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Hum. Reprod. Advance Access originally published online on January 24, 2009
Human Reproduction 2009 24(5):1133-1141; doi:10.1093/humrep/den484
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© The Author 2009. 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

Down-regulation of p21-activated kinase 1 by progestin and its increased expression in the eutopic endometrium of women with endometriosis

Sung Hoon Kim1,3, Hoi Woul Lee1, Young Hoon Kim2, Yun Hee Koo1, Hee Dong Chae1, Chung Hoon Kim1, Pil Ryang Lee1 and Byung Moon Kang1

1 Department of Obstetrics and Gynecology, University of Ulsan College of Medicine, Asan Medical Center, 388-1, Pungnap-2dong, Songpa-gu, Seoul 138-736, South Korea 2 Department of Pharmacology, University of Ulsan College of Medicine, Asan Medical Center, Songpa-gu, Seoul 138-736, South Korea

3 Correspondence address. Tel: +82-2-3010-3647; Fax: +82-2-3010-6944; E-mail: kimsung{at}amc.seoul.kr

BACKGROUND: P21-activated kinase 1 (Pak1) integrates various signaling pathways that are vital to cell survival and function. This study was performed to evaluate whether sex steroids may regulate the expression of Pak1 in endometrial cells as well as whether its expression is increased in the eutopic endometrium of women with endometriosis.

METHODS: Following in vitro estradiol (E2) and/or medroxyprogesterone acetate (MPA) treatment of Ishikawa cells and endometrial stromal cells (ESCs), Pak1 protein was analyzed utilizing western blot analysis and immunocytochemistry. Immunohistochemistry was performed to evaluate Pak1 immunoreactivity semiquantitatively in women with endometriosis and in controls. To assess the role of Pak1 on endometrial cell viability, crystal violet assay was performed following transfection of Ishikawa cells with Pak1 small interfering RNA (siRNA).

RESULTS: In vitro treatment with E2 plus MPA or MPA alone led to a significant decrease of Pak1 protein in Ishikawa cells and ESCs (both P < 0.05 versus control). Immunohistochemistry also revealed that Pak1 protein is significantly decreased during the secretory phase in both epithelial and stromal cells in the control subjects (P < 0.001 and P < 0.01, respectively). The immunoreactivity of Pak1 in glandular cells was significantly increased in the eutopic endometrium of women with endometriosis compared with the controls during the secretory phase (P < 0.01). Crystal violet assay has shown that transfection of Ishikawa cells with Pak1 siRNA led to a significant decrease of cellular viability (P < 0.05).

CONCLUSIONS: These findings suggest that Pak1 is down-regulated by progesterone during the secretory phase in normal endometrium and increased Pak1 activity during the secretory phase might lead to establishment of endometriosis.

Key words: P21-activated kinase 1/endometrium/endometriosis/progestin

Submitted on May 30, 2008; resubmitted on December 6, 2008; accepted on December 15, 2008.


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