The EGF repeat and discoidin domain protein, SED1/MFG-E8, is required for mammary gland branching morphogenesis

MA Ensslin, BD Shur - … of the National Academy of Sciences, 2007 - National Acad Sciences
MA Ensslin, BD Shur
Proceedings of the National Academy of Sciences, 2007National Acad Sciences
SED1, also known as MFG-E8, is a secreted protein composed of two EGF repeats (the
second of which contains an RGD motif) and two discoidin/Factor V/VIII C domains. SED1 is
expressed by a wide range of cell types, where it participates in diverse cellular interactions,
such as sperm binding to the egg coat and macrophage recognition of apoptotic
lymphocytes. Although SED1 was originally identified as a milk protein, its function in the
mammary gland remains unclear; suggested functions include inhibition of viral infection …
SED1, also known as MFG-E8, is a secreted protein composed of two EGF repeats (the second of which contains an RGD motif) and two discoidin/Factor V/VIII C domains. SED1 is expressed by a wide range of cell types, where it participates in diverse cellular interactions, such as sperm binding to the egg coat and macrophage recognition of apoptotic lymphocytes. Although SED1 was originally identified as a milk protein, its function in the mammary gland remains unclear; suggested functions include inhibition of viral infection and clearance of apoptotic cells during mammary gland involution. We report here that SED1 has an unexpected obligatory role during mammary gland development. Unlike that seen in WT glands, SED1-null glands show severely reduced branching from epithelial ducts and from terminal end buds, which are thin and poorly developed. SED1 is expressed by both luminal and myoepithelial cells in the developing epithelial duct, and binds to αv integrin receptors on myoepithelial cells leading to MAPK activation and cell proliferation. The absence of SED1 leads to greatly reduced levels of activated MAPK and a concomitant reduction in cell proliferation and branching throughout the epithelial tree. These results suggest that SED1 contributes, at least partly, to the intercellular signaling between luminal and myoepithelial cells that is required for branching morphogenesis.
National Acad Sciences