Johnson Renée F, Mitchell Carolyn M, Giles Warwick B, Bisits Andrew, Zakar Tamas
Division of Obstetrics and Gynaecology, John Hunter Hospital, Newcastle, New South Wales, Australia.
J Endocrinol. 2006 Mar;188(3):603-10. doi: 10.1677/joe.1.06488.
Increasing prostaglandin H(2) synthase (PGHS)-2 expression in the fetal membranes is implicated in the production of prostaglandins (PGs) that stimulate labour. We have determined the activity of the PGHS-2 gene in the amnion and chorion throughout gestation and defined the contribution of transcriptional and post-transcriptional mechanisms to the increase of PGHS-2 mRNA levels. We also measured PGHS-1 mRNA abundance to assess the participation of the two isoenzymes in fetal membrane PG-production during pregnancy. Amnion and chorion were collected from non-labouring women at 10-19 weeks (early), at 28-36 weeks (preterm) and at term (37-41 weeks). We determined PGHS-1 and -2 mRNA abundance and assessed PGHS-2 gene activity by measuring PGHS-2 heterogeneous nuclear RNA levels using real-time RT-PCR. PGHS-2 gene activity and mRNA levels were up-regulated in both tissues with advancing gestation. Path analysis demonstrated that the PGHS-2 mRNA up-regulation involved both transcriptional and post-transcriptional components. PGHS-2 mRNA abundance increased 9-11 fold between the early (10-19 weeks) and preterm (28-36 weeks) groups and remained high at term. The underlying mechanism was predominantly transcriptional in the amnion and post-transcriptional in the chorion. PGHS-1 mRNA expression precipitously decreased between early gestation and term. Thus, PGHS-2 mRNA abundance is up-regulated well in advance of term and is not a trigger for labour. There is a switch in PGHS mRNA expression during pregnancy with PGHS-1 dominating in the early period and PGHS-2 dominating at term.
胎膜中前列腺素H(2)合酶(PGHS)-2表达的增加与刺激分娩的前列腺素(PGs)的产生有关。我们已经确定了整个妊娠期羊膜和绒毛膜中PGHS-2基因的活性,并明确了转录和转录后机制对PGHS-2 mRNA水平升高的作用。我们还测量了PGHS-1 mRNA丰度,以评估这两种同工酶在孕期胎膜PG产生中的参与情况。从10-19周(早期)、28-36周(早产)和足月(37-41周)未临产的妇女中收集羊膜和绒毛膜。我们通过实时RT-PCR测量PGHS-2异质核RNA水平来确定PGHS-1和-2 mRNA丰度,并评估PGHS-2基因活性。随着妊娠进展,两种组织中的PGHS-2基因活性和mRNA水平均上调。路径分析表明,PGHS-2 mRNA上调涉及转录和转录后成分。PGHS-2 mRNA丰度在早期(10-19周)和早产(28-36周)组之间增加了9-11倍,并在足月时保持高水平。潜在机制在羊膜中主要是转录性的,在绒毛膜中是转录后性的。PGHS-1 mRNA表达在妊娠早期和足月之间急剧下降。因此,PGHS-2 mRNA丰度在足月前就上调,且不是分娩的触发因素。孕期PGHS mRNA表达存在转换,早期以PGHS-1为主,足月时以PGHS-2为主。