Transcriptional regulation in the placenta during normal and compromised fetal growth

被引:11
作者
Anthony, RV [1 ]
Limesand, SW [1 ]
Jeckel, KM [1 ]
机构
[1] Colorado State Univ, Dept Physiol, Ft Collins, CO 80523 USA
关键词
angiogenesis; hypoxia; intrauterine growth restriction; placental lactogen; transcription;
D O I
10.1042/0300-5127:0290042
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The placenta synthesizes a number of cytokines and growth factors that are involved in the establishment, maintenance or regulation of pregnancy. Included are interferons, placental lactogens, other members of the growth hormone/prolactin gene family, leptin, and an array of angiogenic growth factors. While their roles in pregnancy differ, in their absence pregnancy is either lost or compromised. Therefore an understanding of the cell-specific transcriptional regulation of these genes is imperative if we are ever to alter their expression to benefit pregnancy progression. Our understanding of transcriptional regulation in the placenta is still in its infancy, and there appears to be considerable divergence in the transcriptional regulation of these genes between species, as well as between the various cytokine genes being examined. For example, while there are some commonalities in the regulation of human, rodent and ruminant placental lactogens, there are differences that require the study of placental lactogen gene regulation across species. However, one common theme that is emerging with the angiogenic growth factors, such as vascular endothelial growth factor and the angiopoietins, is the transcriptional control of these genes by oxygen tension within the placenta. Examination of transcriptional regulation in normal and compromised pregnancies will provide additional insight in this area.
引用
收藏
页码:42 / 48
页数:7
相关论文
共 50 条
[1]   COLOCALIZATION OF VASCULAR ENDOTHELIAL GROWTH-FACTOR AND ITS FLT-1 RECEPTOR IN HUMAN PLACENTA [J].
AHMED, A ;
LI, XF ;
DUNK, C ;
WHITTLE, MJ ;
RUSHTON, DI ;
ROLLASON, T .
GROWTH FACTORS, 1995, 12 (03) :235-243
[2]  
AHMED A, 1997, J SOC GYNECOL INVEST, V4, pA663
[3]   The glial cells missing-1 protein is essential for branching morphogenesis in the chorioallantoic placenta [J].
Anson-Cartwright, L ;
Dawson, K ;
Holmyard, D ;
Fisher, SJ ;
Lazzarini, RA ;
Cross, JC .
NATURE GENETICS, 2000, 25 (03) :311-314
[4]  
Anthony RV, 1998, CONT ENDOCRINOL, V9, P461
[5]   Hypoxia-inducible factor-1 mediates the biological effects of oxygen on human trophoblast differentiation through TGFβ3 [J].
Caniggia, I ;
Mostachfi, H ;
Winter, J ;
Gassmann, M ;
Lye, SJ ;
Kuliszewski, M ;
Post, M .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 105 (05) :577-587
[6]   Oxygen and placental development during the first trimester: Implications for the pathophysiology of pre-eclampsia [J].
Caniggia, I ;
Winter, J ;
Lye, SJ ;
Post, M .
PLACENTA, 2000, 21 :S25-S30
[7]   VASCULAR ENDOTHELIAL GROWTH-FACTOR RECEPTOR LOCALIZATION AND ACTIVATION IN HUMAN TROPHOBLAST AND CHORIOCARCINOMA CELLS [J].
CHARNOCKJONES, DS ;
SHARKEY, AM ;
BOOCOCK, CA ;
AHMED, A ;
PLEVIN, R ;
FERRARA, N ;
SMITH, SK .
BIOLOGY OF REPRODUCTION, 1994, 51 (03) :524-530
[8]  
CROSS JC, 1995, DEVELOPMENT, V121, P2513
[9]   Angiopoietin-1 and angiopoietin-2 activate trophoblast Tie-2 to promote growth and migration during placental development [J].
Dunk, C ;
Shams, M ;
Nijjar, S ;
Rhaman, M ;
Qiu, Y ;
Bussolati, B ;
Ahmed, A .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 156 (06) :2185-2199
[10]   DNA-SEQUENCES INVOLVED IN THE TRANSCRIPTIONAL ACTIVATION OF A HUMAN PLACENTAL-LACTOGEN GENE [J].
FITZPATRICK, SL ;
WALKER, WH ;
SAUNDERS, GF .
MOLECULAR ENDOCRINOLOGY, 1990, 4 (12) :1815-1826