Basolateral secretions of human endometrial epithelial organoids impact stromal cell decidualization

Author:

Fitzgerald Harriet C12,Kelleher Andrew M3,Ranjit Chaman1,Schust Danny J34,Spencer Thomas E13ORCID

Affiliation:

1. Division of Animal Sciences, University of Missouri , Columbia, MO, USA

2. Present address: The Ritchie Centre, Hudson Institute of Medical Research, Clayton, 3168 Victoria, Australia; Department of Obstetrics and Gynaecology, Monash University, Clayton, 3168 Victoria, Australia

3. Division of Obstetrics, Gynecology and Women’s Health, University of Missouri , Columbia, MO, USA

4. Present address: Department of Obstetrics and Gynecology, Duke University School of Medicine, Durham, NC, USA

Abstract

Abstract Uterine glands and, by inference, their secretions impact uterine receptivity, blastocyst implantation, stromal cell decidualization, and placental development. Changes in gland function across the menstrual cycle are primarily governed by the steroid hormones estrogen (E2) and progesterone (P4) but can also be influenced by extrinsic factors from the stroma. Using a human endometrial epithelial organoid system, transcriptome and proteome analyses identified distinct responses of the organoids to steroid hormones and prostaglandin E2 (PGE2). Notably, P4 and PGE2 modulated the basolateral secretion of organoid proteins, particularly cystatin C (CST3), serpin family A member 3 (SERPINA3), and stanniocalcin 1 (STC1). CST3, but not SERPINA3 or STC1, attenuated the in vitro stromal decidualization response to steroid hormones and PGE2. These findings provide evidence that uterine gland-derived factors impact stromal cell decidualization, which has implications for pregnancy establishment and fertility in women.

Funder

Eunice Kennedy Shriver National Institute of Child Health and Development

NIH

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Obstetrics and Gynecology,Genetics,Molecular Biology,Embryology,Reproductive Medicine

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