The Ca2+ concentration impacts the cytokine production of mouse and human lymphoid cells and the polarization of human macrophages in vitro

PLoS One. 2023 Feb 24;18(2):e0282037. doi: 10.1371/journal.pone.0282037. eCollection 2023.

Abstract

Various aspects of the in vitro culture conditions can impact the functional response of immune cells. For example, it was shown that a Ca2+ concentration of at least 1.5 mM during in vitro stimulation is needed for optimal cytokine production by conventional αβ T cells. Here we extend these findings by showing that also unconventional T cells (invariant Natural Killer T cells, mucosal-associated invariant T cells, γδ T cells), as well as B cells, show an increased cytokine response following in vitro stimulation in the presence of elevated Ca2+ concentrations. This effect appeared more pronounced with mouse than with human lymphoid cells and did not influence their survival. A similarly increased cytokine response due to elevated Ca2+ levels was observed with primary human monocytes. In contrast, primary human monocyte-derived macrophages, either unpolarized (M0) or polarized into M1 or M2 macrophages, displayed increased cell death in the presence of elevated Ca2+ concentrations. Furthermore, elevated Ca2+ concentrations promoted phenotypic M1 differentiation by increasing M1 markers on M1 and M2 macrophages and decreasing M2 markers on M2 macrophages. However, the cytokine production of macrophages, again in contrast to the lymphoid cells, was unaltered by the Ca2+ concentration. In summary, our data demonstrate that the Ca2+ concentration during in vitro cultures is an important variable to be considered for functional experiments and that elevated Ca2+ levels can boost cytokine production by both mouse and human lymphoid cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calcium* / metabolism
  • Cell Differentiation
  • Cytokines / metabolism
  • Humans
  • Lymphocytes / metabolism
  • Macrophages* / metabolism
  • Monocytes / metabolism

Substances

  • Calcium
  • Cytokines

Grants and funding

This work was funded by grants from the Scientific and Technological Research Council of Turkey (TUBITAK, #117Z216, GW), the European Molecular Biology Organization (EMBO, #IG3073; GW), and the H2020 Marie Sklodowska-Curie Actions (#777995, GW, DS). The funders had no role in study design, data collection and analysis, decision to publish or preparation of the manuscript.