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Steroids mediate the expression of cytoplasmic and membrane-linked components in human myometrial cells

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UNSPECIFIED (2002) Steroids mediate the expression of cytoplasmic and membrane-linked components in human myometrial cells. MOLECULAR HUMAN REPRODUCTION, 8 (7). pp. 597-605. ISSN 1360-9947

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Abstract

It is well known that the smooth muscle of the human myometrium is a target for the steroid hormones progesterone (P-4) and estrogen. Progesterone is believed to participate in the maintenance of pregnancy, while estrogen is possibly involved in the process of parturition by promoting cervical dilatation. We examined the combined effects of P-4 and 17beta-estradiol (E-2) on components of signalling pathways in human myometrial cells in vitro by immunoblotting. Long-term treatment of myometrial cells with a series of concentrations of P-4 and E-2 in combination caused a change in the phosphorylation status of P42/44 mitogen-activated protein kinase and of c-Jun N-terminal kinase (SAPK/JNK). P-4 and E-2 caused a decrease in protein expression of Gqalpha, Gzalpha, Gi(1/2)alpha and, to a lesser extent, G(0)alpha. The two steroids caused a decrease in the expression of the two small GSalpha isoforms. Cyclo-oxygenase-2 expression was increased by 2.5-fold after steroid treatment, while proliferating cell nuclear antigen expression levels remained unchanged. These observations show that the combination of P-4 and E-2 influences intracellular and membrane-bound components of signal transduction pathways in human myometrial cells. The implications of the two steroid hormones on intracellular signalling pathways in the human myometrium merits further investigation.

Item Type: Journal Article
Subjects: Q Science > QH Natural history > QH301 Biology
R Medicine > RG Gynecology and obstetrics
Journal or Publication Title: MOLECULAR HUMAN REPRODUCTION
Publisher: OXFORD UNIV PRESS
ISSN: 1360-9947
Date: July 2002
Volume: 8
Number: 7
Number of Pages: 9
Page Range: pp. 597-605
Publication Status: Published
URI: http://wrap.warwick.ac.uk/id/eprint/10763

Data sourced from Thomson Reuters' Web of Knowledge

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