Control of integrin expression by extracellular matrix

M. Delcommenne, C. H. Streuli

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Integrin-mediated interactions between cells and the extracellular matrix play a fundamental role in the development and function of a variety of tissues by triggering intracellular signals that regulate gene expression. In this study, mouse mammary epithelial cells plated on tissue culture plastic were shown to dramatically up-regulate the steady state levels of mRNA encoding the α1, α2, α3, α5, α6, α7, α(v), and β1 integrin subunits, in contrast to cells cultured on a basement membrane matrix or cells in vivo. This pattern of expression was also observed in a mouse mammary epithelial strain, CID-9 and in other mouse cell lines such as MMTE cells and K1735-M2 melanoma cells. The control of integrin expression was mediated at different levels in different cell types. In K1735-M2 cells, transcription of the β1 integrin gene was influenced by the substratum, although the levels of integrin protein remained similar. In mammary epithelial cells, the rates of β1 integrin gene transcription were similar, but mRNA and protein levels were higher in cells cultured on plastic than those on basement membrane. For both cell types, the rate of integrin protein turnover was nearly identical in cells cultured on either substratum. Our results demonstrate that extracellular matrix controls the expression of β1 integrin subunits and that this regulation is exerted at both transcriptional and post-transcriptional levels.
    Original languageEnglish
    Pages (from-to)26794-26801
    Number of pages7
    JournalJournal of Biological Chemistry
    Volume270
    Issue number45
    DOIs
    Publication statusPublished - 1995

    Keywords

    • Animals
    • Antigens, CD29/*genetics/metabolism
    • Cell Line
    • Cells, Cultured
    • Epithelium/metabolism
    • Extracellular Matrix/*metabolism
    • Female
    • Gene Expression Regulation
    • Human
    • Mammary Glands, Animal/metabolism
    • Mice
    • RNA, Messenger/genetics/metabolism
    • Support, Non-U.S. Gov't
    • Transcription, Genetic
    • Up-Regulation

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