Fertility and Sterility
Volume 91, Issue 5, Supplement , Pages 2199-2209, May 2009

Induction of peritoneal endometriosis in nude mice with use of human immortalized endometriosis epithelial and stromal cells: a potential experimental tool to study molecular pathogenesis of endometriosis in humans

  • Sakhila K. Banu, Ph.D.

      Affiliations

    • Reproductive Endocrinology and Cell Signaling Laboratory, Department of Integrative Biosciences, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, Texas
  • ,
  • Anna Starzinski-Powitz, Ph.D.

      Affiliations

    • Molekulare Zellbiologie und Humangenetik, Institut für Zellbiologie und Neurowissenschaft, Johann Wolfgang Goethe-Universität, Frankfurt am Main, Germany
  • ,
  • V.O. Speights, D.O.

      Affiliations

    • Division of Anatomic Pathology, Department of Pathology, Scott & White Memorial Hospital, Texas A&M University Health Science Center, Temple, Texas
  • ,
  • Robert C. Burghardt, Ph.D.

      Affiliations

    • Department of Integrative Biosciences, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, Texas
  • ,
  • Joe A. Arosh, Ph.D.

      Affiliations

    • Reproductive Endocrinology and Cell Signaling Laboratory, Department of Integrative Biosciences, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, Texas
    • Department of Integrative Biosciences, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, Texas
    • Corresponding Author InformationReprint requests: Joe A. Arosh, Ph.D., Department of Integrative Biosciences, College of Veterinary Medicine & Biomedical Sciences, Mail Stop: TAMU 4458, Texas A&M University, College Station, Texas 77843 (FAX: 979-847-8981).

Received 22 March 2008; received in revised form 25 June 2008; accepted 26 June 2008. published online 22 August 2008.

Objective

To determine whether a mixed population of immortalized human endometriosis epithelial and stromal cells is able to induce peritoneal endometriosis in nude mice.

Design

Prospective experimental study. Human immortalized endometriosis epithelial and stromal cells were xenografted into ovariectomized nude mice. Macroscopically, the number of induced endometriosis-like lesions and their color were determined. Microscopically, histomorphology of endometriosis glands and their structure were analyzed, and comparisons were made with tissue from spontaneous endometriosis in women.

Setting

College of Veterinary Medicine and Biomedical Sciences, Texas A&M University.

Animals

Seven ovariectomized nude mice.

Intervention(s)

Minimal invasive procedures were performed to administer estrogen pellets and transplant immortalized human endometriosis epithelial and stromal cells into nude mice.

Main Outcome Measure(s)

Peritoneal endometriosis-like lesions induced in nude mice were characterized and compared with spontaneous peritoneal endometriosis in women.

Result(s)

Xenografts of human immortalized endometriosis epithelial and stromal cells into the peritoneal cavity of the recipient nude mice are able to proliferate, attach, invade, reorganize, and establish peritoneal endometriosis. Endometriosis glands at different stages of growth were present in induced endometriosis-like lesions. Proliferating cell nuclear antigen, metalloproteinase 2, estrogen receptor-α, cyclooxygenase-2, and prostaglandin E2 receptors EP2 and EP4 proteins were expressed in both endometriosis glandular epithelial and stromal cells of the induced endometriosis-like lesions.

Conclusion(s)

This xenograft model could be used as a potential experimental tool to understand the molecular and cellular aspects of the pathogenesis of endometriosis in humans.

Key Words: Human immortalized endometriosis epithelial and stromal cells, peritoneal endometriosis, xenograft model, nude mice

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 S.K.B. has nothing to disclose. A.S.-P. has nothing to disclose. V.O.S. has nothing to disclose. R.C.B. has nothing to disclose. J.A.A. has nothing to disclose.

 Supported by a program development award to J.A.A. from the Department of Integrative Biosciences, Texas A&M University.

PII: S0015-0282(08)01411-8

doi:10.1016/j.fertnstert.2008.06.050

Fertility and Sterility
Volume 91, Issue 5, Supplement , Pages 2199-2209, May 2009