LPS-Treated Podocytes Polarize Naive CD4+ T Cells into Th17 and Treg Cells

Biomed Res Int. 2020 May 17:2020:8587923. doi: 10.1155/2020/8587923. eCollection 2020.

Abstract

Aim: Our study is aimed at investigating whether Lipopolysaccharide- (LPS-) treated podocytes could polarize naive CD4+ T cells into different subsets in vitro.

Materials and methods: Podocytes and mouse bone marrow-derived dendritic cells (BMDCs) were first cultured with 25 μg/ml LPS for 6 hours, respectively. Then, naive CD4+ T cells were cocultured with the LPS-treated podocytes or BMDCs at a ratio of 1 : 1 or 1 : 1 : 1. After 48 hours, we collected the suspended cells and supernatant from all groups to measure T helper (Th)17 cells, regulatory T (Treg) cells, and cytokine concentration.

Results: We observed the expression of CD80 and major histocompatibility complex class II molecule (MHC II) in podocytes but did not found the upregulation of them after treating podocytes with LPS. LPS-treated podocytes could induce naive CD4+ T cells to Th17 cells and Treg cells with a higher ratio of Th17/Treg than BMDCs. Possible interaction between podocytes and BMDCs may exist in the induction process of Th17 cells and Treg cells.

Conclusion: Our study proved that CD80 and MHC II were constitutively expressed in podocytes but not upregulated by LPS. LPS-treated podocytes could polarize naive CD4+ T cells into Th17 and Treg cells and affect the Th17/Treg balance and may incline to cause a Th17 response.

MeSH terms

  • Animals
  • B7-1 Antigen / metabolism
  • CD4-Positive T-Lymphocytes* / cytology
  • CD4-Positive T-Lymphocytes* / drug effects
  • Cells, Cultured
  • Coculture Techniques
  • Cytokines / metabolism
  • Histocompatibility Antigens Class II / metabolism
  • Lipopolysaccharides / pharmacology*
  • Mice
  • Podocytes* / cytology
  • Podocytes* / drug effects
  • T-Lymphocytes, Regulatory* / cytology
  • T-Lymphocytes, Regulatory* / drug effects
  • Th17 Cells* / cytology
  • Th17 Cells* / drug effects

Substances

  • B7-1 Antigen
  • Cytokines
  • Histocompatibility Antigens Class II
  • Lipopolysaccharides