Stat5 as a target for regulation by extracellular matrix

C. H. Streuli, G. M. Edwards, M. Delcommenne, C. B A Whitelaw, T. G. Burdon, C. Schindler, C. J. Watson

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Transcription of tissue-specific genes in mammary gland requires signals from both prolactin and basement membrane. Here we address the mechanism by which this specialized extracellular matrix regulates transcription. Using mammary cell cultures derived from transgenic mice harboring the ovine β- lactoglobulin gene, we show that either a basement membrane extract, or purified laminin-1, induced high levels of β-lactoglobulin synthesis. It is known that prolactin signals through Stat5 (signal transducer and activator of transcription). This transcription factor interacts with γ-interferon activation site-related motifs within the β-lactoglobulin promoter, which we show are required for matrix dependence of λ-lactoglobulin expression. The DNA binding activity of Stat5 was present only in extracts of mammary cells cultured on basement membrane, indicating that the activation state of Stat5 is regulated by the type of substratum the cell encounters. Thus, basement membrane controls transcription of milk protein genes through the Stat5- mediated prolactin signaling pathway, providing a molecular explanation for previous studies implicating extracellular matrix in the control of mammary differentiation.
    Original languageEnglish
    Pages (from-to)21639-21644
    Number of pages5
    JournalJournal of Biological Chemistry
    Volume270
    Issue number37
    DOIs
    Publication statusPublished - 1995

    Keywords

    • Animals
    • Binding Sites
    • Chloramphenicol O-Acetyltransferase/biosynthesis
    • Collagen/pharmacology
    • Culture Media
    • DNA-Binding Proteins/*metabolism
    • Epithelium/metabolism
    • Extracellular Matrix/*physiology
    • Female
    • Gene Expression Regulation/drug effects
    • Lactoglobulins/*biosynthesis/genetics
    • Laminin/pharmacology
    • Mammary Glands, Animal/*metabolism
    • Mice
    • Mice, Transgenic
    • Pregnancy
    • *Promoter Regions (Genetics)
    • Signal Transduction
    • Support, Non-U.S. Gov't
    • Trans-Activators/*metabolism
    • Transcription Factors/metabolism
    • *Transcription, Genetic
    • Tumor Cells, Cultured

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