Characterization of primary models of human trophoblast

Development. 2021 Nov 1;148(21):dev199749. doi: 10.1242/dev.199749. Epub 2021 Nov 5.

Abstract

Two recently developed models, trophoblast organoids and trophoblast stem cells (TSCs), are useful tools to further the understanding of human placental development. Both differentiate from villous cytotrophoblast (VCT) to either extravillous trophoblast (EVT) or syncytiotrophoblast (SCT). Here, we compare the transcriptomes and miRNA profiles of these models to identify which trophoblast they resemble in vivo. Our findings indicate that TSCs do not readily undergo SCT differentiation and closely resemble cells at the base of the cell columns from where EVT derives. In contrast, organoids are similar to VCT and undergo spontaneous SCT differentiation. A defining feature of human trophoblast is that VCT and SCT are human leukocyte antigen (HLA) null, whereas EVT expresses HLA-C, -G and -E molecules. We find that trophoblast organoids retain these in vivo characteristics. In contrast, TSCs express classical HLA-A and HLA-B molecules, and maintain their expression after EVT differentiation, with upregulation of HLA-G. Furthermore, HLA expression in TSCs differs when grown in 3D rather than in 2D, suggesting that mechanical cues are important. Our results can be used to select the most suitable model for the study of trophoblast development, function and pathology.

Keywords: HLA; Models; Primary cells; Trophoblast organoids; Trophoblast stem cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Culture Techniques
  • Cell Differentiation
  • Cells, Cultured
  • Female
  • HLA Antigens / genetics
  • HLA Antigens / metabolism
  • Humans
  • MicroRNAs / genetics
  • MicroRNAs / metabolism
  • Models, Biological*
  • Organoids / cytology
  • Organoids / growth & development
  • Organoids / metabolism
  • Placentation
  • Pregnancy
  • Stem Cells / cytology
  • Stem Cells / metabolism
  • Transcriptome
  • Trophoblasts / cytology*
  • Trophoblasts / metabolism

Substances

  • HLA Antigens
  • MicroRNAs