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1.
Int J Mol Sci ; 22(20)2021 Oct 15.
Artigo em Inglês | MEDLINE | ID: mdl-34681801

RESUMO

Cytochromes P450 (CYP) are enzymes responsible for the biotransformation of most endogenous and exogenous agents. The expression of each CYP is influenced by a unique combination of mechanisms and factors including genetic polymorphisms, induction by xenobiotics, and regulation by cytokines and hormones. In recent years, Ciona robusta, one of the closest living relatives of vertebrates, has become a model in various fields of biology, in particular for studying inflammatory response. Using an in vivo LPS exposure strategy, next-generation sequencing (NGS) and qRT-PCR combined with bioinformatics and in silico analyses, compared whole pharynx transcripts from naïve and LPS-exposed C. robusta, and we provide the first view of cytochrome genes expression and miRNA regulation in the inflammatory response induced by LPS in a hematopoietic organ. In C. robusta, cytochromes belonging to 2B,2C, 2J, 2U, 4B and 4F subfamilies were deregulated and miRNA network interactions suggest that different conserved and species-specific miRNAs are involved in post-transcriptional regulation of cytochrome genes and that there could be an interplay between specific miRNAs regulating both inflammation and cytochrome molecules in the inflammatory response in C. robusta.


Assuntos
Ciona intestinalis , Sistema Enzimático do Citocromo P-450 , Inflamação/genética , Animais , Ciona intestinalis/efeitos dos fármacos , Ciona intestinalis/genética , Sistema Enzimático do Citocromo P-450/efeitos dos fármacos , Sistema Enzimático do Citocromo P-450/genética , Perfilação da Expressão Gênica , Regulação Enzimológica da Expressão Gênica/efeitos dos fármacos , Sequenciamento de Nucleotídeos em Larga Escala , Inflamação/induzido quimicamente , Inflamação/metabolismo , Inflamação/patologia , Lipopolissacarídeos , Família Multigênica/efeitos dos fármacos , Família Multigênica/genética , Faringe/efeitos dos fármacos , Faringe/metabolismo , Faringe/patologia , Filogenia , Transcriptoma/efeitos dos fármacos
2.
J Exp Zool A Ecol Integr Physiol ; 335(3): 339-347, 2021 03.
Artigo em Inglês | MEDLINE | ID: mdl-33503327

RESUMO

Tris(1-chloro-2-propyl)phosphate (TCPP) is the most common chlorinated organophosphorus flame retardant in seawater. Due to its chemical features and abundance, TCPP has been classified as a high hazard, and restrictions of use have been set in multiple countries. Despite TCPP being highly present in the marine environment, only a few studies have explored the TCPP impact on the development of marine invertebrates. Ascidians are important invertebrate members of benthic marine communities and reliable model systems for ecotoxicological research. The aim of this study was to assess the adverse effects of TCPP exposure on the embryogenesis of the ascidian Ciona intestinalis. Our results showed that this pollutant affected both muscles and nervous system development. Malformations appeared similar to those reported in other animal models for other flame retardants, suggesting that these molecules could share a common mechanism of action and induce a mixture effect when simultaneously present in the aquatic environment even at sub-teratogenic concentrations.


Assuntos
Ciona intestinalis/efeitos dos fármacos , Ciona intestinalis/embriologia , Embrião não Mamífero/efeitos dos fármacos , Retardadores de Chama/toxicidade , Compostos Organofosforados/toxicidade , Animais
3.
Nanotoxicology ; 14(10): 1415-1431, 2020 12.
Artigo em Inglês | MEDLINE | ID: mdl-33186509

RESUMO

Nanoplastics are considered contaminants of emerging concern at the global scale. The recent evidence of their occurrence in seawater from the Mediterranean Sea calls for a thorough evaluation of their impact on marine life and in particular on vulnerable life stages such as planktonic embryos. Here, we investigated the impact of increasing nominal concentrations of 50 nm amino-modified (PS-NH2) and 60 nm carboxy-modified (PS-COOH) polystyrene nanoparticles (PS NPs) on the embryonic development of the ascidian Ciona robusta (phylum Chordata), a common benthic invertebrate living in Mediterranean coastal areas with the peculiarity of being an early chordate developmental model. A strong agglomeration of PS-COOH (approx. 1 µm) was observed in natural sea water (NSW) already at time 0, while PS-NH2 resulted still monodispersed (approx. 130 nm) but largely aggregated after 22 h with a microscale dimension similar to those negatively charged. However, their effect on C. robusta embryos development largely differed at 22 h: PS-COOH did not affect larvae phenotypes nor their development, while PS-NH2 caused a dose-dependent effect (EC50 (22 h) of 7.52 µg mL-1) with various degrees of phenotype malformations (from mild to severe) and impairment of larval swimming. Embryos (up to 30%) exposed to 15 µg mL-1 PS-NH2 resulted not developed and the majority was unable to hatch. Calculated PS-NH2 EC50 resulted higher than those available for other marine invertebrate species, suggesting a protective role of the egg envelopes surrounding C. robusta embryos toward nanoplastics exposure.


Assuntos
Ciona intestinalis/efeitos dos fármacos , Desenvolvimento Embrionário/efeitos dos fármacos , Microplásticos/toxicidade , Nanopartículas/toxicidade , Poliestirenos/toxicidade , Poluentes Químicos da Água/toxicidade , Animais , Ciona intestinalis/crescimento & desenvolvimento , Embrião não Mamífero/efeitos dos fármacos , Larva/efeitos dos fármacos , Água do Mar/química
4.
Artigo em Inglês | MEDLINE | ID: mdl-32093017

RESUMO

Polycyclic aromatic hydrocarbons (PAHs) are pollutants that exert harmful effects on marine invertebrates; however, the molecular mechanism underlying PAH action remains unclear. We investigated the effect of PAHs on the ascidian Ciona intestinalis type A (Ciona robusta). First, the influence of PAHs on early Ciona development was evaluated. PAHs such as dibenzothiophene, fluorene, and phenanthrene resulted in formation of abnormal larvae. PAH treatment of swimming larva induced malformation in the form of tail regression. Additionally, we observed the Cionaaryl hydrocarbon receptor (Ci-AhR) mRNA expression in swimming larva, mid body axis rotation, and early juvenile stages. The time correlation between PAH action and AhR mRNA expression suggested that Ci-AhR could be associated with PAH metabolism. Lastly, we analyzed Ci-AhR mRNA localization in Ciona juveniles. Ci-AhR mRNA was localized in the digestive tract, dorsal tubercle, ganglion, and papillae of the branchial sac, suggesting that Ci-AhR is a candidate for an environmental pollutant sensor and performs a neural function. Our results provide basic knowledge on the biological function of Ci-AhR and PAH activity in marine invertebrates.


Assuntos
Ciona intestinalis/efeitos dos fármacos , Poluentes Ambientais/toxicidade , Hidrocarbonetos Policíclicos Aromáticos/toxicidade , Animais , Larva , Receptores de Hidrocarboneto Arílico
5.
J Exp Zool A Ecol Integr Physiol ; 331(1): 5-16, 2019 01.
Artigo em Inglês | MEDLINE | ID: mdl-30218549

RESUMO

Bisphenol A (BPA) is an organic pollutant derived from plastic degradation that has numerous and variable adverse effects on human health and wildlife. In particular, it has been reported that BPA can alter reproductive processes and nervous system development in vertebrates. Considering BPA presence in marine environment and the scant data available on its interaction with nervous system development, we analyzed the effect of BPA exposure on sperm viability, fertilization, embryogenesis, and neural differentiation of the ascidian Ciona robusta. Ascidians are members of the Phylum Tunicata, the sister group of Vertebrata, sharing with them fundamental developmental processes. Our results showed that first cell division was altered starting from 5 µM concentration. Lethal concentration (LC 50 ) was estimated to be 5.2 µM. Larvae developed from treated embryos showed specific malformations to the pigment cells even at 0.1 µM, corresponding to the highest environmental concentration reported so far. Moreover, GABAergic and dopaminergic neurons proved to be target organs of BPA teratogenic action, in accordance with similar results reported in vertebrate animal models. Overall, our results suggest that BPA can exert its effects on nervous system acting on different pathways and underline that C. robusta is a valuable invertebrate animal model for preliminary screenings of effects of pollutants on vertebrates.


Assuntos
Compostos Benzidrílicos/toxicidade , Ciona intestinalis/efeitos dos fármacos , Ciona intestinalis/embriologia , Neurogênese/efeitos dos fármacos , Fenóis/toxicidade , Poluentes Químicos da Água/toxicidade , Animais , Compostos Benzidrílicos/administração & dosagem , Relação Dose-Resposta a Droga , Embrião não Mamífero/efeitos dos fármacos , Larva/efeitos dos fármacos , Dose Letal Mediana , Masculino , Sistema Nervoso/embriologia , Óvulo , Fenóis/administração & dosagem , Espermatozoides , Poluentes Químicos da Água/administração & dosagem
6.
Int J Food Sci Nutr ; 69(7): 805-813, 2018 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-29336191

RESUMO

Nano-encapsulation is a technology used to pack substances in order to enhance their stability and bioavailability, but this packing may interact with living systems, causing unexpected toxicity. Vitamin A (vit A) is a substance that has received attention, because in developed countries, the increasing availability of supplements is leading to its excessive intake. This study aims to compare teratogenic effects caused by exposure to the traditional formulation of vit A versus nano-encapsulated vit A. We used ascidian embryos as an alternative model. Ascidians are marine organisms closely related to vertebrates that share with them a body plan and developmental programme, including the morphogenetic role of retinoic acid (RA). Our data showed that the adverse effects of exposure to the same concentration of the two formulations were different, suggesting that the nano-encapsulation increased the bioavailability of the molecule, which could be better absorbed and metabolised to RA, the effective teratogenic substance.


Assuntos
Ciona intestinalis/efeitos dos fármacos , Nanoestruturas/toxicidade , Teratogênicos/toxicidade , Vitamina A/toxicidade , Animais , Disponibilidade Biológica , Lipossomos , Nanoestruturas/administração & dosagem , Testes de Toxicidade , Vitamina A/administração & dosagem
7.
Environ Toxicol Pharmacol ; 57: 76-85, 2018 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-29223040

RESUMO

The aim of this work was to evaluate the Ascidian Embryo Teratogenicity assay (AET) as new alternative invertebrate model to test the developmental effects of the co-exposure to ethanol and fluconazole. Ciona intestinalis embryos were exposed to the azolic fungicide fluconazole, (FLUCO, 7.8-250µM), to ethanol (Eth, 0.01-0.5%) and to their mixture (0.01% Eth+FLUCO 7.8-250µM) from neurula to larval stage. At the end of the exposure period, larvae were morphologically evaluated and benchmark analysis performed by using the PROAST modelling software. Both compounds were teratogenic in a concentration-related manner, particularly affecting the pigmented organs. The co-exposure to Eth enhanced the effects of FLUCO, the additive hypothesis was not rejected by the modelling. The results demonstrated that AET could be considered a good vertebrate-free alternative model for toxicological investigation in embryos.


Assuntos
Antifúngicos/toxicidade , Ciona intestinalis/efeitos dos fármacos , Etanol/toxicidade , Fluconazol/toxicidade , Animais , Bioensaio , Ciona intestinalis/embriologia , Interações Medicamentosas , Embrião não Mamífero/anormalidades , Embrião não Mamífero/efeitos dos fármacos , Desenvolvimento Embrionário/efeitos dos fármacos , Membrana dos Otólitos/anormalidades , Membrana dos Otólitos/efeitos dos fármacos , Testes de Toxicidade/métodos
8.
Zygote ; 26(1): 14-23, 2018 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-29233211

RESUMO

In marine animals with external fertilization, gametes are released into seawater where fertilization and embryo development occur. Consequently, pollutants introduced into the marine environment by human activities may affect gametes and embryos. These xenobiotics can alter cell physiology with consequent reduction of fertilization success. Here the adverse effects on the reproductive processes of the marine invertebrate Ciona intestinalis (ascidian) of different xenobiotics: lead, zinc, an organic tin compound and a phenylurea herbicide were evaluated. By using the electrophysiological technique of whole-cell voltage clamping, the effects of these compounds on the mature oocyte plasma membrane electrical properties and the electrical events of fertilization were tested by calculating the concentration that induced 50% normal larval formation (EC50). The results demonstrated that sodium currents in mature oocytes were reduced in a concentration-dependent manner by all tested xenobiotics, with the lowest EC50 value for lead. In contrast, fertilization current frequencies were differently affected by zinc and organic tin compound. Toxicity tests on gametes demonstrated that sperm fertilizing capability and fertilization oocyte competence were not altered by xenobiotics, whereas fertilization was inhibited in zinc solution and underwent a reduction in organic tin compound solution (EC50 value of 1.7 µM). Furthermore, fertilized oocytes resulted in a low percentage of normal larvae with an EC50 value of 0.90 µM. This study shows that reproductive processes of ascidians are highly sensitive to xenobiotics suggesting that they may be considered a reliable biomarker and that ascidians are suitable model organisms to assess marine environmental quality.


Assuntos
Ciona intestinalis/efeitos dos fármacos , Oócitos/efeitos dos fármacos , Oócitos/fisiologia , Poluentes Químicos da Água/toxicidade , Xenobióticos/toxicidade , Animais , Membrana Celular/efeitos dos fármacos , Ciona intestinalis/fisiologia , Diurona/toxicidade , Relação Dose-Resposta a Droga , Eletrofisiologia/métodos , Feminino , Fertilização/efeitos dos fármacos , Larva/efeitos dos fármacos , Chumbo/administração & dosagem , Chumbo/toxicidade , Masculino , Sódio/metabolismo , Interações Espermatozoide-Óvulo/efeitos dos fármacos , Testes de Toxicidade/métodos , Poluentes Químicos da Água/administração & dosagem , Xenobióticos/administração & dosagem , Zinco/administração & dosagem , Zinco/toxicidade
9.
J Toxicol Environ Health A ; 80(16-18): 807-819, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28837417

RESUMO

Anthropogenic pollutants produce oxidative stress in marine organisms, directly or following generation of reactive oxygen species (ROS), potentially resulting in increased accumulation of DNA strand breaks quantified. The aim of this study is to quantify baseline levels of DNA strand breaks in marine species from four phyla and to assess relative sensitivity to oxidative stress as well as ability to recover. DNA strand breaks were determined using a formamidopyrimidine DNA glycosylase (Fpg)-amended comet assay in circulating cells from blue mussel (Mytilus edulis), shore crab (Carcinus maenas), sea star (Asterias rubens), and vase tunicate (Ciona intestinalis). Lymphocytes from Atlantic cod (Gadus morhua) were used as a reference. In addition to immediate analysis, cells from all species were exposed ex vivo to two concentrations of hydrogen peroxide (H2O2) at 25 or 250 µM prior to assay. Mean baseline DNA strand breaks were highest for cells from sea star (34%) followed by crab (25%), mussel (22%), tunicate (17%), and cod (14%). Circulating cells from invertebrates were markedly more sensitive to oxidative stress compared to cod lymphocytes. DNA strand breaks exceeded 80% for sea star, crab, and mussel cells following exposure to the lowest H2O2 concentration. There was no recovery for cells from any species following 1 hr in buffer. This study provides an in-depth analysis of DNA integrity for ecologically important species representing 4 phyla. Data indicate that circulating cells from invertebrates are more sensitive to oxidative stress than cells from fish as evidenced by DNA strand breaks. Future studies need to address the extent to which DNA strand breaks may exert consequences for body maintenance costs in marine invertebrates.


Assuntos
Organismos Aquáticos/efeitos dos fármacos , Dano ao DNA/efeitos dos fármacos , Peróxido de Hidrogênio/toxicidade , Estresse Oxidativo/efeitos dos fármacos , Poluentes Químicos da Água/toxicidade , Animais , Organismos Aquáticos/genética , Asterias/efeitos dos fármacos , Asterias/genética , Braquiúros/efeitos dos fármacos , Braquiúros/genética , Ciona intestinalis/efeitos dos fármacos , Ciona intestinalis/genética , Ensaio Cometa , DNA-Formamidopirimidina Glicosilase/metabolismo , Determinação de Ponto Final , Peixes/genética , Linfócitos/efeitos dos fármacos , Linfócitos/metabolismo , Mytilus edulis/efeitos dos fármacos , Mytilus edulis/genética , Especificidade da Espécie
10.
Gen Comp Endocrinol ; 246: 105-115, 2017 05 15.
Artigo em Inglês | MEDLINE | ID: mdl-27292788

RESUMO

Teneurin C-terminal associated peptide (TCAP) is a neuropeptide that bears some structural similarity to the corticotropin-releasing factor (CRF) family of peptides. TCAP and CRF are both implicated in the regulation of stress-related behaviors, as established in rodent models. However, in vertebrates, both TCAP and CRF possess three additional paralogous forms making vertebrate models difficult to assess with respect to TCAP-CRF interaction. As a urochordate, this species possesses single homologs of TCAP and of a CRF/Diuretic-like peptide (CDLP) in the genome, thereby establishing Ciona intestinalis as an excellent model organism to examine the interaction of these peptide systems. However, the lack of C. intestinalis synthetic peptides and specific antisera has complicated experimentation. We, therefore, prepared synthetic versions of CDLP and TCAP to prepare specific antisera and to investigate their bioactivity in this species. To analyze stress-related behaviors, a novel behavioral assay was used to characterize different types of contraction-based behaviors, using buccal opening contractions, cloacal opening contractions, lateral contractions, longitudinal contractions and expulsions. Protein and mRNA expression data indicate that the mature versions of both peptides are present in a number of tissues. With respect to behavioral activity, both TCAP- and CDLP-treated animals had distinct contraction profiles under ambient conditions. Moreover, food stimulation tests revealed that whereas CDLP-treated animals displayed a strong expulsion behavior in response to feeding, TCAP-treated animals did not show this effect. These actions are consistent with previous studies done in vertebrates.


Assuntos
Comportamento Animal/efeitos dos fármacos , Ciona intestinalis/efeitos dos fármacos , Hormônio Liberador da Corticotropina/farmacologia , Diuréticos/farmacologia , Comportamento Alimentar/efeitos dos fármacos , Fragmentos de Peptídeos/farmacologia , Peptídeos/farmacologia , Animais , Formação de Anticorpos , Western Blotting , Ciona intestinalis/imunologia , Ciona intestinalis/metabolismo , Hormônio Liberador da Corticotropina/genética , Fragmentos de Peptídeos/genética , Fragmentos de Peptídeos/imunologia , Peptídeos/genética , RNA Mensageiro/genética , Coelhos , Reação em Cadeia da Polimerase em Tempo Real , Reação em Cadeia da Polimerase Via Transcriptase Reversa
11.
Nanotoxicology ; 10(8): 1096-104, 2016 10.
Artigo em Inglês | MEDLINE | ID: mdl-27080039

RESUMO

Nickel nanoparticles (Ni NPs) are increasingly used in modern industries as catalysts, sensors, and in electronic applications. Due to this large use, their inputs into marine environment have significantly increased; however, the potential ecotoxicological effects in marine environment have so far received little attention. In particular, little is known on the impact of NPs on gamete quality of marine organisms and on the consequences on fertility potential. The present study examines, for the first time, the impact of Ni NPs exposure on sperm quality of the marine invertebrate Ciona intestinalis (ascidian). Several parameters related with sperm status such as plasma membrane lipid peroxidation, mitochondrial membrane potential (MMP), intracellular pH, DNA integrity, and fertilizing ability were assessed as toxicity end points after exposure to different Ni NPs concentrations. Ni NPs generate oxidative stress that in turn induces lipid peroxidation and DNA fragmentation, and alters MMP and sperm morphology. Furthermore, sperm exposure to Ni NPs affects their fertilizing ability and causes developmental anomalies in the offspring. All together, these results reveal a spermiotoxicity of Ni NPs in ascidians suggesting that the application of these NPs should be carefully assessed as to their potential toxic effects on the health of marine organisms that, in turn, may influence the ecological system. This study shows that ascidian sperm represent a suitable and sensitive tool for the investigation of the toxicity of NPs entered into marine environment, for defining the mechanisms of toxic action and for the environmental monitoring purpose.


Assuntos
Ciona intestinalis/efeitos dos fármacos , Nanopartículas Metálicas/toxicidade , Níquel/toxicidade , Espermatozoides/efeitos dos fármacos , Poluentes Químicos da Água/toxicidade , Animais , Ciona intestinalis/crescimento & desenvolvimento , Ciona intestinalis/metabolismo , Monitoramento Ambiental , Fertilidade/efeitos dos fármacos , Peroxidação de Lipídeos/efeitos dos fármacos , Masculino , Potencial da Membrana Mitocondrial/efeitos dos fármacos , Nanopartículas Metálicas/química , Níquel/química , Estresse Oxidativo/efeitos dos fármacos , Espermatozoides/metabolismo , Espermatozoides/patologia , Poluentes Químicos da Água/química
12.
Proteomics ; 15(23-24): 4064-79, 2015 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-26223815

RESUMO

Sperm proteins mediating sperm-egg interaction should be exhibited on the sperm surface, or exposed or released when sperm approach an egg. In ascidians (protochordates), sperm undergo a sperm reaction, characterized by enhanced sperm motility and mitochondrial swelling and shedding on contact with the vitelline coat (VC) or by treatment with Ca(2+) ionophore. Here, proteomic analysis was conducted on sperm exudates and sperm surface proteins using ionomycin-induced sperm reaction and cell-impermeable labeling in Ciona intestinalis type A (C. robusta). In the exudate from sperm treated with ionomycin, membrane proteins including a possible VC receptor CiUrabin were abundant, indicating the release of membranous compartments during sperm reaction. Among the surface proteins XP_009859314.1 (uncharacterized protein exhibiting homology to HrTTSP-1) was most abundant before the sperm reaction, but XP_004227079.1 (unknown Ig superfamily protein) appears to be most abundantly exposed by the sperm reaction. Moreover, proteins containing a notable set of domains, astacin-like metalloprotease domain and thrombospondin type 1 repeat(s), were found in this fraction. Possible roles in fertilization as well as localizations and behaviors of these proteins are discussed.


Assuntos
Ciona intestinalis/metabolismo , Ionomicina/farmacologia , Proteômica , Espermatozoides/metabolismo , Animais , Ionóforos de Cálcio/farmacologia , Ciona intestinalis/efeitos dos fármacos , Masculino , Complexo de Endopeptidases do Proteassoma/metabolismo , Espermatozoides/efeitos dos fármacos , Ubiquitina/metabolismo
13.
Biochem Biophys Res Commun ; 463(4): 656-60, 2015 Aug 07.
Artigo em Inglês | MEDLINE | ID: mdl-26043689

RESUMO

In vivo toxicity evaluation using model organisms is an important step for the development of new drugs. Here, we report that Ciona intestinalis, a chordate invertebrate, is beneficial to drug toxicity evaluation for the following reasons: rapid embryonic and larval development, resemblance to vertebrates, ease of management, low cost, transparent body, and low risk of ethical issues. The dynamic phenotypic change of Ciona larvae during metamorphosis prompted us to examine the effect of cytotoxic drugs on its development by quantifying six toxicity endpoints: degenerated tail size, ampulla length, rotation of body axis, stomach size, heart rate, and body size. As a result, mitochondrial respiratory inhibitors, tubulin polymerization/depolymerization inhibitors, or DNA/RNA synthesis inhibitors showed distinct toxicity profiles against these six endpoints, but drugs with the same targets showed a similar toxicity profile in Ciona. Our results suggest Ciona is an effective animal model for profiling drug toxicity and exploring the mechanisms of drugs with unknown targets.


Assuntos
Ciona intestinalis/efeitos dos fármacos , Testes de Toxicidade/métodos , Animais , Antineoplásicos/toxicidade , Análise por Conglomerados
14.
Elife ; 4: e05361, 2015 Apr 13.
Artigo em Inglês | MEDLINE | ID: mdl-25866928

RESUMO

The Ciona notochord displays planar cell polarity (PCP), with anterior localization of Prickle (Pk) and Strabismus (Stbm). We report that a myosin is polarized anteriorly in these cells and strongly colocalizes with Stbm. Disruption of the actin/myosin machinery with cytochalasin or blebbistatin disrupts polarization of Pk and Stbm, but not of myosin complexes, suggesting a PCP-independent aspect of myosin localization. Wash out of cytochalasin restored Pk polarization, but not if done in the presence of blebbistatin, suggesting an active role for myosin in core PCP protein localization. On the other hand, in the pk mutant line, aimless, myosin polarization is disrupted in approximately one third of the cells, indicating a reciprocal action of core PCP signaling on myosin localization. Our results indicate a complex relationship between the actomyosin cytoskeleton and core PCP components in which myosin is not simply a downstream target of PCP signaling, but also required for PCP protein localization.


Assuntos
Ciona intestinalis/citologia , Regulação da Expressão Gênica no Desenvolvimento , Miosinas/genética , Notocorda/citologia , Citoesqueleto de Actina/efeitos dos fármacos , Citoesqueleto de Actina/genética , Citoesqueleto de Actina/metabolismo , Animais , Proteínas de Bactérias/genética , Proteínas de Bactérias/metabolismo , Núcleo Celular/efeitos dos fármacos , Núcleo Celular/metabolismo , Núcleo Celular/ultraestrutura , Polaridade Celular/efeitos dos fármacos , Ciona intestinalis/efeitos dos fármacos , Ciona intestinalis/embriologia , Ciona intestinalis/metabolismo , Citocalasina B/farmacologia , Embrião não Mamífero , Proteínas Fetais/genética , Proteínas Fetais/metabolismo , Expressão Gênica , Compostos Heterocíclicos de 4 ou mais Anéis/farmacologia , Proteínas Luminescentes/genética , Proteínas Luminescentes/metabolismo , Miosinas/metabolismo , Notocorda/efeitos dos fármacos , Notocorda/embriologia , Notocorda/metabolismo , Isoformas de Proteínas/genética , Isoformas de Proteínas/metabolismo , Proteínas Recombinantes de Fusão/genética , Proteínas Recombinantes de Fusão/metabolismo , Transdução de Sinais , Proteínas com Domínio T/genética , Proteínas com Domínio T/metabolismo , Fatores ras de Troca de Nucleotídeo Guanina/genética , Fatores ras de Troca de Nucleotídeo Guanina/metabolismo
15.
Open Biol ; 5(3): 140182, 2015 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-25788553

RESUMO

Polyunsaturated aldehydes (PUAs) are fatty-acid-derived metabolites produced by some microalgae, including different diatom species. PUAs are mainly produced as a wound-activated defence mechanism against microalgal predators or released from senescent cells at the end of a bloom. PUAs, including 2,4-trans-decadienal (DD), induce deleterious effects on embryonic and larval development of several planktonic and benthic organisms. Here, we report on the effects of DD on larval development and metamorphosis of the ascidian Ciona intestinalis. Ciona larval development is regulated by the cross-talking of different molecular events, including nitric oxide (NO) production, ERK activation and caspase 3-dependent apoptosis. We report that treatment with DD at the competence larval stage results in a delay in metamorphosis. DD affects redox balance by reducing total glutathione and NO levels. By biochemical and quantitative gene expression analysis, we identify the NO-signalling network affected by DD, including the upregulation of ERK phosphatase mkp1 and consequent reduction of ERK phosphorylation, with final changes in the expression of downstream ERK target genes. Overall, these results give new insights into the molecular pathways induced in marine organisms after exposure to PUAs during larval development, demonstrating that this aldehyde affects key checkpoints of larval transition from the vegetative to the reproductive life stage.


Assuntos
Aldeídos/farmacologia , Ciona intestinalis/efeitos dos fármacos , Ciona intestinalis/fisiologia , Diatomáceas/química , MAP Quinases Reguladas por Sinal Extracelular/metabolismo , Estágios do Ciclo de Vida/efeitos dos fármacos , Óxido Nítrico/metabolismo , Transdução de Sinais/efeitos dos fármacos , Animais , Regulação da Expressão Gênica/efeitos dos fármacos , Homeostase/efeitos dos fármacos , Metamorfose Biológica/efeitos dos fármacos , Oxirredução/efeitos dos fármacos , Fosforilação , Fatores de Tempo
16.
Mar Drugs ; 13(3): 1451-65, 2015 Mar 17.
Artigo em Inglês | MEDLINE | ID: mdl-25789602

RESUMO

The anti-proliferative effects of diatoms, described for the first time in copepods, have also been demonstrated in benthic invertebrates such as polychaetes, sea urchins and tunicates. In these organisms PUAs (polyunsaturated aldehydes) induce the disruption of gametogenesis, gamete functionality, fertilization, embryonic mitosis, and larval fitness and competence. These inhibitory effects are due to the PUAs, produced by diatoms in response to physical damage as occurs during copepod grazing. The cell targets of these compounds remain largely unknown. Here we identify some of the genes targeted by the diatom PUA 2-trans-4-trans-decadienal (DD) using the tunicate Ciona intestinalis. The tools, techniques and genomic resources available for Ciona, as well as the suitability of Ciona embryos for medium-to high-throughput strategies, are key to their employment as model organisms in different fields, including the investigation of toxic agents that could interfere with developmental processes. We demonstrate that DD can induce developmental aberrations in Ciona larvae in a dose-dependent manner. Moreover, through a preliminary analysis, DD is shown to affect the expression level of genes involved in stress response and developmental processes.


Assuntos
Aldeídos/farmacologia , Ciona intestinalis/efeitos dos fármacos , Diatomáceas/química , Genes Controladores do Desenvolvimento/efeitos dos fármacos , Aldeídos/administração & dosagem , Aldeídos/isolamento & purificação , Animais , Ciona intestinalis/genética , Relação Dose-Resposta a Droga , Ensaios de Triagem em Larga Escala , Larva/efeitos dos fármacos , Estresse Fisiológico/efeitos dos fármacos
17.
J Invertebr Pathol ; 126: 6-11, 2015 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-25659264

RESUMO

We investigated the role of phenoloxidases (POs) in ascidians inflammatory reaction, a components of a copper-containing protein family involved in invertebrate immune system. In Ciona intestinalis two phenoloxidases (CinPO-1, CinPO-2) have been sequenced. In the present study, real time PCR analysis showed that both CinPO-1 and CinPO-2 genes were modulated by LPS inoculation suggesting that they are inducible and highly expressed in the inflamed pharynx. In situ hybridization disclosed CinPO-1 and CinPO-2 transcripts in pharynx hemocytes (granulocytes) and, mainly, in unilocular refractile granulocytes (URG) which mainly populated the inflamed tunic matrix. Interestingly, the genes are also upregulated by LPS in the endostyle (zones 7, 8 and 9) that is considered homolog to the vertebrate thyroid.


Assuntos
Ciona intestinalis/enzimologia , Lipopolissacarídeos/farmacologia , Monofenol Mono-Oxigenase/metabolismo , Animais , Ciona intestinalis/efeitos dos fármacos , Ciona intestinalis/imunologia , Hemócitos/efeitos dos fármacos , Hemócitos/enzimologia , Hemócitos/imunologia , Hibridização In Situ , Monofenol Mono-Oxigenase/genética , Reação em Cadeia da Polimerase em Tempo Real , Regulação para Cima/efeitos dos fármacos
18.
PLoS One ; 9(7): e102907, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25058405

RESUMO

In the ascidian Ciona intestinalis larval development and metamorphosis require a complex interplay of events, including nitric oxide (NO) production, MAP kinases (ERK, JNK) and caspase-3 activation. We have previously shown that NO levels affect the rate of metamorphosis, regulate caspase activity and promote an oxidative stress pathway, resulting in protein nitration. Here, we report that NO down-regulates MAP kinase phosphatases (mkps) expression affecting positively ERK signaling. By pharmacological approach, we observed that the reduction of endogenous NO levels caused a decrease of ERK phosphorylation, whereas increasing levels of NO induced ERK activation. We have also identified the ERK gene network affected by NO, including mpk1, mpk3 and some key developmental genes by quantitative gene expression analysis. We demonstrate that NO induces an ERK-independent down-regulation of mkp1 and mkp3, responsible for maintaining the ERK phosphorylation levels necessary for transcription of key metamorphic genes, such as the hormone receptor rev-erb and the van willebrand protein vwa1c. These results add new insights into the role played by NO during larval development and metamorphosis in Ciona, highlighting the cross-talk between different signaling pathways.


Assuntos
Ciona intestinalis/genética , Regulação da Expressão Gênica no Desenvolvimento , Metamorfose Biológica/genética , Fosfatases da Proteína Quinase Ativada por Mitógeno/genética , Óxido Nítrico/metabolismo , Transdução de Sinais/efeitos dos fármacos , Sequência de Aminoácidos , Animais , Caspase 3/genética , Caspase 3/metabolismo , Ciona intestinalis/efeitos dos fármacos , Ciona intestinalis/crescimento & desenvolvimento , Ciona intestinalis/metabolismo , MAP Quinases Reguladas por Sinal Extracelular/genética , MAP Quinases Reguladas por Sinal Extracelular/metabolismo , Perfilação da Expressão Gênica , Larva/efeitos dos fármacos , Larva/genética , Larva/crescimento & desenvolvimento , Larva/metabolismo , MAP Quinase Quinase 4/genética , MAP Quinase Quinase 4/metabolismo , Fosfatases da Proteína Quinase Ativada por Mitógeno/antagonistas & inibidores , Fosfatases da Proteína Quinase Ativada por Mitógeno/metabolismo , Dados de Sequência Molecular , Óxido Nítrico/farmacologia , Fosforilação , Receptores Citoplasmáticos e Nucleares/genética , Receptores Citoplasmáticos e Nucleares/metabolismo , Alinhamento de Sequência , Transdução de Sinais/genética , Fator de von Willebrand/genética , Fator de von Willebrand/metabolismo
19.
Aquat Toxicol ; 152: 47-56, 2014 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-24727215

RESUMO

The major thiol-containing molecules involved in controlling the level of intracellular ROS in eukaryotes, acting as a nonenzymatic detoxification system, are metallothioneins (MTs), glutathione (GSH) and phytochelatins (PCs). Both MTs and GSH are well-known in the animal kingdom. PC was considered a prerogative of the plant kingdom but, in 2001, a phytochelatin synthase (PCS) gene was described in the nematode Caenorhabditis elegans; additional genes encoding this enzyme were later described in the earthworm Eisenia fetida and in the parasitic nematode Schistosoma mansoni but scanty data are available, up to now, for Deuterostomes. Here, we describe the molecular characteristics and transcription pattern, in the presence of Cd, of a PCS gene from the invertebrate chordate Ciona intestinalis, a ubiquitous solitary tunicate and demonstrate the presence of PCs in tissue extracts. We also studied mRNA localization by in situ hybridization. In addition, we analyzed the behavior of hemocytes and tunic cells consequent to Cd exposure as well as the transcription pattern of the Ciona orthologous for proliferating cell nuclear antigen (PCNA), usually considered a proliferation marker, and observed that cell proliferation occurs after 96h of Cd treatment. This matches the hypothesis of Cd-induced cell proliferation, as already suggested by previous data on the expression of a metallothionein gene in the same animal.


Assuntos
Aminoaciltransferases/genética , Cádmio/toxicidade , Ciona intestinalis/efeitos dos fármacos , Regulação Enzimológica da Expressão Gênica/efeitos dos fármacos , Poluentes Químicos da Água/toxicidade , Sequência de Aminoácidos , Aminoaciltransferases/química , Aminoaciltransferases/metabolismo , Animais , Cádmio/análise , Ciona intestinalis/química , Ciona intestinalis/classificação , Ciona intestinalis/enzimologia , Ciona intestinalis/genética , Perfilação da Expressão Gênica , Ordem dos Genes , Dados de Sequência Molecular , Filogenia , Alinhamento de Sequência , Poluentes Químicos da Água/análise
20.
Cryobiology ; 68(1): 43-9, 2014 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-24269530

RESUMO

In cryopreservation procedures, the capacity to protect the cells from freezing and thawing processes is sensitive to the choice of the cryoprotective agent (CPA) and to its optimal concentration. The advancement of research on Tunicate model species has raised interest in liquid nitrogen cryopreservation for the storage and distribution of genetic resources. Ciona intestinalis (Linnè, 1767) consists of a complex of cryptic taxa that are central to several areas of investigation, from comparative genomics to invasive biology. Here we investigated how five CPAs, three chilling rates and two freezing rates influence semen cryopreservation in C. intestinalis sp. A. By using larval morphology and motility as endpoints, we estimated that long term semen storage requires 10% dimethyl sulfoxide as a protective agent, -1°C/min chilling rate (18°C to 5°C) and -13°C/min freezing rate (5°C to -80°C), followed by immersion in liquid nitrogen.


Assuntos
Ciona intestinalis/efeitos dos fármacos , Criopreservação , Crioprotetores/farmacologia , Dimetil Sulfóxido/farmacologia , Preservação do Sêmen/métodos , Espermatozoides/efeitos dos fármacos , Animais , Ciona intestinalis/citologia , Ciona intestinalis/fisiologia , Conservação dos Recursos Naturais , Feminino , Fertilização in vitro , Congelamento , Larva/crescimento & desenvolvimento , Masculino , Oócitos/citologia , Oócitos/fisiologia , Motilidade dos Espermatozoides/efeitos dos fármacos , Espermatozoides/citologia , Espermatozoides/fisiologia
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