CITED2 is a conserved regulator of the uterine–placental interface

Author:

Kuna Marija1ORCID,Dhakal Pramod1,Iqbal Khursheed1ORCID,Dominguez Esteban M.1,Kent Lindsey N.1,Muto Masanaga1,Moreno-Irusta Ayelen1,Kozai Keisuke1,Varberg Kaela M.1ORCID,Okae Hiroaki2,Arima Takahiro2ORCID,Sucov Henry M.34ORCID,Soares Michael J.156ORCID

Affiliation:

1. Department of Pathology and Laboratory Medicine, Institute for Reproductive and Developmental Sciences, University of Kansas Medical Center, Kansas City, KS 66160

2. Department of Informative Genetics, Environment and Genome Research Center, Tohoku University Graduate School of Medicine, Sendai 980-8575, Japan

3. Department of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, SC 29425

4. Division of Cardiology, Department of Medicine, Medical University of South Carolina, Charleston, SC 29425

5. Department of Obstetrics and Gynecology, University of Kansas Medical Center, Kansas City, KS 66160

6. Center for Perinatal Research, Children’s Research Institute, Children’s Mercy, Kansas City, MO 64108

Abstract

Establishment of the hemochorial uterine–placental interface requires exodus of trophoblast cells from the placenta and their transformative actions on the uterus, which represent processes critical for a successful pregnancy, but are poorly understood. We examined the involvement of CBP/p300-interacting transactivator with glutamic acid/aspartic acid-rich carboxyl-terminal domain 2 (CITED2) in rat and human trophoblast cell development. The rat and human exhibit deep hemochorial placentation. CITED2 was distinctively expressed in the junctional zone (JZ) and invasive trophoblast cells of the rat. Homozygous Cited2 gene deletion resulted in placental and fetal growth restriction. Small Cited2 null placentas were characterized by disruptions in the JZ, delays in intrauterine trophoblast cell invasion, and compromised plasticity. In the human placentation site, CITED2 was uniquely expressed in the extravillous trophoblast (EVT) cell column and importantly contributed to the development of the EVT cell lineage. We conclude that CITED2 is a conserved regulator of deep hemochorial placentation.

Funder

Kansas IDeA Network of Biomedical Research Excellence

Lalor Foundation

American Heart Association

HHS | National Institutes of Health

HHS | NIH | Eunice Kennedy Shriver National Institute of Child Health and Human Development

The Sosland Foundation

KUMC Biomedical Training Program

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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