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dc.contributor.authorTingaud-Sequeira, Angèle-
dc.contributor.authorZapater, Cinta-
dc.contributor.authorChauvigné, François-
dc.contributor.authorOtero, David-
dc.contributor.authorCerdà, Joan-
dc.date.accessioned2010-02-25T11:31:54Z-
dc.date.available2010-02-25T11:31:54Z-
dc.date.issued2009-04-
dc.identifier.citationAmerican Journal Physiology Regulation Integrative and Comparative Physiology 296(4): R1041–R1052 (2009)en_US
dc.identifier.issn0363-6119-
dc.identifier.urihttp://hdl.handle.net/10261/21618-
dc.description13 pages, 7 figures, 3 tablesen_US
dc.description.abstractEmbryos of the marine killifish Fundulus heteroclitus are adapted to survive aerially. However, it is unknown if they are able to control development under dehydration conditions. Here, we show that air-exposed blastula embryos under saturated relative humidity were able to stimulate development, and hence the time of hatching was advanced with respect to embryos continuously immersed in seawater. Embryos exposed to air at later developmental stages did not hatch until water was added, while development was not arrested. Air-exposed embryos avoided dehydration probably because of their thickened egg envelope, although it suffered significant evaporative water loss. The potential role of aquaporins as part of the embryo response to dehydration was investigated by cloning the aquaporin-0 (FhAqp0), -1a (FhAqp1a), and -3 (FhAqp3) cDNAs. Functional expression in Xenopus laevis oocytes showed that FhaAqp1a was a water-selective channel, whereas FhAqp3 was permeable to water, glycerol, and urea. Expression of fhaqp0 and fhaqp1a was prominent during organogenesis, and their mRNA levels were similar between water- and air-incubated embryos. However, fhaqp3 transcripts were highly and transiently accumulated during gastrulation, and the protein product was localized in the basolateral membrane of the enveloping epithelial cell layer and in the membrane of ingressing and migrating blastomers. Interestingly, both fhaqp3 transcripts and FhAqp3 polypeptides were downregulated in air-exposed embryos. These data demonstrate that killifish embryos respond adaptively to environmental desiccation by accelerating development and that embryos are able to transduce dehydration conditions into molecular responses. The reduced synthesis of FhAqp3 may be one of these mechanisms to regulate water and/or solute transport in the embryo.en_US
dc.description.sponsorshipThis study was supported by the European Commission New and Emerging Science and Technologies (NEST) program (contract no. 012674-2 Sleeping Beauty) and by a grant from the Spanish Ministry of Education and Science (MEC; AGL2004-00316/ACU) to J. Cerda`. Participation of C. Zapater and F. Chauvigne´ was financed by a predoctoral fellowship from MEC (Spain) and by the European Commission [Marie Curie Research Training Network Aqua (glycero)porins, MRTN-CT-2006-035995], respectively.en_US
dc.format.extent22195 bytes-
dc.format.mimetypeapplication/pdf-
dc.language.isoengen_US
dc.publisherAmerican Physiological Societyen_US
dc.rightsclosedAccessen_US
dc.subjectFishen_US
dc.subjectDesiccationen_US
dc.subjectHatchingen_US
dc.subjectEgg envelopeen_US
dc.subjectGastrulationen_US
dc.subjectAquaporin-0en_US
dc.subjectAquaporin-1en_US
dc.subjectAquaporin-3en_US
dc.titleAdaptive plasticity of killifish (Fundulus heteroclitus) embryos: dehydration-stimulated development and differential aquaporin-3 expressionen_US
dc.typeartículoen_US
dc.identifier.doi10.1152/ajpregu.91002.2008-
dc.description.peerreviewedPeer revieweden_US
dc.relation.publisherversionhttp://dx.doi.org/10.1152/ajpregu.91002.2008en_US
dc.identifier.e-issn1522-1490-
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