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Decidual-type prolactin expression by the human myometrium
B Gellersen1, A Bonhoff, N Hunt
1Institute for Hormone and Fertility Research, Hamburg, Germany.
Endocrinology
|July 1, 1991
Summary
The human myometrium expresses the human prolactin (hPRL) gene, producing a form of hPRL distinct from pituitary hPRL. Progestin significantly inhibits myometrial hPRL expression, suggesting a regulatory role.
Area of Science:
- Reproductive Biology
- Endocrinology
- Molecular Genetics
Background:
- The human myometrium has been proposed as a potential source of uterine prolactin (PRL).
- Immunoreactive PRL has been detected in myometrial explant culture supernatants.
- The precise nature and regulation of PRL production in the myometrium remain to be fully elucidated.
Purpose of the Study:
- To investigate the expression and characteristics of human prolactin (hPRL) in the human myometrium.
- To determine if the myometrium synthesizes PRL and to characterize its transcript and protein.
- To examine the regulation of myometrial hPRL expression by hormones like progestin and estrogen.
Main Methods:
- Northern blot hybridization to detect hPRL mRNA in myometrium.
- Sequence and primer extension analyses to characterize the hPRL transcript.
- Myometrial explant cultures to assess hPRL secretion and regulation.
- Nb2 lymphoma bioassay to determine lactogenic activity.
- Monoclonal antibody neutralization assays.
Main Results:
- The human (h) PRL gene is expressed in the myometrium in vivo, with a transcript larger than pituitary hPRL mRNA.
- Myometrial PRL is identical to pituitary hPRL, but the mRNA originates from alternative transcription initiation.
- Myometrial explants secrete hPRL, including a glycosylated variant (G-hPRL), with significant lactogenic activity.
- hPRL secretion and mRNA abundance are markedly reduced by progestin (medroxy-progesterone acetate) but unaffected by estrogen.
Conclusions:
- The human myometrium is a source of hPRL, utilizing an alternative mRNA transcript.
- Myometrial hPRL production is regulated by progestin, indicating a potential role in uterine function.
- These findings expand our understanding of PRL's extrapituitary sources and regulation within the uterus.