Murine trophoblast stem cells (TSCs) are cells isolated from blastocyst stage mouse embryos that are capable of differentiation into multiple trophoblast cell types in vitro and can colonize the placenta in utero. These cells have greatly advanced the study of trophoblast development, due to the ability to expand TSCs and differentiate them in vitro, facilitating cytological, biochemical, and epigenomic studies. However, no well-validated human TSCs have been described, limiting these studies to mouse models. One potential solution that has been pursued by multiple groups is the trans-differentiation of pluripotent stem cells (PSCs), which encompass both embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs), into trophoblast. Although PSCs can trans-differentiate into cells with many features of TSCs, these cells, called trophoblast stem-like cells (TS-LCs), do not have the developmental potential or self-renewal capacity of TSCs. Consequently, TS-LCs are limited as models for trophoblast function. These findings reveal there is an epigenetic block to trans-differentiation that must be overcome to produce bona fide induced trophoblast sem cells (iTSCs) from PSCs. We propose three Aims, two of which will characterize epigenetic features in PSCs that contribute to the trans-differentiation barrier. In the third Aim, we propose to use a combination of genome engineering and a novel hybrid differentiation/trans-differentiation protocol to overcome this barrier and produce bona fide iTSCs. Successful completion of these studies will provide considerable insight into the epigenetic barriers to trans-differentiation, and potentially the first bona fide iTSC lines derived from human PSCs.

Public Health Relevance

Studies of placental disorders are hindered by the absence of a powerful in vitro model of human trophoblast cell differentiation. Trophoblast stem cells (TSCs) isolated from mouse embryos have provided valuable information into the differentiation of trophoblast cell types. However, no well-validated human trophoblast stem cell lines have been described. Trophoblast cells can be trans-differentiated from pluripotent stem cells (PSCs); however, these cells are not fully functional as TSCs. We propose to characterize the epigenetic barriers preventing full trans-differentiation of PSCs to TSCs, and overcome these barriers to produce bona fide induced TSCs (iTSCs) from both human and mouse.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD093783-02
Application #
9607480
Study Section
Molecular Genetics B Study Section (MGB)
Program Officer
Ravindranath, Neelakanta
Project Start
2017-12-02
Project End
2022-11-30
Budget Start
2018-12-01
Budget End
2019-11-30
Support Year
2
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Massachusetts Medical School Worcester
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
603847393
City
Worcester
State
MA
Country
United States
Zip Code
01655
Chu, Feixia; Thornton, Daniel T; Nguyen, Hieu T (2018) Chemical cross-linking in the structural analysis of protein assemblies. Methods 144:53-63