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PLoS One
2011 Jan 01;610:e25980. doi: 10.1371/journal.pone.0025980.
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Nitric oxide mediates the stress response induced by diatom aldehydes in the sea urchin Paracentrotus lividus.
Romano G
,
Costantini M
,
Buttino I
,
Ianora A
,
Palumbo A
.
Abstract
Diatoms are ubiquitous and abundant primary producers that have been traditionally considered as a beneficial food source for grazers and for the transfer of carbon through marine food webs. However, many diatom species produce polyunsaturated aldehydes that disrupt development in the offspring of grazers that feed on these unicellular algae. Here we provide evidence that production of the physiological messenger nitric oxide increases after treatment with the polyunsaturated aldehyde decadienal in embryos of the sea urchin Paracentrotus lividus. At high decadienal concentrations, nitric oxide mediates initial apoptotic events leading to loss of mitochondrial functionality through the generation of peroxynitrite. At low decadienal concentrations, nitric oxide contributes to the activation of hsp70 gene expression thereby protecting embryos against the toxic effects of this aldehyde. When nitric oxide levels were lowered by inhibiting nitric oxide synthase activity, the expression of hsp70 in swimming blastula decreased and the proportion of abnormal plutei increased. However, in later pluteus stages nitric oxide was no longer able to exert this protective function: hsp70 and nitric oxide synthase expression decreased with a consequent increase in the expression of caspase-8. Our findings that nitric oxide production increases rapidly in response to a toxic exogenous stimulus opens new perspectives on the possible role of this gas as an important messenger to environmental stress in sea urchins and for understanding the cellular mechanisms underlying toxicity during diatom blooms.
Figure 1. Detection of endogenous NO levels in sea urchin fertilized eggs.NO was revealed by the NOâspecific indicator DAF-FM-DA. (A) Control eggs, (B,C and D) eggs treated for 10 min with 1, 2.5 and 5 µg/ml DD, respectively, and then fertilized. The images were acquired 20 min post-fertilization. (E) Relative fluorescence after 20 min post-fertilization for the same samples reported in the upper panel. White bars indicate relative fluorescence inside the eggs. Gray bars indicate fluorescence in the perivitelline space and fertilization membrane. Values are reported as mean ± S.D. *, p<0.05; *** p<0.001 with respect to the control. Statistical significance of 5 µg/ml: *** p<0.001 compared with 2.5 µg/ml. Control: Nâ=â5; DD 1 µg/ml: Nâ=â4; DD 2.5 µg/ml: Nâ=â4; DD 5 µg/ml: Nâ=â6.
Figure 2. Mitocondrial functionality of developing sea urchin embryos.(A,C and E) Active mitochondria revealed by the mitochondrial-specific fluorescent dye Mitotracker after 50 min post-fertilization. (B,D and F) Corresponding bright field images. (A) Control embryos. (C) Embryos incubated with 5 µg/ml DD; (E) embryos incubated with 5 µg/ml DD in the presence of the peroxynitrite scavenger MnTBAP (10 µM).
Figure 3. Effect of DD on the appearance of blebbing.Sea urchin embryos were treated with DD at different concentrations in the absence or presence of 800 µM c-PTIO as described in materials and method section. Left panel: embryos were monitored for blebbing appearance at 30, 60, 100, 130, 160 and 270 min after fertilization. Control (circle); DD 5 µg/ml (diamond), 2.5 µg/ml (square), 1 µg/ml (triangle), 0.5 µg/ml (star). Dashed lines with empty shapes indicate data obtained in the presence of c-PTIO. Right panel: Control and embryos treated with DD 1 µg/ml in the absence or presence of 800 µM c-PTIO observed at 270 min after fertilization. Values are reported as mean ± S.D.
Figure 4. NO involvement in DD-induced teratogenesis.Embryo development was monitored after 48 hours post fertilization (hpf). (A) Control eggs and eggs treated with TRIM at 20, 50 and 100 µM. (B, C) Eggs treated with DD at 0.1 µg/ml and 0.25 µg/ml, respectively in the absence and presence of TRIM at different concentrations. *** p<0.001 compared to the corresponding DD concentration. Blue: normal plutei. Pink: abnormal plutei.
Figure 5. Gene expression levels using Real Time qPCR.(A) hsp70, NOS and caspase-8 gene expression levels were followed by Real Time qPCR. Samples incubated with DD were collected at 5, 9, 24 and 48 hpf. (B) hsp70 in samples incubated with DD in the absence and presence of TRIM. 5T, 9T, 24T: samples treated with TRIM and collected at 5, 9 and 24 hpf, respectively. 5T+D, 9T+D, 24T+D: samples treated with TRIM and DD and collected at different times. (C) hsp70 in samples incubated with increasing concentrations of sper/NO. Spermine was used as a control. 5INE, 9INE, 24INE: samples treated with spermine at different times; 5NO5, 9NO5, 24NO5: samples treated with sper/NO 5 µM; 5NO10, 9NO10, 24NO10: samples treated with sper/NO 10 µM; 5NO20, 9NO20, 24NO20: samples treated with sper/NO 20 µM; 5NO40, 9NO40, 24NO40: samples treated with sper/NO 40 µM. Data in histograms are expressed as a fold difference from control and are reported as mean ± S.D. Fold differences greater than ±2 (see dotted horizontal guidelines at values of 2 and â2 on the histograms) were considered significant.
Andreou,
Biosynthesis of oxylipins in non-mammals.
2009, Pubmed
Andreou,
Biosynthesis of oxylipins in non-mammals.
2009,
Pubmed
Bishop,
Development of nitric oxide synthase-defined neurons in the sea urchin larval ciliary band and evidence for a chemosensory function during metamorphosis.
2007,
Pubmed
,
Echinobase
Bishop,
NO/cGMP signaling and HSP90 activity represses metamorphosis in the sea urchin Lytechinus pictus.
2001,
Pubmed
,
Echinobase
Bonaventura,
Stress response gene activation protects sea urchin embryos exposed to X-rays.
2011,
Pubmed
,
Echinobase
Bouchard,
Heat stress stimulates nitric oxide production in Symbiodinium microadriaticum: a possible linkage between nitric oxide and the coral bleaching phenomenon.
2008,
Pubmed
Brown,
Inflammatory neurodegeneration mediated by nitric oxide, glutamate, and mitochondria.
2003,
Pubmed
Caldwell,
Inhibition of embryonic development and fertilization in broadcast spawning marine invertebrates by water soluble diatom extracts and the diatom toxin 2-trans,4-trans decadienal.
2002,
Pubmed
,
Echinobase
Caldwell,
The influence of bioactive oxylipins from marine diatoms on invertebrate reproduction and development.
2009,
Pubmed
Casano,
Hsp40 is involved in cilia regeneration in sea urchin embryos.
2003,
Pubmed
,
Echinobase
Cole,
Two ParaHox genes, SpLox and SpCdx, interact to partition the posterior endoderm in the formation of a functional gut.
2009,
Pubmed
,
Echinobase
Cutignano,
Chloroplastic glycolipids fuel aldehyde biosynthesis in the marine diatom Thalassiosira rotula.
2006,
Pubmed
Davidson,
A genomic regulatory network for development.
2002,
Pubmed
,
Echinobase
d'Ippolito,
The role of complex lipids in the synthesis of bioactive aldehydes of the marine diatom Skeletonema costatum.
2004,
Pubmed
Ettensohn,
Gene regulatory networks and developmental plasticity in the early sea urchin embryo: alternative deployment of the skeletogenic gene regulatory network.
2007,
Pubmed
,
Echinobase
Fontana,
LOX-induced lipid peroxidation mechanism responsible for the detrimental effect of marine diatoms on zooplankton grazers.
2007,
Pubmed
Giovine,
Heat stress-activated, calcium-dependent nitric oxide synthase in sponges.
2001,
Pubmed
Giudice,
Studies on heat shock proteins in sea urchin development.
1999,
Pubmed
,
Echinobase
Hansen,
The alpha, beta, gamma, delta-unsaturated aldehyde 2-trans-4-trans-decadienal disturbs DNA replication and mitotic events in early sea urchin embryos.
2004,
Pubmed
,
Echinobase
Ianora,
Toxigenic effects of diatoms on grazers, phytoplankton and other microbes: a review.
2010,
Pubmed
Kröncke,
Inducible nitric oxide synthase-derived nitric oxide in gene regulation, cell death and cell survival.
2001,
Pubmed
Leckie,
The NO pathway acts late during the fertilization response in sea urchin eggs.
2003,
Pubmed
,
Echinobase
Leflaive,
Chemical interactions in diatoms: role of polyunsaturated aldehydes and precursors.
2009,
Pubmed
Malyshev IYu,
Nitric oxide donor induces HSP70 accumulation in the heart and in cultured cells.
1996,
Pubmed
Matranga,
Cellular and biochemical responses to environmental and experimentally induced stress in sea urchin coelomocytes.
2000,
Pubmed
,
Echinobase
Matranga,
Hsp70 as a stress marker of sea urchin coelomocytes in short term cultures.
2002,
Pubmed
,
Echinobase
Mattiello,
Nitric oxide mediates the glutamate-dependent pathway for neurotransmission in Sepia officinalis chromatophore organs.
2010,
Pubmed
Mohri,
Nitric oxide (NO) increase at fertilization in sea urchin eggs upregulates fertilization envelope hardening.
2008,
Pubmed
,
Echinobase
Nemer,
Polyubiquitin RNA characteristics and conditional induction in sea urchin embryos.
1991,
Pubmed
,
Echinobase
Oliveri,
Gene regulatory network controlling embryonic specification in the sea urchin.
2004,
Pubmed
,
Echinobase
Parsell,
The function of heat-shock proteins in stress tolerance: degradation and reactivation of damaged proteins.
1993,
Pubmed
Perez,
Nitric oxide and cnidarian bleaching: an eviction notice mediates breakdown of a symbiosis.
2006,
Pubmed
Pfaffl,
Relative expression software tool (REST) for group-wise comparison and statistical analysis of relative expression results in real-time PCR.
2002,
Pubmed
Pfaffl,
A new mathematical model for relative quantification in real-time RT-PCR.
2001,
Pubmed
Pinsino,
Sea urchin embryos as an in vivo model for the assessment of manganese toxicity: developmental and stress response effects.
2010,
Pubmed
,
Echinobase
Pohnert,
Wound-Activated Chemical Defense in Unicellular Planktonic Algae.
2000,
Pubmed
Ribalet,
Growth inhibition of cultured marine phytoplankton by toxic algal-derived polyunsaturated aldehydes.
2007,
Pubmed
Roccheri,
Synthesis of heat-shock proteins in developing sea urchins.
1981,
Pubmed
,
Echinobase
Roccheri,
Stress proteins by zinc ions in sea urchin embryos.
1988,
Pubmed
,
Echinobase
Roccheri,
Cadmium induces the expression of specific stress proteins in sea urchin embryos.
2004,
Pubmed
,
Echinobase
Roccheri,
Two-dimensional electrophoretic analysis of stress proteins in Paracentrotus lividus.
1993,
Pubmed
,
Echinobase
Roccheri,
EGTA treatment causes the synthesis of heat shock proteins in sea urchin embryos.
2000,
Pubmed
,
Echinobase
Romano,
Teratogenic effects of diatom metabolites on sea urchin Paracentrotus lividus embryos.
2010,
Pubmed
,
Echinobase
Romano,
A marine diatom-derived aldehyde induces apoptosis in copepod and sea urchin embryos.
2003,
Pubmed
,
Echinobase
Rozen,
Primer3 on the WWW for general users and for biologist programmers.
2000,
Pubmed
Sakamaki,
Caspases: evolutionary aspects of their functions in vertebrates.
2009,
Pubmed
Sconzo,
Characterization of a new member of the sea urchin Paracentrotus lividus hsp70 gene family and its expression.
1992,
Pubmed
,
Echinobase
Shi,
Exogenous nitric oxide protect cucumber roots against oxidative stress induced by salt stress.
2007,
Pubmed
Singh,
Nitric oxide alleviates arsenic toxicity by reducing oxidative damage in the roots of Oryza sativa (rice).
2009,
Pubmed
Sluder,
Using sea urchin gametes for the study of mitosis.
1999,
Pubmed
,
Echinobase
Smith,
Neuro-endocrine biomarkers of pollution-induced stress in marine invertebrates.
2000,
Pubmed
Snyder,
Janus faces of nitric oxide.
1993,
Pubmed
Song,
Nitric oxide protects against oxidative stress under heat stress in the calluses from two ecotypes of reed.
2006,
Pubmed
Trapido-Rosenthal,
Increased zooxanthellae nitric oxide synthase activity is associated with coral bleaching.
2005,
Pubmed
Vardi,
A stress surveillance system based on calcium and nitric oxide in marine diatoms.
2006,
Pubmed
Willmott,
Nitric oxide-induced mobilization of intracellular calcium via the cyclic ADP-ribose signaling pathway.
1996,
Pubmed
,
Echinobase
Wu,
Endothelial NOS-deficient mice reveal dual roles for nitric oxide during experimental autoimmune encephalomyelitis.
2009,
Pubmed
Zhang,
Increased abscisic acid levels in transgenic tobacco over-expressing 9 cis-epoxycarotenoid dioxygenase influence H2O2 and NO production and antioxidant defences.
2009,
Pubmed
Zhang,
Detection of nitric oxide in culture media and studies on nitric oxide formation by marine microalgae.
2006,
Pubmed
Zhao,
Nitric oxide protects against polyethylene glycol-induced oxidative damage in two ecotypes of reed suspension cultures.
2008,
Pubmed