Corticosteroid-binding globulin status at the fetomaternal interface during human term pregnancy

被引:36
作者
Benassayag, C
Souski, I
Mignot, TM
Robert, B
Hassid, J
Duc-Goiran, P
Mondon, F
Rebourcet, R
Dehennin, L
Nunez, EA
Ferré, F
机构
[1] Univ Paris 05, Matern Port Royal Cochin, INSERM, U361, F-75014 Paris, France
[2] Univ Paris 07, Fac Med Xavier Bichat, Lab Biochim Endocrinienne, F-75870 Paris, France
关键词
cortisol; hormone action; parturition; placenta; placental transport; pregnancy; progesterone; steroid hormones;
D O I
10.1095/biolreprod64.3.812
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The status of the corticosteroid-binding globulin (CBG) at the fetomaterial interface, especially in the maternal intervillous blood space (I), was investigated and compared to that of CBC in the maternal (M) and fetal (umbilical arteries [A] and vein M) peripheral circulations at term. Immunoquantitation of plasma CBG showed that the CBG concentration in I was 30% less than that in M (P < 0.001) and threefold higher than that in umbilical cord blood (P < 0.001). The microheterogeneity of CBG studied by immunoaffinoelectrophoresis in the presence of concanavalin A and Western blotting indicated that the CBC in I was mainly of maternal origin and different from fetal CBG. A CBG mRNA, but no classic 50- to 59-kDa CBG, was found in isolated term trophoblastic fens.-The steroid environment of the CBG in I differed greatly from that in the peripheral maternal and fetal circulations, because the progesterone:cortisol molar ratio in I was 75-fold higher than that in M and 7- to 10-fold higher than that in the fetal circulation. Binding studies revealed that the affinity constants of CBG for cortisol in I, A, and V were significantly lower than that in M plasma (P < 0.02) in their respective hormonal contexts. The binding parameters for I-CBC stripped of endogenous steroids and lipids were dose to those for M-CBG but different from those of fetal CBC (P < 0.001). These data reflect the physiological relevance of the CBG-steroid interaction, especially with very CBG-loaded progesterone at the fetomaternal interface during late pregnancy.
引用
收藏
页码:812 / 821
页数:10
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