Requirement for proprotein convertase 5/6 during decidualization of human endometrial stromal cells in vitro

被引:52
作者
Okada, H [1 ]
Nie, GY [1 ]
Salamonsen, LA [1 ]
机构
[1] Prince Henrys Inst Med Res, Clayton, Vic 3168, Australia
关键词
D O I
10.1210/jc.2004-0904
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Decidualization of endometrial stromal cells (ESCs) is critical for embryo implantation and maintenance of pregnancy. Proprotein convertase (PC) 5/6 is suggested to play an important role in the processes of stromal cell decidualization and embryo implantation in the mouse. PC5/6 is a member of the PC family responsible for processing precursor proteins to their active forms by selective proteolysis. In this study, we investigated the regulation of PC5/6 mRNA and protein expression in human ESCs during decidualization in vitro. Real-time PCR analyses revealed a significant increase in PC5/6 mRNA levels in ESCs treated with 17beta-estradiol (E-2) plus medroxyprogesterone acetate during decidualization. On the other hand, E2 alone did not increase PC5/6 mRNA expression. Intense PC5/6 immunoreactivity was observed in the cytoplasm of E-2 plus medroxy-progesterone acetate-treated ESCs (decidualized ESCs) compared with E-2-treated ESCs on d 12 of culture (nondecidualized ESCs). This PC5/6 immunoreactivity was abolished by cotreatment with ZK 98299, a progesterone receptor antagonist. Western blotting revealed PC5/6 as approximately 120-kDa bands (pro- and mature forms) and a 65-kDa band (C-terminally truncated form) in decidualized ESCs. Using an antisense morpholino approach, prolactin production, a typical marker for decidualization, was significantly attenuated in decidualized ESCs after treatment with PC5/6 morpholino antisense oligonucleotides in comparison with controls. These results suggest that PC5/6 plays a key role for decidualization in human endometrium.
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收藏
页码:1028 / 1034
页数:7
相关论文
共 33 条
[1]   PC5-A-mediated processing of pro-neurotensin in early compartments of the regulated secretory pathway of PC5-transfected PC12 cells [J].
Barbero, P ;
Rovère, C ;
De Bie, I ;
Seidah, N ;
Beaudet, A ;
Kitabgi, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (39) :25339-25346
[2]   Gene induction and categorical reprogramming during in vitro human endometrial fibroblast decidualization [J].
Brar, AK ;
Handwerger, S ;
Kessler, CA ;
Aronow, BJ .
PHYSIOLOGICAL GENOMICS, 2001, 7 (02) :135-148
[3]   Regulation of bone morphogenetic protein activity by pro domains and proprotein convertases [J].
Constam, DB ;
Robertson, EJ .
JOURNAL OF CELL BIOLOGY, 1999, 144 (01) :139-149
[4]   Interleukin 11 advances progesterone-induced decidualization of human endometrial stromal cells [J].
Dimitriadis, E ;
Robb, L ;
Salamonsen, LA .
MOLECULAR HUMAN REPRODUCTION, 2002, 8 (07) :636-643
[5]   Cyclic AMP and progesterone receptor cross-talk in human endometrium: a decidualizing affair [J].
Gellersen, B ;
Brosens, J .
JOURNAL OF ENDOCRINOLOGY, 2003, 178 (03) :357-372
[6]   IMMUNOHISTOCHEMICAL LOCALIZATION OF EPIDERMAL GROWTH-FACTOR IN HUMAN ENDOMETRIUM, DECIDUA, AND PLACENTA [J].
HOFMANN, GE ;
SCOTT, RT ;
BERGH, PA ;
DELIGDISCH, L .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1991, 73 (04) :882-887
[7]   Uterine and vaginal organ growth requires epidermal growth factor receptor signaling from stroma [J].
Hom, YK ;
Young, P ;
Wiesen, JF ;
Miettinen, PJ ;
Derynck, R ;
Werb, Z ;
Cunha, GR .
ENDOCRINOLOGY, 1998, 139 (03) :913-921
[8]   SEX STEROIDS AND GROWTH-FACTORS DIFFERENTIALLY REGULATE THE GROWTH AND DIFFERENTIATION OF CULTURED HUMAN ENDOMETRIAL STROMAL CELLS [J].
IRWIN, JC ;
UTIAN, WH ;
ECKERT, RL .
ENDOCRINOLOGY, 1991, 129 (05) :2385-2392
[9]   Expression of activin receptors, follistatin and betaglycan by human endometrial stromal cells; consistent with a role for activins during decidualization [J].
Jones, RL ;
Salamonsen, LA ;
Zhao, YC ;
Ethier, JF ;
Drummond, AE ;
Findlay, JK .
MOLECULAR HUMAN REPRODUCTION, 2002, 8 (04) :363-374
[10]   Activin A promotes human endometrial stromal cell decidualization in vitro [J].
Jones, RL ;
Salamonsen, LA ;
Findlay, JK .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (08) :4001-4004