Transcriptome comparisons of trophoblasts from regenerative cell models with peri-implantation human embryos

Author:

Logsdon Deirdre M1,Ming Hao23,Ezashi Toshihiko1,West Rachel C45,Schoolcraft William B1,Roberts R Michael6,Jiang Zongliang23,Yuan Ye1

Affiliation:

1. Colorado Center for Reproductive Medicine , 10290 RidgeGate Circle, Lone Tree, CO 80124, USA

2. Department of Animal Sciences , Genetics Institute, , Gainesville, FL 32610, USA

3. University of Florida , Genetics Institute, , Gainesville, FL 32610, USA

4. Department of Anatomy , Physiology, and Pharmacology, , Auburn, AL 36849, USA

5. Auburn University , Physiology, and Pharmacology, , Auburn, AL 36849, USA

6. Division of Animal Sciences, University of Missouri-Columbia , MO 65211, USA

Abstract

Abstract Mechanisms controlling trophoblast (TB) proliferation and differentiation during embryo implantation are poorly understood. Human trophoblast stem cells (TSC) and BMP4/A83–01/PD173074-treated pluripotent stem cell-derived trophoblast cells (BAP) are two widely employed, contemporary models to study TB development and function, but how faithfully they mimic early TB cells has not been fully examined. We evaluated the transcriptomes of TB cells from BAP and TSC and directly compared them with those from peri-implantation human embryos during extended embryo culture (EEC) between embryonic days 8 to 12. The BAP and TSC grouped closely with TB cells from EEC within each TB sublineage following dimensional analysis and unsupervised hierarchical clustering. However, subtle differences in transcriptional programs existed within each TB sublineage. We also validated the presence of six genes in peri-implantation human embryos by immunolocalization. Our analysis reveals that both BAP and TSC models have features of peri-implantation TB s, while maintaining minor transcriptomic differences, and thus serve as valuable tools for studying implantation in lieu of human embryos.

Funder

Colorado Center for Reproductive Medicine

Publisher

Oxford University Press (OUP)

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