Galectin-3 plays a key role in controlling infection by Toxoplasma gondii in human trophoblast cells and human villous explants

Front Cell Infect Microbiol. 2024 Nov 25:14:1459810. doi: 10.3389/fcimb.2024.1459810. eCollection 2024.

Abstract

Galectin-3 (Gal-3) is a β-galactoside-binding lectin expressed in cells of the placental microenvironment. This lectin is involved in various biological processes, such as modulation of the immune system and control of parasitic illness. Toxoplasma gondii infection can lead to congenital transmission and cause miscarriages, prematurity and fetal anomalies. However, little is known about the role of Gal-3 in T. gondii infection in the placental microenvironment. This study aimed to unravel the underlying mechanisms of Gal-3 during T. gondii infection. For this purpose, we promoted the knockdown of Gal-3 expression by using RNA interference (RNAi) in BeWo cells or by using a synthetic inhibitor (GB1107) in human villous explants. We showed that the decreased Gal-3 expression in BeWo cells and human villous explants increases the invasion and proliferation of T. gondii probably by downregulating MIF and IL6 levels, highlighting thus the role of this lectin in modulating the immune response. Collectively, our study reveals Gal-3 as a promising target protein during congenital toxoplasmosis.

Keywords: Gal-3; congenital toxoplasmosis; immune response; maternal-fetal interface; placental.

MeSH terms

  • Blood Proteins
  • Cell Line
  • Female
  • Galectin 3* / genetics
  • Galectin 3* / metabolism
  • Galectins / genetics
  • Galectins / metabolism
  • Gene Knockdown Techniques
  • Humans
  • Interleukin-6* / metabolism
  • Intramolecular Oxidoreductases
  • Macrophage Migration-Inhibitory Factors* / genetics
  • Macrophage Migration-Inhibitory Factors* / metabolism
  • Placenta / metabolism
  • Placenta / parasitology
  • Pregnancy
  • RNA Interference
  • Toxoplasma*
  • Toxoplasmosis / metabolism
  • Toxoplasmosis / parasitology
  • Trophoblasts* / metabolism
  • Trophoblasts* / parasitology

Substances

  • Galectin 3
  • Macrophage Migration-Inhibitory Factors
  • Interleukin-6
  • MIF protein, human
  • LGALS3 protein, human
  • Galectins
  • IL6 protein, human
  • Blood Proteins
  • Intramolecular Oxidoreductases

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. The authors gratefully acknowledge the Universidade Federal de Uberlândia (UFU), and financial support by Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG), Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq). This study was financed in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior—Brasil (CAPES)—Finance Code 001.