Tissue Eng Regen Med.  2017 Oct;14(5):617-629. 10.1007/s13770-017-0080-z.

Profile of MicroRNA Expression in Endometrial Cell during In Vitro Culture According to Progesterone Concentration

Affiliations
  • 1Department of Obstetrics and Gynecology, Korea University Guro Hospital, 148 Gurodong-ro, Guro-gu, Seoul 08308, Korea.
  • 2Department of Obstetrics and Gynecology, Seoul National University Hospital, 101 Daehak-ro, Jongno-gu, Seoul 03080, Korea. jyhsyk@snu.ac.kr
  • 3Mirae-Heemang Clinic, 68 Jukbong-daero, Seo-gu, Gwangju 61932, Korea.
  • 4Department of Obstetrics and Gynecology, Pusan National University, 179 Gudeok-ro, Seo-gu, Pusan 49241, Korea.
  • 5Department of Obstetrics and Gynecology, Seoul National University College of Medicine, 101 Daehak-ro, Jongno-gu, Seoul 03080, Korea.

Abstract

Artificial uterus using endometrium implant can be a novel treatment strategy for infertile women with refractory endometrial dysfunction. At early pregnancy, the function of uterine endometrial cells for the communication between the conceptus of pre-implantation period and maternal reproductive system is essential. MicroRNA (miR) expression profile of endometrial cells according to progesterone, a crucial pregnancy-maintaining hormone, provides important data for in vitro endometrial cell culture strategy that is useful for engineering artificial uteri using endometrial implants. The present study aimed to evaluate the miR expression profile of in vitro cultured endometrial cells under hormonal milieu mimicking early pregnancy period in terms of progesterone concentration. We cultured murine uterine endometrial cells, human uterine endometrial carcinoma cells, and immortalized human uterine endometrial cells using different progesterone concentrations, and analyzed the expression of miRs critical for early pregnancy. The expression of miR-20a, -21, -196a, -199a, and -200a was differently regulated according to progesterone concentration in different endometrial cell lines. The analysis of candidate target genes showed that the expression of phosphatase and tensin homolog, mucin 1 (MUC1), progesterone receptor, transforming growth factor β receptor II, matrix metallopeptidase-9 was up-regulated by progesterone treatment in mouse and human endometrial cell lines. These results indicate that physiological concentration range (10⁻⁷ and 10⁻⁹ M) of progesterone affect the survival and target gene expression via modulating miR expression. Taken together, progesterone can be a crucial factor in regulating miR expression on in vitro cultured endometrial cells.

Keyword

microRNA; Uterine endometrial cell; Progesterone; Infertile women

MeSH Terms

Animals
Cell Culture Techniques
Cell Line
Endometrial Neoplasms
Endometrium
Female
Gene Expression
Humans
In Vitro Techniques*
Mice
MicroRNAs*
Mucin-1
Pregnancy
Progesterone*
Receptors, Progesterone
Transforming Growth Factors
Uterus
MicroRNAs
Mucin-1
Progesterone
Receptors, Progesterone
Transforming Growth Factors
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