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Claudin5a is required for proper inflation of Kupffer's vesicle lumen and organ laterality.
Kim, Jeong-Gyun; Bae, Sung-Jin; Lee, Hye Shin; Park, Ji-Hyeon; Kim, Kyu-Won.
Afiliação
  • Kim JG; Department of Molecular Medicine and Biopharmaceutical Science, Graduate School of Convergence Science and Technology, Seoul National University, Seoul, Korea.
  • Bae SJ; SNU-Harvard NeuroVascular Protection Research Center, College of Pharmacy and the Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul, Korea.
  • Lee HS; SNU-Harvard NeuroVascular Protection Research Center, College of Pharmacy and the Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul, Korea.
  • Park JH; SNU-Harvard NeuroVascular Protection Research Center, College of Pharmacy and the Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul, Korea.
  • Kim KW; SNU-Harvard NeuroVascular Protection Research Center, College of Pharmacy and the Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul, Korea.
PLoS One ; 12(8): e0182047, 2017.
Article em En | MEDLINE | ID: mdl-28771527
ABSTRACT
Left-right asymmetric organ development is critical to establish a proper body plan of vertebrates. In zebrafish, the Kupffer's vesicle (KV) is a fluid-filled sac which controls asymmetric organ development, and a properly inflated KV lumen by means of fluid influx is a prerequisite for the asymmetric signal transmission. However, little is known about the components that support the paracellular tightness between the KV luminal epithelial cells to sustain hydrostatic pressure during KV lumen expansion. Here, we identified that the claudin5a (cldn5a) is highly expressed at the apical surface of KV epithelial cells and tightly seals the KV lumen. Downregulation of cldn5a in zebrafish showed a failure in organ laterality that resulted from malformed KV. In addition, accelerated fluid influx into KV by combined treatment of forskolin and 3-isobutyl-1-methylxanthine failed to expand the partially-formed KV lumen in cldn5a morphants. However, malformed KV lumen and defective heart laterality in cldn5a morphants were significantly rescued by exogenous cldn5a mRNA, suggesting that the tightness between the luminal epithelial cells is important for KV lumen formation. Taken together, these findings suggest that cldn5a is required for KV lumen inflation and left-right asymmetric organ development.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peixe-Zebra / Cílios / Padronização Corporal / Proteínas de Peixe-Zebra / Embrião não Mamífero / Claudina-5 / Lateralidade Funcional / Morfogênese Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peixe-Zebra / Cílios / Padronização Corporal / Proteínas de Peixe-Zebra / Embrião não Mamífero / Claudina-5 / Lateralidade Funcional / Morfogênese Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2017 Tipo de documento: Article