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Hum. Reprod. Advance Access published online on February 5, 2007

Human Reproduction, doi:10.1093/humrep/del514
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© The Author 2007. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Characterization of side-population cells in human normal endometrium

Kiyoko Kato1,5, Momoko Yoshimoto2, Keiji Kato3, Sawako Adachi1, Asako Yamayoshi1, Takahiro Arima1, Kazuo Asanoma1, Satoru Kyo4, Tatsutoshi Nakahata2 and Norio Wake1

1 Department of Molecular Genetics, Division of Molecular and Cell Therapeutics, Medical Institute of Bioregulation, Kyushu University, Higashi-ku, Fukuoka, Japan 2 Department of Pediatrics, Graduate School of Medicine, Kyoto University, Sakyo-ku, Kyoto, Japan 3 Obstetrics & Gynecology, Beppu Medical Center, Beppu, Oita, Japan 4 Department of Obstetrics and Gynecology, School of Medicine, Kanazawa University, Kanazawa, Ishikawa, Japan

5 To whom correspondence should be addressed at: Department of Molecular Genetics, Division of Molecular and Cell Therapeutics, Medical Institute of Bioregulation, Kyushu University, Maidashi 3-1-1, Higashi-ku, Fukuoka, 812-8582, Japan. Tel: 81 92 642 6528; Fax: 81 92 642 6482; E-mail: kkatoh{at}bioreg.kyushu-u.ac.jp

BACKGROUND: It has been proposed that the human endometrium may contain a population of adult stem cells that are responsible for its remarkable regenerative capability. Recently, a subset of stem cells or progenitor cells in adult tissue has been identified as side-population cells (SP cells) displaying low staining with Hoechst 33342 by fluorescence-activated cell sorter (FACS) analysis. In this study, we isolated SP cells from the human endometrium and analysed their properties.

METHOD: Endometrial cells were obtained using enzymatic digestion from uterine hysterectomy for the treatment of uterine myoma and stained with Hoechst 33342 dye either alone or in combination with verapamil. The cells were then analysed using FACS.

RESULTS: SP cells were present among normal human endometrial cells. Most SP cells were enriched in the CD9CD13 fraction. These SP cells showed long-term repopulating properties and produced gland (CD9+)- and stroma (CD13+)-like cells. CD9CD13 cells isolated from the endometrium also generated gland- or stroma-like cells.

CONCLUSIONS: SP cells in the human endometrium can function as progenitor cells. This is the first report of the phenotype of SP cells from normal human endometrial cells.

Key words: CD9/CD13/endometrium/side-population cells/stem cells


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