Smad 3 regulates proliferation of the mouse ovarian surface epithelium

被引:14
作者
Symonds, D
Tomic, D
Borgeest, C
McGee, E
Flaws, JA
机构
[1] Univ Maryland, Sch Med, Dept Epidemiol & Prevent Med, Toxicol Program, Baltimore, MD 21201 USA
[2] Univ Pittsburgh, Magee Womens Res Inst, Pittsburgh, PA USA
来源
ANATOMICAL RECORD PART A-DISCOVERIES IN MOLECULAR CELLULAR AND EVOLUTIONARY BIOLOGY | 2003年 / 273A卷 / 02期
关键词
Smad; 3; ovary; surface epithelium; mouse;
D O I
10.1002/ar.a.10090
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Smad 3 is a signaling intermediate for the transforming growth factor beta (TGFbeta) family; however, little is known about the role this protein plays in the regulation of the ovarian surface epithelium (OSE). Using a transgenic mouse model, we found that in the absence of Smad 3 there was a distinct morphological alteration of OSE cells. Wild-type (WT) OSE was flat with thin cells, while Smad 3-deficient (Smad 3 -/-) OSE was thick with plump cuboidal cells. WT OSE had less immunostaining for proliferating cell nuclear antigen (PCNA) and estrogen receptor alpha (ERalpha) than Smad 3 -/- OSE. However, there were no differences in the number of apoptotic cells or Bax and Bcl-2 levels between WT and Smad 3 -/- OSE. Although WT mice had higher levels of serum estradiol than Smad 3 -/- mice, WT and Smad 3 -/- mice had similar levels of progesterone. These data suggest that Smad 3 regulates OSE morphological appearance and proliferation in the absence of high serum estradiol levels or alterations in progesterone levels. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:681 / 686
页数:6
相关论文
共 24 条
  • [1] Mice lacking Smad3 show accelerated wound healing and an impaired local inflammatory response
    Ashcroft, GS
    Yang, X
    Glick, AB
    Weinstein, M
    Letterio, JJ
    Mizel, DE
    Anzano, M
    Greenwell-Wild, T
    Wahl, SM
    Deng, CX
    Roberts, AB
    [J]. NATURE CELL BIOLOGY, 1999, 1 (05) : 260 - 266
  • [2] Ovarian surface epithelium: Biology, endocrinology, and pathology
    Auersperg, N
    Wong, AST
    Choi, KC
    Kang, SK
    Leung, PCK
    [J]. ENDOCRINE REVIEWS, 2001, 22 (02) : 255 - 288
  • [3] Bai WL, 2000, IN VITRO CELL DEV-AN, V36, P657
  • [4] 90-day feeding and one-generation reproduction study in Crl:CD BR rats with 17β-estradiol
    Biegel, LB
    Flaws, JA
    Hirshfield, AN
    O'Connor, JC
    Elliott, GS
    Ladics, GS
    Silbergeld, EK
    Van Pelt, CS
    Hurtt, ME
    Cook, JC
    Frame, SR
    [J]. TOXICOLOGICAL SCIENCES, 1998, 44 (02) : 116 - 142
  • [5] Estradiol up-regulates antiapoptotic Bcl-2 messenger ribonucleic acid and protein in tumorigenic ovarian surface epithelium cells
    Choi, KC
    Kang, SK
    Tai, CJ
    Auersperg, N
    Leung, PCK
    [J]. ENDOCRINOLOGY, 2001, 142 (06) : 2351 - 2360
  • [6] TGFβ-induced Smad signaling remains intact in primary human ovarian cancer cells
    Dunfield, LD
    Dwyer, EJC
    Nachtigal, MW
    [J]. ENDOCRINOLOGY, 2002, 143 (04) : 1174 - 1181
  • [7] HAVRILESKY LJ, 1995, CANCER RES, V55, P944
  • [8] Hayes SA, 2001, CANCER RES, V61, P2112
  • [9] Cloning and studies of the mouse cDNA encoding Smad3
    Kano, K
    Notani, A
    Nam, SY
    Fujisawa, M
    Kurohmaru, M
    Hayashi, Y
    [J]. JOURNAL OF VETERINARY MEDICAL SCIENCE, 1999, 61 (03) : 213 - 219
  • [10] TGFβ signaling in growth control, cancer, and heritable disorders
    Massagué, J
    Blain, SW
    Lo, RS
    [J]. CELL, 2000, 103 (02) : 295 - 309