Establishment and characterization of immortalized bovine endometrial epithelial cells

Anim Sci J. 2014 Aug;85(8):799-804. doi: 10.1111/asj.12202. Epub 2014 Apr 15.

Abstract

Bovine primary uterine endometrial epithelial cells (EECs) are not ideal for long-term studies, because primary EECs lose hormone responsiveness quickly, and/or they tend to have a short life span. The aims of this study were to establish immortalized bovine EECs and to characterize these cells following long-term cultures. Immortalized bovine EECs were established by transfecting retroviral vectors encoding human papillomavirus (HPV) E6 and E7, and human telomerase reverse transcriptase (hTERT) genes. Established bovine immortalized EECs (imEECs) showed the same morphology as primary EECs, and could be grown without any apparent changes for over 60 passages. In addition, imEECs have maintained the features as EECs, exhibiting oxytocin (OT) and interferon tau (IFNT) responsiveness. Therefore, these imEECs, even after numbers of passages, could be used as an in vitro model to investigate cellular and molecular mechanisms, by which the uterine epithelium responds to IFNT stimulation, the event required for the maternal recognition of pregnancy in the bovine species.

Keywords: bovine; endometrial epithelial cell; immortalization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cattle
  • Cell Proliferation
  • Cell Survival
  • Cells, Cultured
  • Cytological Techniques / methods*
  • Dinoprost
  • Endometrium / cytology*
  • Endometrium / metabolism
  • Female
  • Genetic Vectors
  • Interferon Type I / pharmacology
  • Keratins / metabolism
  • Oncogene Proteins, Viral / genetics
  • Oxytocin / pharmacology
  • Papillomavirus E7 Proteins / genetics
  • Pregnancy
  • Pregnancy Proteins / pharmacology
  • Retroviridae / genetics
  • Stimulation, Chemical
  • Telomerase / genetics
  • Time Factors
  • Transfection
  • Vimentin / metabolism

Substances

  • E6 protein, Human papillomavirus type 6
  • Interferon Type I
  • Oncogene Proteins, Viral
  • Papillomavirus E7 Proteins
  • Pregnancy Proteins
  • Vimentin
  • interferon tau
  • Oxytocin
  • Keratins
  • Dinoprost
  • Telomerase