Phenotypical modifications of immune cells are enhanced by extracellular matrix

Exp Cell Res. 2021 Aug 15;405(2):112710. doi: 10.1016/j.yexcr.2021.112710. Epub 2021 Jun 24.

Abstract

Immune cells not only constitute tumour microenvironment but they may even affect disease prognosis as a result of dual functional roles that they may play in tumour tissues. Two frequently used established immune cell lines (lymphocytic Jurkat and monocytic THP-1) were used to test whether microenvironmental factors, especially molecular components of extracellular matrix, can shape the phenotype of immune cells. Proliferation, morphological and phenotypical analyses were applied to compare behaviour of the immune cells, typically cultured as suspensions in culture medium, with their behaviour in collagen type I-based and Matrigel-based 3D cultures. Density of both immune cell types in routine suspension cultures affected their subsequent proliferation in extracellular matrices. THP-1 cells appeared to be more sensitive to their surrounding microenvironment as judged from extracellular matrix type-dependent changes in their cell doubling times and from slight increase in their diameters in both extracellular matrix-containing cell cultures. Moreover, even chemically uninduced monocytic THP-1 cells were present in a minor fraction as CD68 positive cell population in collagen type I matrix indicating their partial differentiation to macrophages. Observed modifications of immune cells by microenvironmental factors may have profound implications for their roles in healthy and pathological tissues.

Keywords: 3D cell cultures; Collagen type I; Extracellular matrix; Immune cells; Proliferation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Differentiation / physiology*
  • Cells, Cultured
  • Collagen / metabolism
  • Collagen / pharmacology
  • Collagen Type I / metabolism
  • Drug Combinations
  • Extracellular Matrix / metabolism*
  • Humans
  • Laminin / metabolism
  • Laminin / pharmacology
  • Phenotype*
  • Proteoglycans / metabolism
  • Proteoglycans / pharmacology
  • Tumor Microenvironment / physiology*

Substances

  • Collagen Type I
  • Drug Combinations
  • Laminin
  • Proteoglycans
  • matrigel
  • Collagen