Netrin-1 can affect morphogenesis and differentiation of the mouse mammary gland

J Cell Physiol. 2008 Sep;216(3):824-34. doi: 10.1002/jcp.21462.

Abstract

Netrin-1 has been shown to regulate the function of the EGF-like protein Cripto-1 (Cr-1) and affect mammary gland development. Since Cr-1 is a target gene of Nanog and Oct4, we investigated the relationship between Netrin-1 and Cr-1, Nanog and Oct4 during different stages of development in the mouse mammary gland. Results from histological analysis show that exogenous Netrin-1 was able to induce formation of alveolar-like structures within the mammary gland terminal end buds of virgin transgenic Cripto-1 mice and enhance mammary gland alveologenesis in early pregnant FVB/N mice. Results from immunostaining and Western blot analysis show that Netrin-1, Nanog and Oct4 are expressed in the mouse embryonic mammary anlage epithelium while Cripto-1 is predominantly expressed outside this structure in the surrounding mesenchyme. We find that in lactating mammary glands of postnatal FVB/N mice, Netrin-1 expression is highest while Cripto-1 and Nanog levels are lowest indicating that Netrin-1 may perform a role in the mammary gland during lactation. HC-11 mouse mammary epithelial cells stimulated with lactogenic hormones and exogenous soluble Netrin-1 showed increased beta-casein expression as compared to control thus supporting the potential role for Netrin-1 during functional differentiation of mouse mammary epithelial cells. Finally, mouse ES cells treated with exogenous soluble Netrin-1 showed reduced levels of Nanog and Cripto-1 and higher levels of beta-III tubulin during differentiation. These results suggest that Netrin-1 may facilitate functional differentiation of mammary epithelial cells and possibly affect the expression of Nanog and/or Cripto-1 in multipotent cells that may reside in the mammary gland.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Animals
  • Caseins / metabolism
  • Cell Differentiation
  • Cells, Cultured
  • Dexamethasone / metabolism
  • Embryonic Stem Cells / cytology
  • Epidermal Growth Factor / genetics
  • Epidermal Growth Factor / metabolism*
  • Female
  • Gene Expression Regulation, Developmental
  • Glucocorticoids / metabolism
  • Homeodomain Proteins / genetics
  • Homeodomain Proteins / metabolism*
  • Insulin / metabolism
  • Lactation
  • Male
  • Mammary Glands, Animal / anatomy & histology
  • Mammary Glands, Animal / growth & development*
  • Mammary Glands, Animal / metabolism
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism*
  • Mice
  • Mice, Transgenic
  • Morphogenesis / physiology*
  • Nanog Homeobox Protein
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / metabolism*
  • Nerve Growth Factors / genetics
  • Nerve Growth Factors / metabolism*
  • Netrin-1
  • Octamer Transcription Factor-3 / genetics
  • Octamer Transcription Factor-3 / metabolism
  • Pregnancy
  • Prolactin / metabolism
  • Tumor Suppressor Proteins / genetics
  • Tumor Suppressor Proteins / metabolism*

Substances

  • Caseins
  • Glucocorticoids
  • Homeodomain Proteins
  • Insulin
  • Membrane Glycoproteins
  • Nanog Homeobox Protein
  • Nanog protein, mouse
  • Neoplasm Proteins
  • Nerve Growth Factors
  • Ntn1 protein, mouse
  • Octamer Transcription Factor-3
  • Pou5f1 protein, mouse
  • Tdgf1 protein, mouse
  • Tumor Suppressor Proteins
  • Netrin-1
  • Epidermal Growth Factor
  • Dexamethasone
  • Prolactin