| Autor: |
Curlewis JD; School of Biomedical Sciences, Department of Physiology and Pharmacology, University of Queensland, Australia. j.curlewis@mailbox.uq.edu.au, Tam SP, Lau P, Kusters DH, Barclay JL, Anderson ST, Waters MJ |
| Jazyk: |
angličtina |
| Zdroj: |
Endocrinology [Endocrinology] 2002 Oct; Vol. 143 (10), pp. 3984-93. |
| DOI: |
10.1210/en.2002-220344 |
| Abstrakt: |
PRL and placental lactogen (PL) play key roles in maintaining the rodent corpus luteum through pregnancy. Suppressors of cytokine signaling (SOCS) have been shown to decrease cell sensitivity to cytokines, including PRL, and so here we have addressed the issue of whether luteolysis induced by prostaglandin F(2alpha) (PGF(2alpha)) might up-regulate SOCS proteins to inhibit PRL signaling. In d 19 pregnant rats, cloprostenol, a PGF(2alpha) analog, rapidly induced transcripts for SOCS-3 and, to a lesser extent, SOCS-1. We also found increased SOCS-3 protein in the ovary by immunoblot and in the corpus luteum by immunohistochemistry. Increased SOCS-3 expression was preceded by an increase in STAT3 tyrosine phosphorylation 10 min after cloprostenol injection and was maintained for 4 h, as determined by gel shift and immunohistochemistry. Induction of SOCS-3 was accompanied by a sharp decrease in active STAT5, as determined by gel-shift assay and by loss of nuclear localized STAT5. Four hours after cloprostenol administration, the corpus luteum was refractory to stimulation of STAT5 by PRL administration, and this was not due to down-regulation of PRL receptor. Therefore, induction of SOCS-3 by PGF(2alpha) may be an important element in the initiation of luteolysis via rapid suppression of luteotropic support from PL. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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