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The involvement of Eph-Ephrin signaling in tissue separation and convergence during Xenopus gastrulation movements SCIE SCOPUS

Title
The involvement of Eph-Ephrin signaling in tissue separation and convergence during Xenopus gastrulation movements
Authors
Park, ECCho, GSKim, GHChoi, SCHan, JK
Date Issued
2011-02-15
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Abstract
In Xenopus gastrulation, the involuting mesodermal and non-involuting ectodermal cells remain separated from each other, undergoing convergent extension. Here, we show that Eph-ephrin signaling is crucial for the tissue separation and convergence during gastrulation. The loss of EphA4 function results in aberrant gastrulation movements, which are due to selective inhibition of tissue constriction and separation. At the cellular levels, knockdown of EphA4 impairs polarization and migratory activity of gastrulating cells but not specification of their fates. Importantly, rescue experiments demonstrate that EphA4 controls tissue separation via RhoA GTPase in parallel to Fz7 and PAPC signaling. In addition, we show that EphA4 and its putative ligand, ephrin-A1 are expressed in a complementary manner in the involuting mesodermal and non-involuting ectodermal layers of early gastrulae, respectively. Depletion of ephrin-A1 also abrogates tissue separation behaviors. Therefore, these results suggest that Eph receptor and its ephrin ligand might mediate repulsive interaction for tissue separation and convergence during early Xenopus gastrulation movements. (C) 2010 Elsevier Inc. All rights reserved.
Keywords
EphA4; Ephrin-A1; Tissue separation; CE movements; Gastrulation; Brachet' s cleft; Xenopus; RECEPTOR TYROSINE KINASE; CELL POLARITY; PARAXIAL PROTOCADHERIN; MESODERM MIGRATION; LAEVIS EMBRYOS; NEURAL CREST; EXPRESSION; ADHESION; EXTENSION; MORPHOGENESIS
URI
https://oasis.postech.ac.kr/handle/2014.oak/25038
DOI
10.1016/J.YDBIO.2010.12.012
ISSN
0012-1606
Article Type
Article
Citation
DEVELOPMENTAL BIOLOGY, vol. 350, no. 2, page. 441 - 450, 2011-02-15
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한진관HAN, JIN KWAN
Dept of Life Sciences
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