EFFECT OF PROTEIN-SYNTHESIS INHIBITORS AND METABOLIC BLOCKERS ON THE PRODUCTION OF PLACENTAL PROTEINS BY THE INVITRO PERFUSED HUMAN-PLACENTA
EFFECT OF PROTEIN-SYNTHESIS INHIBITORS AND METABOLIC BLOCKERS ON THE PRODUCTION OF PLACENTAL PROTEINS BY THE INVITRO PERFUSED HUMAN-PLACENTA
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DOI:
10.1159/000293763
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发表时间:
1988-01-01
影响因子:
2.1
通讯作者:
SCHNEIDER, H
中科院分区:
文献类型:
--
作者:
BERSINGER, NA;MALEK, A;SCHNEIDER, H
The capacity of the freshly delivered human term placenta to produce and release placental proteins during in vitro dual perfusion was investigated. The organ was perfused in separate closed circulations and aliquots of medium were taken at regular intervals from both maternal and fetal circuits. The placental proteins human chorionic gonadotrophin (HCG), human placental lactogen (HPL), pregnancy-specific .beta.1-glycoprotein (SP1), and pregnancy-associated plasma protein A (PAPP-A) were quantified in these media as well as in the placental tissue before and after the perfusion. It was found that the four above-mentioned proteins were synthesized during the perfusion interval (90 min to 3 h) while pregnancy-associated .alpha.2-glycoprotein and prolactin were only washed out. The mean production of HCG, HPL, SP1, and PAPP-A was decreased when either cycloheximide, puromycin, iodoacetic acid, or 2,4-dinitrophenol had been added to the perfusing medium. Amongst these four antimetabolites iodoacetic acid most severely affected both the total release and net synthesis. It is concluded that the above four proteins are synthesized de novo by the perfused placenta in the absence of maternal tissue and that this synthesis is energy-dependent.