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Tissue-Specific Induction of SOCS Gene Expression by PRL

Department of Physiology and Pharmacology, and Institute for Molecular Bioscience (S.P.T., P.L., M.J.W.), University of Queensland, St. Lucia, Brisbane 4072, Australia; Unite d’Endocrinologie Moleculaire (J.D.), Institute National de la Recherche Agronomique, 78352 Jouy-en-Josas Cedex, France; and The Walter and Eliza Hall Institute of Medical Research and the Cooperative Research Centre for Cellular Growth Factors (D.J.H.), Parkville 3052, Australia

Address all correspondence and requests for reprints to: M. J. Waters, Ph.D., Department of Physiology and Pharmacology, University of Queensland, St. Lucia, Brisbane 4072, Australia. E-mail: m.waters{at}mailbox.uq.edu.au

The mechanisms whereby tissue sensitivity to PRL is controlled are not well understood. Here we report that expression of mRNA and protein for members of the SOCS/CIS/JAB family of cytokine signaling inhibitors is increased by PRL administration in ovary and adrenal gland of the lactating rat deprived of circulating PRL and pups for 24 h but not in mammary gland. Moreover, suckling increases SOCS mRNA in the ovary but not in the mammary gland of pup-deprived rats. Deprivation of PRL and pups for 48 h allows the mammary gland to induce SOCS genes in response to PRL administration, and this is associated with a decrease in basal SOCS-3 mRNA and protein expression to the level seen in other tissues, suggesting that SOCS-3 induced refractoriness related to filling of the gland. In reporter assays, SOCS-1, SOCS-3, and CIS, but not SOCS-2, are able to inhibit transactivation of the STAT 5-responsive ß-lactoglobulin promoter in transient transfection assays. Moreover, suckling results in loss of ovarian and adrenal responsiveness to PRL administered 2 h after commencement of suckling, as determined by STAT 5 gel shift assay. Immunohistochemistry was used to localize the cellular sites of SOCS-3 and CIS protein expression in the ovary and adrenal gland. We propose that induced SOCS-1, SOCS-3, and CIS are actively involved in the cellular inhibitory feedback response to physiological PRL surges in the corpus luteum and adrenal cortex during lactation, but after pup withdrawal, the mammary gland is rendered unresponsive to PRL by increased levels of SOCS-3.

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