A sea urchin Na+K+2Cl− cotransporter is involved in the maintenance of calcification-relevant cytoplasmic cords in Strongylocentrotus droebachiensis larvae
Basse, Wiebke C., Gutowska, Magdalena A., Findeisen, Ulrike, Stumpp, Meike, Dupont, Sam, Jackson, Daniel J., Himmerkus, Nina, Melzner, Frank and Bleich, Markus (2015) A sea urchin Na+K+2Cl− cotransporter is involved in the maintenance of calcification-relevant cytoplasmic cords in Strongylocentrotus droebachiensis larvae Comparative Biochemistry and Physiology A - Molecular and Integrative Physiology, 187 . pp. 184-192. DOI 10.1016/j.cbpa.2015.05.005.
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The cellular mechanisms of calcification in sea urchin larvae are still not well understood. Primary mesenchyme cells within the larval body cavity form a syncytium to secrete CaCO3 spicules from intracellular amorphous CaCO3 (ACC) stores. We studied the role of Na+K+2Cl− cotransporter (NKCC) in intracellular ACC accumulation and larval spicule formation of Strongylocentrotus droebachiensis. First, we incubated growing larvae with three different loop diuretics (azosemide, bumetanide, and furosemide) and established concentration-response curves. All loop diuretics were able to inhibit calcification already at concentrations that specifically inhibit NKCC. Calcification was most effectively inhibited by azosemide (IC50 = 6.5 μM), while larval mortality and swimming ability were not negatively impacted by the treatment. The inhibition by bumetanide (IC50 = 26.4 μM) and furosemide (IC50 = 315.4 μM) resembled the pharmacological fingerprint of the mammalian NKCC1 isoform. We further examined the effect of azosemide on the maintenance of cytoplasmic cords and on the occurrence of calcification vesicles using fluorescent dyes (calcein, FM1-43). Fifty micromolars of azosemide inhibited the maintenance of cytoplasmic cords and resulted in increased calcein fluorescence within calcification vesicles. The expression of NKCC in S. droebachiensis was verified by PCR and Western blot with a specific NKCC antibody. In summary, the pharmacological profile of loop diuretics and their specific effects on calcification in sea urchin larvae suggest that they act by inhibition of NKCC via repression of cytoplasmic cord formation and maintenance.
|Keywords:||Calcein, Calcification, Loop diuretics, Ion transport, NKCC (Na+K+2Cl− cotransporter), Strongylocentrotus droebachiensis|
|Research affiliation:||Kiel University > Faculty of Medicine > Institute of Physiology
OceanRep > The Future Ocean - Cluster of Excellence > FO-R08
Kiel University > Kiel Marine Science
OceanRep > The Future Ocean - Cluster of Excellence > FO-R04
OceanRep > The Future Ocean - Cluster of Excellence
OceanRep > GEOMAR > FB3 Marine Ecology > FB3-EOE-B Experimental Ecology - Benthic Ecology
|Date Deposited:||13 Jul 2015 11:39|
|Last Modified:||08 Mar 2017 09:56|
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