Prefoldin-5 Expression Is Elevated in Eutopic and Ectopic Endometriotic Epithelium and Modulates Endometriotic Epithelial Cell Proliferation and Migration In Vitro

Author:

Nothnick Warren B.1234,Cui Wei45,Falcone Tommaso6,Graham Amanda1

Affiliation:

1. Department of Cell Biology and Physiology, University of Kansas Medical Center, Kansas City, KS 66160, USA

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

3. Department of Cancer Biology, University of Kansas Medical Center, Kansas City, KS 66160, USA

4. Institute for Reproductive and Developmental Sciences, Center for Reproductive Sciences, University of Kansas Medical Center, Kansas City, KS 66160, USA

5. Department of Pathology and Laboratory Medicine, University of Kansas Medical Center, Kansas City, KS 66160, USA

6. Section of Reproductive Endocrinology and Infertility—Obstetrics and Gynecology Institute, Cleveland Clinic Lerner College of Medicine, Cleveland, OH 44195, USA

Abstract

Endometriosis is a common disease among women of reproductive age in which endometrial tissue grows in ectopic localizations, primarily within the pelvic cavity. These ectopic “lesions” grow as well as migrate and invade underlying tissues. Despite the prevalence of the disease, an understanding of factors that contribute to these cellular attributes remains poorly understood. Prefoldin-5 (PFDN5) has been associated with both aberrant cell proliferation and migration, but a potential role in endometriosis is unknown. As such, the purpose of this study was to examine PFDN5 expression in endometriotic tissue. PFDN5 mRNA and protein were examined in ectopic (lesion) and eutopic endometrial tissue from women with endometriosis and in eutopic endometrium from those without endometriosis using qRT-PCR and immunohistochemistry, respectively, while function of PFDN5 in vitro was evaluated using cell count and migration assays. PFDN5 mRNA and protein were expressed in eutopic and ectopic endometrial tissue, predominantly in the glandular epithelium, but not in endometrium from control subjects. Expression of both mRNA and protein was variable among endometriotic eutopic and ectopic endometrial tissue but showed an overall net increase. Knockdown of PFDN5 by siRNA transfection of endometriotic epithelial 12Z cells was associated with reduced cell proliferation/survival and migration. PFDN5 is expressed in eutopic and ectopic glandular epithelium and may play a role in proliferation and migration of these cells contributing to disease pathophysiology.

Funder

National Institutes of Health/Eunice Kennedy Shriver National Institute of Child Health and Human Development

Publisher

MDPI AG

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