Expression pattern of the CCAAT/enhancer-binding proteins C/EBP-α, C/EBP-β and C/EBP-δ in the human placenta

被引:21
|
作者
Bamberger, AM
Makrigiannakis, A
Schröder, M
Bamberger, CM
Relakis, C
Gellersen, B
Milde-Langosch, K
Löning, T
机构
[1] Univ Hamburg, Hosp Eppendorf, Inst Pathol, Dept Gynecopathol, D-20246 Hamburg, Germany
[2] Univ Hamburg, Hosp Eppendorf, Dept Med, Dept Gynecopathol, D-20246 Hamburg, Germany
[3] Endokrinol Hamburg, Hamburg, Germany
[4] Univ Crete, Sch Med, Dept Obstet & Gynecol, GR-71110 Iraklion, Greece
关键词
CCAAT/enhancer-binding proteins; trophoblast; extravillous trophoblast; placenta; maternal-fetal interface;
D O I
10.1007/s00428-003-0935-7
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The human trophoblast has the capacity to invade maternal tissue in a controlled fashion and to produce a wide range of hormones. The transcription factors belonging to the CCAAT/enhancer-binding protein (C/EBP) family are regulators of intracellular processes and mediators of hormone action. C/EBP binding sites have been described in the promoters of several placenta-expressed target genes. In the present study, we used immunohistochemistry and Western-blot analysis to investigate the expression pattern of the three most important members of this family, C/EBP-alpha, -beta, and -delta, in the normal human placenta as well as in isolated trophoblast cell populations. We found C/EBP-alpha and C/EBP-beta expression in the villous syncytiotrophophoblast (ST) and the extravillous (intermediate) trophoblast (EVT), but it was absent from the villous cytotrophoblast (CT). Interestingly, expression of C/EBP-beta continued to be very strong up to the third trimester of pregnancy, especially in the ST. C/EBP-delta showed overall lower expression levels, stronger only in the EVT, while CT/ST showed very low/negative expression. These data show for the first time the expression pattern and tissue localization of C/EBP factors in the human placenta, indicating that these factors (especially C/EBP-beta) may play important roles in the regulation of placenta-specific genes and processes.
引用
收藏
页码:149 / 152
页数:4
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