Netrin-1 regulates invasion and migration of mouse mammary epithelial cells overexpressing Cripto-1 in vitro and in vivo

J Cell Sci. 2005 Oct 15;118(Pt 20):4633-43. doi: 10.1242/jcs.02574. Epub 2005 Sep 21.

Abstract

The neuronal guidance molecule, Netrin-1, has been suggested to play a role in the adhesion and migration of the mammary gland epithelium. Human and mouse Cripto-1 induce proliferation, migration, invasion and colony formation by epithelial cells in 3D matrices. Here we investigate whether Netrin-1 affects these Cripto-1-dependent activities in mouse mammary epithelial cells. Overexpression of Cripto-1 in EpH4 and HC-11 cells (EpH4/Cripto-1 or HC-11/Cripto-1) was associated with low expression of Netrin-1 and increased expression of its receptor Neogenin compared to that of wild-type cells. No change was observed in the expression of the other Netrin-1 receptor, UNC5H1. Treating EpH4/Cripto-1 or HC-11/Cripto-1 mammary cells with exogenous soluble Netrin-1 resulted in increased expression of E-cadherin and UNC5H1, decreased expression of vimentin and decreased activation of Akt as determined by western blotting. Colony formation by Eph4/Cripto-1 cells in 3D gels was significantly reduced in proximity to a Netrin-1 source, and mammary glands of transgenic mice overexpressing human Cripto-1 showed altered ductal growth in proximity to implanted Netrin-1-releasing pellets. Terminal end buds in the treated transgenic mice mammary glands also showed increased expression of E-cadherin and UNC5H1 and decreased expression of active Akt determined by immunohistochemistry. Together, these results suggest that regulation of Netrin-1 expression is important in regulating Cripto-1-dependent invasion and migration of mammary epithelial cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Cell Movement / physiology*
  • Epidermal Growth Factor / genetics*
  • Epidermal Growth Factor / metabolism*
  • Epithelial Cells / cytology*
  • Epithelial Cells / metabolism*
  • Extracellular Matrix / metabolism
  • Female
  • Gene Expression
  • Humans
  • Mammary Glands, Animal / cytology*
  • Mammary Glands, Animal / growth & development
  • Mammary Glands, Animal / metabolism
  • Mammary Neoplasms, Animal
  • Membrane Glycoproteins / genetics*
  • Membrane Glycoproteins / metabolism*
  • Mesoderm / cytology
  • Mice
  • Mice, Transgenic
  • Morphogenesis
  • Neoplasm Proteins / genetics*
  • Neoplasm Proteins / metabolism*
  • Nerve Growth Factors / metabolism*
  • Netrin Receptors
  • Netrin-1
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • RNA, Small Interfering / genetics
  • RNA, Small Interfering / metabolism
  • Receptors, Cell Surface / metabolism
  • Signal Transduction
  • Tumor Suppressor Proteins / metabolism*

Substances

  • Membrane Glycoproteins
  • NTN1 protein, human
  • Neoplasm Proteins
  • Nerve Growth Factors
  • Netrin Receptors
  • Ntn1 protein, mouse
  • RNA, Messenger
  • RNA, Small Interfering
  • Receptors, Cell Surface
  • Tdgf1 protein, mouse
  • Tumor Suppressor Proteins
  • Unc5A protein, mouse
  • Netrin-1
  • Epidermal Growth Factor