Membrane-type MMPs are indispensable for placental labyrinth formation and development

Ludmila Szabova, Mee-Young Son, Joanne Shi, Marek Sramko, Susan S Yamada, William D Swaim, Patricia Zerfas, Stacie Kahan, Kenn Holmbeck

    30 Citations (Scopus)

    Abstract

    The membrane-type matrix metalloproteinases (MT-MMPs) are essential for pericellular matrix remodeling in late stages of development, as well as in growth and tissue homeostasis in postnatal life. Although early morphogenesis is perceived to involve substantial tissue remodeling, the roles of MT-MMPs in these processes are only partially characterized. Here we explore the functions of 2 prominently expressed MT-MMPs, MT1-MMP and MT2-MMP, and describe their roles in the process of placental morphogenesis. The fetal portion of the placenta, in particular the labyrinth (LA), displays strong overlapping expression of MT1-MMP and MT2-MMP, which is critical for syncytiotrophoblast formation and in turn for fetal vessels. Disruption of trophoblast syncytium formation consequently leads to developmental arrest with only a few poorly branched fetal vessels entering the LA causing embryonic death at embryonic day 11.5. Through knockdown of MMP expression, we demonstrate that either MT1-MMP or MT2-MMP is crucial specifically during development of the LA. In contrast, knockdown of MT-MMP activity after LA formation is compatible with development to term and postnatal life. Taken together these data identify essential but interchangeable roles for MT1-MMP or MT2-MMP in placental vasculogenesis and provide the first example of selective temporal and spatial MMP activity required for development of the mouse embryo.

    Original languageEnglish
    JournalBlood
    Volume116
    Issue number25
    Pages (from-to)5752-61
    Number of pages10
    ISSN0006-4971
    DOIs
    Publication statusPublished - 16 Dec 2010

    Keywords

    • Animals
    • Blotting, Western
    • Ear, Inner/embryology
    • Extracellular Matrix/metabolism
    • Female
    • Fluorescent Antibody Technique
    • Immunoenzyme Techniques
    • Matrix Metalloproteinase 14/genetics
    • Matrix Metalloproteinase 15/genetics
    • Mice
    • Placenta/embryology
    • Pregnancy
    • Pregnancy, Animal

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