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PMID: 1662598 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Spatiotemporal expression of three gap junction gene products involved in fetomaternal communication during rat pregnancy.

Development (Cambridge, England) ·Vol. 113 ·No. 1 ·1991-09-00 ·Pages 165-81

Risek B, Gilula NB

Abstract

The expression of three different members of the gap junction multigene family, alpha 1 (Cx43), beta 1 (Cx32), and beta 2 (Cx26), was analysed in the rat implantation chamber (a structural unit containing fetal, extraembryonic and maternal components within the pregnant uterus) during mid- and late stages of gestation as well as in the delivering, post-partum and non-pregnant uterus. A differential, spatiotemporal and cell-type-specific regulation of gap junctional coexpression was observed for beta 1 and beta 2 in all epithelia examined (visceral, luminal and glandular), as well as for alpha 1 and beta 2 in decidual cells and keratinocytes of the fetal epidermis. alpha 1 antigen was detected in the mesometrial stroma, mesometrial myometrium, connective tissue, mesothelia of the amnion and visceral yolk sac and in the allantoic mesodermal layer throughout gestation. In addition, expression of alpha 1 in the placental basal zone and trophoblast giant cells coincided with the differentiation of these cells. beta 2 expression was observed prominently in the chorionic villi of the placental labyrinth. The presence of beta 1 and beta 2 in the visceral epithelium (visceral yolk sac = the primary route for embryonic nourishment prior to the formation of the chorioallantoic placenta) and beta 2 in the chorionic villi (placental barrier = the major fetomaternal exchange route) suggests that gap junctions have an important role in fetomaternal communication.

MeSH Terms
Animals Cell Communication/genetics Connexins Embryo, Mammalian/ultrastructure Female Gene Expression Regulation/physiology Gestational Age Immunohistochemistry Intercellular Junctions/physiology Membrane Proteins/genetics Pregnancy Pregnancy, Animal/genetics Rats Rats, Inbred Strains Uterus/ultrastructure
Chemicals
Connexins Membrane Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Risek B
Department of Molecular Biology, Research Institute of Scripps Clinic, La Jolla, CA 92037.
Gilula N B
Article Info
Journal
Development (Cambridge, England)
Abbr.
Development
ISSN
0950-1991
Published
1991-09-00
Pages
165-81
Language
English
Region
England
NLM ID
8701744
Subset
IM
Grants
NIGMS NIH HHS · GM 37904 · United States
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