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Normal development of preimplantation mouse embryos deficient in gap junctional coupling

Normal development of preimplantation mouse embryos deficient in gap junctional coupling
Normal development of preimplantation mouse embryos deficient in gap junctional coupling
The connexin multigene family (13 characterized members in rodents) encodes the subunits of gap junction channels. Gap junctional intercellular coupling, established during compaction of the preimplantation mouse embryo, is assumed to be necessary for development of the blastocyst. One member of the connexin family, connexin43, has been shown to contribute to the gap junctions that form during compaction, yet embryos homozygous for a connexin43 null mutation develop normally, at least until implantation. We show that this can be explained by contributions from one or more additional connexin genes that are normally expressed along with connexin43 in preimplantation development. Immunogold electron microscopy confirmed that roughly 30% of gap junctions in compacted morulae contain little or no connexin43 and therefore are likely to be composed of another connexin(s). Confocal immunofluorescence microscopy was then used to demonstrate that connexin45 is also assembled into membrane plaques, beginning at the time of compaction. Correspondingly, embryos homozygous for the connexin43 null mutation were found to retain the capacity for cell-to-cell transfer of fluorescent dye (dye coupling), but at a severely reduced level and with altered permeability characteristics. Whereas mutant morulae showed no evidence of dye coupling when tested with 6-carboxyfluorescein, dye coupling could be demonstrated using 2′,7′-dichlorofluorescein, revealing permeability characteristics previously established for connexin45 channels. We conclude that preimplantation development in the mouse can proceed normally even though both the extent and nature of gap junctional coupling have been perturbed. Despite the distinctive properties of connexin43 channels, their role in preimplantation development can be fulfilled by one or more other types of gap junction channels.
0021-9533
1751-1758
De Sousa, P.A.
5c50018a-a94d-42a8-b229-51537523884c
Juneja, S.C.
69c47c96-23fb-4dd2-b30d-b098817f7869
Caveney, S.
ea15ed70-f2cb-4aa1-a15d-27aae4a3cf2b
Houghton, F.D.
53946041-127e-45a8-9edb-bf4b3c23005f
Davies, T.C.
f083b483-7180-4bca-8b52-4be2b669e09e
Reaume, A.G.
fff8581f-69c7-4036-832c-13ec1757e239
Rossant, J.
949ff5e2-5108-4eb6-8b3d-efc70d49921c
Kidder, G.M.
d6babdf4-43cc-4806-b0d0-d0c02088c4d9
De Sousa, P.A.
5c50018a-a94d-42a8-b229-51537523884c
Juneja, S.C.
69c47c96-23fb-4dd2-b30d-b098817f7869
Caveney, S.
ea15ed70-f2cb-4aa1-a15d-27aae4a3cf2b
Houghton, F.D.
53946041-127e-45a8-9edb-bf4b3c23005f
Davies, T.C.
f083b483-7180-4bca-8b52-4be2b669e09e
Reaume, A.G.
fff8581f-69c7-4036-832c-13ec1757e239
Rossant, J.
949ff5e2-5108-4eb6-8b3d-efc70d49921c
Kidder, G.M.
d6babdf4-43cc-4806-b0d0-d0c02088c4d9

De Sousa, P.A., Juneja, S.C., Caveney, S., Houghton, F.D., Davies, T.C., Reaume, A.G., Rossant, J. and Kidder, G.M. (1997) Normal development of preimplantation mouse embryos deficient in gap junctional coupling. Journal of Cell Science, 110 (15), 1751-1758. (doi:10.1242/jcs.110.15.1751).

Record type: Article

Abstract

The connexin multigene family (13 characterized members in rodents) encodes the subunits of gap junction channels. Gap junctional intercellular coupling, established during compaction of the preimplantation mouse embryo, is assumed to be necessary for development of the blastocyst. One member of the connexin family, connexin43, has been shown to contribute to the gap junctions that form during compaction, yet embryos homozygous for a connexin43 null mutation develop normally, at least until implantation. We show that this can be explained by contributions from one or more additional connexin genes that are normally expressed along with connexin43 in preimplantation development. Immunogold electron microscopy confirmed that roughly 30% of gap junctions in compacted morulae contain little or no connexin43 and therefore are likely to be composed of another connexin(s). Confocal immunofluorescence microscopy was then used to demonstrate that connexin45 is also assembled into membrane plaques, beginning at the time of compaction. Correspondingly, embryos homozygous for the connexin43 null mutation were found to retain the capacity for cell-to-cell transfer of fluorescent dye (dye coupling), but at a severely reduced level and with altered permeability characteristics. Whereas mutant morulae showed no evidence of dye coupling when tested with 6-carboxyfluorescein, dye coupling could be demonstrated using 2′,7′-dichlorofluorescein, revealing permeability characteristics previously established for connexin45 channels. We conclude that preimplantation development in the mouse can proceed normally even though both the extent and nature of gap junctional coupling have been perturbed. Despite the distinctive properties of connexin43 channels, their role in preimplantation development can be fulfilled by one or more other types of gap junction channels.

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Published date: 1 August 1997
Additional Information: © 1997 by Company of Biologists

Identifiers

Local EPrints ID: 457876
URI: http://eprints.soton.ac.uk/id/eprint/457876
ISSN: 0021-9533
PURE UUID: 56716e58-701c-4ade-9c99-e884b7a419af
ORCID for F.D. Houghton: ORCID iD orcid.org/0000-0002-5167-1694

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Date deposited: 21 Jun 2022 18:08
Last modified: 17 Mar 2024 03:05

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Contributors

Author: P.A. De Sousa
Author: S.C. Juneja
Author: S. Caveney
Author: F.D. Houghton ORCID iD
Author: T.C. Davies
Author: A.G. Reaume
Author: J. Rossant
Author: G.M. Kidder

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