MUC20 expression marks the receptive phase of the human endometrium

Reprod Biomed Online. 2019 Nov;39(5):725-736. doi: 10.1016/j.rbmo.2019.05.004. Epub 2019 May 11.

Abstract

Research question: How does mucin MUC20 expression change during the menstrual cycle in different cell types of human endometrium?

Design: Study involved examination of MUC20 expression in two previously published RNA-seq datasets in whole endometrial tissue (n = 10), sorted endometrial epithelial (n = 44) or stromal (n = 42) cell samples. RNA-Seq results were validated by quantitative reverse transcription polymerase chain reaction (qRT-PCR) in whole tissue (n = 10), sorted epithelial (n = 17) and stromal (n = 17) cell samples. MUC20 protein localization and expression were analysed in human endometrium by immunohistochemical analysis of intact endometrial tissue (n = 6) and also Western blot of cultured stromal and epithelial cells (n = 2).

Results: MUC20 is differentially expressed in the endometrium between the pre-receptive and receptive phases. We show that MUC20 is predominantly expressed by epithelial cells of the receptive endometrium, both at the mRNA (RNA-Seq, P = 0.005; qRT-PCR, P = 0.039) and protein levels (Western blot; immunohistochemistry, P = 0.029).

Conclusion: Our results indicate MUC20 as a novel marker of mid-secretory endometrial biology. We propose a model of MUC20 function in the hepatocyte growth factor (HGF)-activated mesenchymal-epithelial transition (MET) receptor signalling specifically in the receptive phase. Further investigations should reveal the precise function of MUC20 in human endometrium and the possible connection between MUC20 and HGF-activated MET receptor signalling. MUC20 could potentially be included in the list of endometrial receptivity markers after further clinical validation.

Keywords: Endometrium; Implantation; MUC20; Mucin; Receptivity; Window of implantation.

MeSH terms

  • Adult
  • Biopsy
  • Body Mass Index
  • Cytoplasm / metabolism
  • Embryo Implantation
  • Endometrium / metabolism*
  • Epithelial Cells / metabolism
  • Female
  • Gene Expression Regulation*
  • Hepatocyte Growth Factor / metabolism
  • Humans
  • Immunohistochemistry
  • Menstrual Cycle / metabolism*
  • Mucins / metabolism*
  • Proto-Oncogene Proteins c-met / metabolism
  • RNA-Seq

Substances

  • HGF protein, human
  • MUC20 protein, human
  • Mucins
  • Hepatocyte Growth Factor
  • MET protein, human
  • Proto-Oncogene Proteins c-met