Keratinocytes negatively regulate the N-cadherin levels of melanoma cells via contact-mediated calcium regulation

Biochem Biophys Res Commun. 2018 Sep 5;503(2):615-620. doi: 10.1016/j.bbrc.2018.06.050. Epub 2018 Jun 14.

Abstract

In human skin, melanocytes and their neighboring keratinocytes have a close functional interrelationship. Keratinocytes, which represent the prevalent cell type of human skin, regulate melanocytes through various mechanisms. Here, we use a keratinocyte and melanoma co-culture system to show for the first time that keratinocytes regulate the cell surface expression of N-cadherin through cell-cell contact. Compared to mono-cultured human melanoma A375 cells, which expressed high levels of N-cadherin, those co-cultured with the HaCaT human keratinocyte cell line showed reduced levels of N-cadherin. This reduction was most evident in areas of A375 cells that underwent cell-cell contact with the HaCaT cells, whereas HaCaT cell-derived extracellular matrix and conditioned medium both failed to reduce N-cadherin levels. The intracellular level of calcium in co-cultured A375 cells was lower than that in mono-cultured A375 cells, and treatment with a cell-permeant calcium chelator (BAPTA) reduced the N-cadherin level of mono-cultured A375 cells. Furthermore, co-culture with HaCaT cells reduced the expression levels of transient receptor potential cation channel (TRPC) 1, -3 and -6 in A375 cells, and siRNA-mediated multi-depletion of TRPC1, -3 and -6 reduced the N-cadherin level in these cells. Taken together, these data suggest that keratinocytes negatively regulate the N-cadherin levels of melanoma cells via cell-to-cell contact-mediated calcium regulation.

Keywords: Cell-cell interaction; Keratinocyte; Melanocyte; Melanoma; N-cadherin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cadherins / metabolism*
  • Calcium / metabolism*
  • Cell Communication*
  • Cell Line
  • Cell Line, Tumor
  • Coculture Techniques
  • Keratinocytes / metabolism
  • Keratinocytes / pathology*
  • Melanoma / metabolism
  • Melanoma / pathology*
  • Mice
  • TRPC Cation Channels / metabolism

Substances

  • Cadherins
  • TRPC Cation Channels
  • Calcium