B. Risek et al., GAP JUNCTION REGULATION IN THE UTERUS AND OVARIES OF IMMATURE RATS BYESTROGEN AND PROGESTERONE, Journal of Cell Science, 108, 1995, pp. 1017-1032
The effects of estrogen (E2) and progesterone (P) were examined on the
expression levels of multiple gap junction (GJ) gene products (alpha(
1)=Cx43, beta(1)=Cx32, beta(2)=Cx26) in the uterus and ovaries of imma
ture rats by immunohistochemistry, electron microscopy and northern bl
ot analysis, E2 induced the expression of alpha(1) connexin in the ute
rus (specifically in the myometrium and in endometrial stroma proximal
to luminal epithelium) and ovaries, The E2-induced alpha(1) expressio
n was completely suppressed by P in the uterus, but only partly in ova
ries, Steroid hormones also modulated the quantity, size, and distribu
tion of beta(1) and beta(2) containing junctional plaques along latera
l cell borders in polarized luminal and glandular uterine epithelia. S
mall GJs were detected at basolateral regions in proliferative luminal
epithelium following administration of E2. In contrast, large GJs wer
e localized at subapical-lateral cell borders of the secretory epithel
ium following P-treatment. The co-administration of E2+P had a synergi
stic effect on beta(1) and beta(2) expression in the luminal epitheliu
m, but an inhibitory effect on beta(2) expression in glandular epithel
ium. Myometrial GJs were detected in freeze-fracture replicas as aggre
gates containing regularly arranged particles with particle free zones
, In contrast, GJs in secretory epithelium contained particles which w
ere arranged in a non-crystalline fashion, These GJs contained domains
of mixed and segregated beta(1) and beta(2) antigens within a single
plaque as revealed by laser scanning confocal microscopy analysis of i
mmuno-double-labeled secretory epithelium, The demonstration of segreg
ated antigens within a single GJ plaque indicates the possibility of m
ultiple channel populations formed by homo-oligomeric connexons. These
results suggest that different connexins can be differentially regula
ted by steroid hormones in different cell types, and that the same ste
roid hormone can have different effects on the same connexin in differ
ent cell types.