EGFR inhibitor AG1478 blocks the formation of 3D structures mainly through ERK signaling pathway in Matrigel-induced 3D reconstruction of eccrine sweat gland-like structures

J Mol Histol. 2020 Apr;51(2):191-197. doi: 10.1007/s10735-020-09869-6. Epub 2020 Mar 26.

Abstract

EGFR signaling plays important roles in the development of eccrine sweat glands. We previously demonstrate that Matrigel induces eccrine sweat gland cells to reconstruct the three-dimensional (3D) structures of eccrine sweat glands, but the mechanisms are still unknown. In the study, eccrine sweat gland cells were cultured within a 3D Matrigel, and EGFR inhibitor AG1478, or MEK1/2 inhibitor U0126, were added to the medium respectively. The morphology of the 3D-reconstructed eccrine sweat gland-like structures was observed, the localization of phospho-EGFR was detected, and protein levels of EGFR, phospho-EGFR, phospho-JAK, phospho-AKT and phospho-ERK were examined. The results showed that cells treatment with AG1478 from Day 0 of 3D cultures blocked formation of spheroid-like structures. AG1478 administration caused reduced phospho-EGFR, concomitant with downregulation of phospho-ERK1/2, but not phospho-JAK or phospho-AKT. Phospho-EGFR and phospho-ERK were reduced, and only a small number of 3D-structures were formed following treatment with U0126. We conclude that EGFR plays important roles in Matrigel-induced 3D structures of eccrine sweat gland-like structures, and ERK1/2 signaling is responsible, at least in part, for the effect of EGFR.

Keywords: ERK signaling pathway; Eccrine sweat glands; Epidermal growth factor receptor; Three-dimensional reconstruction.

MeSH terms

  • Cell Culture Techniques
  • Cells, Cultured
  • Collagen
  • Drug Combinations
  • Eccrine Glands / cytology*
  • ErbB Receptors / antagonists & inhibitors
  • ErbB Receptors / metabolism
  • Humans
  • Janus Kinases / metabolism
  • Laminin
  • MAP Kinase Signaling System / drug effects*
  • Phosphorylation
  • Proteoglycans
  • Proto-Oncogene Proteins c-akt / metabolism
  • Quinazolines / chemistry
  • Quinazolines / pharmacology*
  • Signal Transduction
  • Tyrphostins / chemistry
  • Tyrphostins / pharmacology*

Substances

  • Drug Combinations
  • Laminin
  • Proteoglycans
  • Quinazolines
  • Tyrphostins
  • matrigel
  • RTKI cpd
  • Collagen
  • EGFR protein, human
  • ErbB Receptors
  • Janus Kinases
  • Proto-Oncogene Proteins c-akt