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Differentiation of the epithelial apical junctional complex during mouse preimplantation development: a role for rab13 in the early maturation of the tight junction

Differentiation of the epithelial apical junctional complex during mouse preimplantation development: a role for rab13 in the early maturation of the tight junction
Differentiation of the epithelial apical junctional complex during mouse preimplantation development: a role for rab13 in the early maturation of the tight junction
We have investigated the mechanisms by which the epithelial apicolateral junctional complex (AJC) is generated during trophectoderm differentiation in the mouse blastocyst using molecular, structural and functional analyses. The mature AJC comprises an apical tight junction (TJ), responsible for intercellular sealing and blastocoel formation, and subjacent zonula adherens E-cadherin/catenin adhesion complex which also extends along lateral membrane contact sites. Dual labelling confocal microscopy revealed that the AJC derived from a single ‘intermediate’ complex formed following embryo compaction at the 8-cell stage in which the TJ-associated peripheral membrane protein, ZO-1?? isoform, was co-localized with both ?- and ?-catenin. However, following assembly of the TJ transmembrane protein, occludin, from the early 32-cell stage when blastocoel formation begins, ZO-1?? and other TJ proteins (ZO-1?+ isoform, occludin, cingulin) co-localized in an apical TJ which was separate from a subjacent E-cadherin/catenin zonula adherens complex. Thin-section electron microscopy confirmed that a single zonula adherens-like junctional complex present at the AJC site following compaction matured into a dual TJ and zonula adherens complex at the blastocyst stage. Embryo incubation in the tracer FITC-dextran 4 kDa showed that a functional TJ seal was established coincident with blastocoel formation. We also found that rab13, a small GTPase previously localized to the TJ, is expressed at all stages of preimplantation development and relocates from the cytoplasm to the site of AJC biogenesis from compaction onwards with rab13 and ZO-1?? co-localizing precisely. Our data indicate that the segregation of the two elements of the AJC occurs late in trophectoderm differentiation and likely has functional importance in blastocyst formation. Moreover, we propose a role for rab13 in the specification of the AJC site and the formation and segregation of the TJ.
epithelial differentiation, blastocyst, trophectoderm, mouse embryo, tight junction, zonula adherens, apical junctional complex, ZO-1, rab13, occludin, cingulin, E-Cadherin, catenin
0925-4773
93-104
Sheth, B.
2ca6ed58-a992-47b7-b3a5-3c5df82aada7
Fontaine, J.J.
2adedc8e-f666-4b37-8069-84d876b8459b
Ponza, E.
eb39810d-f409-41f3-94c7-b710bcb4300d
McCallum, A.
21dfc14b-caf0-4869-a231-7acc4f1507b4
Page, A.
76ebbfb8-4fe3-495c-afff-1f2f34977fee
Citi, S.
680742ee-4d59-4f77-90e9-2e47439c11f4
Louvard, D.
29d57e72-53a8-40cb-9aea-aac72f8c6153
Zahraoui, A.
b8e68379-ece6-4463-a16d-b9ed7d0240ee
Fleming, T.P.
2abf761a-e5a1-4fa7-a2c8-12e32d5d4c03
Sheth, B.
2ca6ed58-a992-47b7-b3a5-3c5df82aada7
Fontaine, J.J.
2adedc8e-f666-4b37-8069-84d876b8459b
Ponza, E.
eb39810d-f409-41f3-94c7-b710bcb4300d
McCallum, A.
21dfc14b-caf0-4869-a231-7acc4f1507b4
Page, A.
76ebbfb8-4fe3-495c-afff-1f2f34977fee
Citi, S.
680742ee-4d59-4f77-90e9-2e47439c11f4
Louvard, D.
29d57e72-53a8-40cb-9aea-aac72f8c6153
Zahraoui, A.
b8e68379-ece6-4463-a16d-b9ed7d0240ee
Fleming, T.P.
2abf761a-e5a1-4fa7-a2c8-12e32d5d4c03

Sheth, B., Fontaine, J.J., Ponza, E., McCallum, A., Page, A., Citi, S., Louvard, D., Zahraoui, A. and Fleming, T.P. (2000) Differentiation of the epithelial apical junctional complex during mouse preimplantation development: a role for rab13 in the early maturation of the tight junction. Mechanisms of Development, 97 (1-2), 93-104. (doi:10.1016/S0925-4773(00)00416-0).

Record type: Article

Abstract

We have investigated the mechanisms by which the epithelial apicolateral junctional complex (AJC) is generated during trophectoderm differentiation in the mouse blastocyst using molecular, structural and functional analyses. The mature AJC comprises an apical tight junction (TJ), responsible for intercellular sealing and blastocoel formation, and subjacent zonula adherens E-cadherin/catenin adhesion complex which also extends along lateral membrane contact sites. Dual labelling confocal microscopy revealed that the AJC derived from a single ‘intermediate’ complex formed following embryo compaction at the 8-cell stage in which the TJ-associated peripheral membrane protein, ZO-1?? isoform, was co-localized with both ?- and ?-catenin. However, following assembly of the TJ transmembrane protein, occludin, from the early 32-cell stage when blastocoel formation begins, ZO-1?? and other TJ proteins (ZO-1?+ isoform, occludin, cingulin) co-localized in an apical TJ which was separate from a subjacent E-cadherin/catenin zonula adherens complex. Thin-section electron microscopy confirmed that a single zonula adherens-like junctional complex present at the AJC site following compaction matured into a dual TJ and zonula adherens complex at the blastocyst stage. Embryo incubation in the tracer FITC-dextran 4 kDa showed that a functional TJ seal was established coincident with blastocoel formation. We also found that rab13, a small GTPase previously localized to the TJ, is expressed at all stages of preimplantation development and relocates from the cytoplasm to the site of AJC biogenesis from compaction onwards with rab13 and ZO-1?? co-localizing precisely. Our data indicate that the segregation of the two elements of the AJC occurs late in trophectoderm differentiation and likely has functional importance in blastocyst formation. Moreover, we propose a role for rab13 in the specification of the AJC site and the formation and segregation of the TJ.

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More information

Published date: 16 October 2000
Keywords: epithelial differentiation, blastocyst, trophectoderm, mouse embryo, tight junction, zonula adherens, apical junctional complex, ZO-1, rab13, occludin, cingulin, E-Cadherin, catenin

Identifiers

Local EPrints ID: 56726
URI: http://eprints.soton.ac.uk/id/eprint/56726
ISSN: 0925-4773
PURE UUID: d2d547aa-8452-48a7-83f0-f6d901a6de8a

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Date deposited: 22 Aug 2008
Last modified: 15 Mar 2024 11:03

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Contributors

Author: B. Sheth
Author: J.J. Fontaine
Author: E. Ponza
Author: A. McCallum
Author: A. Page
Author: S. Citi
Author: D. Louvard
Author: A. Zahraoui
Author: T.P. Fleming

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