SED1/MFG-E8: a bi-motif protein that orchestrates diverse cellular interactions

J Cell Biochem. 2009 Apr 15;106(6):957-66. doi: 10.1002/jcb.22076.

Abstract

MFG-E8 was initially identified as a principle component of the Milk Fat Globule, a membrane-encased collection of proteins and triglycerides that bud from the apical surface of mammary epithelia during lactation. It has since been independently identified in many species and by many investigators and given a variety of names, including p47, lactadherin, rAGS, PAS6/7, and BA-46. The acronym SED1 was proposed to bring cohesion to this nomenclature based upon it being a Secreted protein that contains two distinct functional domains: an N-terminal domain with two EGF-repeats, the second of which has an integrin-binding RGD motif, and a C-terminal domain with two Discoidin/F5/8C domains that bind to anionic phospholipids and/or extracellular matrices. SED1/MFG-E8 is now known to participate in a wide variety of cellular interactions, including phagocytosis of apoptotic lymphocytes and other apoptotic cells, adhesion between sperm and the egg coat, repair of intestinal mucosa, mammary gland branching morphogenesis, angiogenesis, among others. This article will explore the various roles proposed for SED1/MFG-E8, as well as its provocative therapeutic potential.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Alzheimer Disease / metabolism
  • Alzheimer Disease / pathology
  • Amyloid beta-Peptides / metabolism
  • Animals
  • Antigens, Surface / chemistry
  • Antigens, Surface / genetics
  • Antigens, Surface / metabolism*
  • Apoptosis / physiology
  • Atherosclerosis / metabolism
  • Atherosclerosis / pathology
  • Calcium-Binding Proteins
  • Carrier Proteins / metabolism
  • Cell Adhesion Molecules
  • Dendritic Cells / cytology
  • Dendritic Cells / metabolism
  • Epididymis / metabolism
  • Epididymis / ultrastructure
  • Epithelial Cells / cytology
  • Epithelial Cells / physiology
  • Exosomes / metabolism
  • Humans
  • Intestinal Mucosa / metabolism
  • Male
  • Mammary Glands, Human / cytology
  • Mammary Glands, Human / physiology
  • Milk Proteins / chemistry
  • Milk Proteins / genetics
  • Milk Proteins / metabolism*
  • Models, Biological
  • Neovascularization, Physiologic
  • Phagocytosis / physiology
  • Photoreceptor Cells / cytology
  • Photoreceptor Cells / metabolism
  • Protein Conformation
  • Sperm-Ovum Interactions

Substances

  • Amyloid beta-Peptides
  • Antigens, Surface
  • Calcium-Binding Proteins
  • Carrier Proteins
  • Cell Adhesion Molecules
  • EDIL3 protein, human
  • MFGE8 protein, human
  • Milk Proteins