Hormonal regulation of non-cystic fibrosis transmembrane conductance regulator ion channels in the endocervix

F S Sci. 2023 May;4(2):163-171. doi: 10.1016/j.xfss.2023.03.002. Epub 2023 Mar 11.

Abstract

Objective: To characterize ion channel expression and localization in the endocervix under different hormonal conditions using a nonhuman primate primary endocervical epithelial cell model.

Design: Experimental.

Setting: University-based, translational science laboratory.

Interventions: We cultured and treated conditionally reprogrammed primary rhesus macaque endocervix cells with estradiol and progesterone and measured gene expression changes for several known ion channel and ion channel regulators of mucus secreting epithelia. Using both rhesus macaque endocervical samples and human samples, we localized channels in the endocervix using immunohistochemistry.

Main outcome measures: The relative abundance of transcripts was evaluated using real-time polymerase chain reaction. Immunostaining results were evaluated qualitatively.

Results: Compared with controls, we found that estradiol increased gene expression for ANO6, NKCC1, CLCA1, and PDE4D. Progesterone down-regulated gene expression for ANO6, SCNN1A, SCNN1B, NKCC1, and PDE4D (P≤.05). Immunohistochemistry confirmed endocervical cell membrane localization of ANO1, ANO6, KCNN4, LRR8CA, and NKCC1.

Conclusions: We found several ion channels and ion channel regulators that are hormonally sensitive in the endocervix. These channels, therefore, may play a role in the cyclic fertility changes in the endocervix and could be further investigated as targets for future fertility and contraceptive studies.

Keywords: Ion channels; conditional reprogramming; endocervix; hormones; mucus.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Cervix Uteri* / metabolism
  • Estradiol / pharmacology
  • Female
  • Fibrosis
  • Humans
  • Ion Channels / metabolism
  • Macaca mulatta / metabolism
  • Progesterone*

Substances

  • Progesterone
  • Ion Channels
  • Estradiol