger; cAMP;nervous system; photocyte

Authors  Top 
  • Vanderlinden, C.
  • Dewael, Y.
  • Mallefet, J., more

Abstract
    We investigated the effects of cyclic nucleotides (cGMP and cAMP) and inositol triphosphate/diacylglycerol pathways on the KCl-induced luminescence control of the ophiuroid species Amphiura filiformis, Ophiopsila aranea and Ophiopsila californica. Results show that dibutyrylcGMP, the cGMP analogue, and sodium nitroprusside, the guanylyl cyclase activator, had no effect on the luminescence of O. aranea and O. californica. On the other hand, cGMP could be involved in an inhibitory control in A. filiformis. Dibutyryl-cAMP, the cAMP analogue, and forskolin, the adenylyl cyclase activator, had no effect on maximal light emission, but the adenylyl cyclase inhibitors MDL-12,330A and SQ22,536 affected the kinetics of light production in both Ophiopsila species and strongly reduced KCl-induced luminescence in A. filiformis and O. aranea, suggesting cAMP pathway involvement in photogenesis. The phospholipase C inhibitor U-73122 also strongly reduced KCl-induced luminescence in all three species but this effect seems to be unspecific since U-73343, the inactive analogue of U-73122, equally inhibited photogenesis. Therefore, the results suggest that luminescence control of A. filiformis, O. aranea and O. californica is mediated by cAMP in synergy with calcium.

All data in the Integrated Marine Information System (IMIS) is subject to the VLIZ privacy policy Top | Authors