Discovery of novel determinants of endothelial lineage using chimeric heterokaryons

Author:

Wong Wing Tak1,Matrone Gianfranco1ORCID,Tian XiaoYu1,Tomoiaga Simion Alin1,Au Kin Fai12,Meng Shu1,Yamazoe Sayumi3,Sieveking Daniel3,Chen Kaifu1,Burns David M4,Chen James K3,Blau Helen M4,Cooke John P1ORCID

Affiliation:

1. Department of Cardiovascular Sciences, Houston Methodist Research Institute, Houston, United States

2. Department of Internal Medicine, University of Iowa, Iowa City, United States

3. Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, United States

4. Baxter Laboratory for Stem Cell Biology, Stanford University School of Medicine, Stanford, United States

Abstract

We wish to identify determinants of endothelial lineage. Murine embryonic stem cells (mESC) were fused with human endothelial cells in stable, non-dividing, heterokaryons. Using RNA-seq, it is possible to discriminate between human and mouse transcripts in these chimeric heterokaryons. We observed a temporal pattern of gene expression in the ESCs of the heterokaryons that recapitulated ontogeny, with early mesodermal factors being expressed before mature endothelial genes. A set of transcriptional factors not known to be involved in endothelial development was upregulated, one of which was POU class 3 homeobox 2 (Pou3f2). We confirmed its importance in differentiation to endothelial lineage via loss- and gain-of-function (LOF and GOF). Its role in vascular development was validated in zebrafish embryos using morpholino oligonucleotides. These studies provide a systematic and mechanistic approach for identifying key regulators in directed differentiation of pluripotent stem cells to somatic cell lineages.

Funder

American Heart Association

National Institutes of Health

Cancer Prevention and Research Institute of Texas

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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