Characterization of primary models of human trophoblast

Author:

Sheridan Megan A.12ORCID,Zhao Xiaohui23ORCID,Fernando Ridma C.12,Gardner Lucy12,Perez-Garcia Vicente124,Li Qian15,Marsh Steven G. E.67,Hamilton Russell25ORCID,Moffett Ashley12ORCID,Turco Margherita Y.12ORCID

Affiliation:

1. Department of Pathology, University of Cambridge, Cambridge CB2 1QP, UK

2. Centre for Trophoblast Research, University of Cambridge, Cambridge CB2 3EG, UK

3. Department of Physiology, Neuroscience and Development, University of Cambridge, Cambridge CB2 3EG, UK

4. Centro de Investigación Príncipe Felipe, Eduardo Primo Yúfera, Valencia 46012, Spain

5. Department of Genetics, University of Cambridge, Cambridge CB2 3EH, UK

6. Anthony Nolan Research Institute, Royal Free Hospital, London NW3 2QG, UK

7. UCL Cancer Institute, Royal Free Campus, London WC1E 6DD, UK

Abstract

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.

Funder

Royal Society

European Research Council

Centre for Trophoblast Research, University of Cambridge

Ministerio de Ciencia e Innovación

Wellcome Trust

University of Cambridge

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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