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Published in: Reproductive Biology and Endocrinology 1/2004

Open Access 01-12-2004 | Research

Expression of connexins in human preimplantation embryos in vitro

Authors: Debra J Bloor, Yvonne Wilson, Mark Kibschull, Otto Traub, Henry J Leese, Elke Winterhager, Susan J Kimber

Published in: Reproductive Biology and Endocrinology | Issue 1/2004

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Abstract

Intercellular communication via gap junctions is required to coordinate developmental processes in the mammalian embryo. We have investigated if the connexin (Cx) isoforms known to form gap junctions in rodent preimplantation embryos are also expressed in human embryos, with the aim of identifying species differences in communication patterns in early development. Using a combination of polyA PCR and immunocytochemistry we have assessed the expression of Cx26, Cx31, Cx32, Cx40, Cx43 and Cx45 which are thought to be important in early rodent embryos. The results demonstrate that Cx31 and Cx43 are the main connexin isoforms expressed in human preimplantation embryos and that these isoforms are co-expressed in the blastocyst. Cx45 protein is expressed in the blastocyst but the protein may be translated from a generally low level of transcripts: which could only be detected in the PN to 4-cell embryos. Interestingly, Cx40, which is expressed by the extravillous trophoblast in the early human placenta, was not found to be expressed in the blastocyst trophectoderm from which this tissue develops. All of the connexin isoforms in human preimplantation embryos are also found in rodents pointing to a common regulation of these connexins in development of rodent and human early embryos and perhaps other species.
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Metadata
Title
Expression of connexins in human preimplantation embryos in vitro
Authors
Debra J Bloor
Yvonne Wilson
Mark Kibschull
Otto Traub
Henry J Leese
Elke Winterhager
Susan J Kimber
Publication date
01-12-2004
Publisher
BioMed Central
Published in
Reproductive Biology and Endocrinology / Issue 1/2004
Electronic ISSN: 1477-7827
DOI
https://doi.org/10.1186/1477-7827-2-25

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