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Molecular mechanism of the suppression of larval skeleton by polycyclic aromatic hydrocarbons in early development of sea urchin <Emphasis Type="Italic">Hemicentrotus pulcherrimus</Emphasis>
Authors:Toshio Sekiguchi  Koji Yachiguchi  Masato Kiyomoto  Shouzo Ogiso  Shuichi Wada  Yoshiaki Tabuchi  Chun-Sang Hong  Ajai K Srivastav  Stephen D J Archer  Stephen B Pointing  Kazuichi Hayakawa  Nobuo Suzuki
Institution:1.Noto Marine Laboratory, Institute of Nature and Environmental Technology,Kanazawa University,Housu-gun,Japan;2.Marine and Coastal Research Center,Ochanomizu University,Tateyama,Japan;3.Department of Animal Bioscience, Faculty of Bioscience,Nagahama Institute of Bio-Science and Technology,Nagahama,Japan;4.Division of Molecular Genetics Research, Life Science Research Center,University of Toyama,Toyama,Japan;5.Research and Business Foundation, Hankuk University of Foreign Studies,Yongin-si,Republic of Korea;6.Department of Zoology,D.D.U. Gorakhpur University,Gorakhpur,India;7.Institute for Applied Ecology New Zealand,Auckland University of Technology,Auckland,New Zealand;8.Yale-NUS College,National University of Singapore,Singapore,Singapore;9.Institute of Nature and Environmental Technology,Kanazawa University,Kanazawa,Japan
Abstract:Polycyclic aromatic hydrocarbons including benza]anthracene (BaA) are priority pollutants in the aquatic environment. Our previous study revealed that BaA and its metabolite, 4-monohydroxylated BaA (4-OHBaA) inhibit larval skeletogenesis in the sea urchin Hemicentrotus pulcherrimus. Here we report studies to elucidate the target of skeletogenesis inhibition elicited by BaA and 4-OHBaA. First, we performed an in vitro experiment using isolated micromeres which give rise to the larval skeletogenic mesenchyme. However, skeletogenesis was not repressed by BaA and 4-OHBaA, implying that these chemicals indirectly influence on the formation of larval skeleton. Next, we analyzed their influence in vivo using embryos. Vascular endothelial growth factor (VEGF) that is expressed in the ectoderm and induces spicule formation was inhibited by BaA and 4-OHBaA treatment. These chemicals also suppressed the expression of the heparan sulfate 6-O endosulfatase (Sulf) known as a VEGF signaling modulator. We, therefore, propose that BaA and 4-OHBaA effects on larval skeletogenesis via VEGF signaling. Furthermore, we showed that the expression of Endo16 mRNA, an endodermal marker, decreased after BaA and 4-OHBaA exposure, suggesting that these chemicals affect endodermal function together with skeletogenesis. This study demonstrates that BaA and 4-OHBaA exert multiple detrimental effects on the development of H. pulcherrimus.
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