The Netrin-4/Laminin γ1/Neogenin-1 complex mediates migration in SK-N-SH neuroblastoma cells

Cell Adh Migr. 2019 Dec;13(1):33-40. doi: 10.1080/19336918.2018.1506652. Epub 2018 Aug 30.

Abstract

Neuroblastoma (NB) is the most common pediatric extracranial solid tumor. It arises during development of the sympathetic nervous system. Netrin-4 (NTN4), a laminin-related protein, has been proposed as a key factor to target NB metastasis, although there is controversy about its function. Here, we show that NTN4 is broadly expressed in tumor, stroma and blood vessels of NB patient samples. Furthermore, NTN4 was shown to act as a cell adhesion molecule required for the migration induced by Neogenin-1 (NEO1) in SK-N-SH neuroblastoma cells. Therefore, we propose that NTN4, by forming a ternary complex with Laminin γ1 (LMγ1) and NEO1, acts as an essential extracellular matrix component, which induces the migration of SK-N-SH cells.

Keywords: Laminin γ1; Neogenin-1; Netrin-4; Neuroblastoma; basal lamina; cell adhesion; cell migration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Adhesion
  • Cell Movement*
  • Female
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Infant
  • Laminin / metabolism*
  • Male
  • Nerve Tissue Proteins / metabolism*
  • Netrins / metabolism*
  • Neuroblastoma / metabolism
  • Neuroblastoma / pathology*
  • Receptors, Cell Surface / metabolism*
  • Tumor Cells, Cultured

Substances

  • Laminin
  • NEO1 protein, human
  • NTN4 protein, human
  • Nerve Tissue Proteins
  • Netrins
  • Receptors, Cell Surface
  • laminin gamma 1

Grants and funding

This work was supported by: FONDECYT 1140697 (VP), 1180495 (VT); CONICYT Fellowships for PhD studies [21130521] (AV).