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dc.contributor.authorAhmed, I.en_US
dc.contributor.authorGlynn, B.en_US
dc.contributor.authorPerkins, Anthonyen_US
dc.contributor.authorCastro, MG.en_US
dc.contributor.authorRowe, J.en_US
dc.contributor.authorMorrison, E.en_US
dc.contributor.authorLinton, EA.en_US
dc.date.accessioned2017-05-03T13:44:21Z
dc.date.available2017-05-03T13:44:21Z
dc.date.issued2000en_US
dc.date.modified2007-03-29T07:58:13Z
dc.identifier.issn0021972Xen_US
dc.identifier.doi10.1210/jcem.85.2.6351en_US
dc.identifier.urihttp://hdl.handle.net/10072/3453
dc.description.abstractThis study examined the different molecular forms of CRH in normal and preeclampsia maternal plasma and protease-blocked placental extracts using antibodies to different regions of the CRH precursor, pro-CRH. In the absence of protease inhibitors, chromatographed normal placental extracts contained four peaks of immunoreactivity corresponding to unprocessed approximately 19-kDa pro-CRH, its approximately 8-kDa intermediate metabolite, pro-CRH125-194, its approximately 2.8-kDa midportion fragment, pro-CRH125-151, and 4.75-kDa CRH1-41. However, if protease inhibitors were included in the extraction medium, only pro-CRH and pro-CRH125-194 were found. Pro-CRH processing was more extensive in protease-blocked preeclampsia placentas than in those from normal pregnancy, with three peaks corresponding to pro-CRH, pro-CRH125-194, and mature CRH1-41 peptide found. Using quantitative competitive PCR, the messenger ribonucleic acid levels of CRH precursor in preeclampsia placentas were 1.7-fold higher than those in normal placentas (37.83 ᠳ.48 vs. 21.83 ᠲ.59 attomoles/姠total ribonucleic acid, respectively; P < 0.005). Preeclampsia placentas contained significantly more CRH1-41 cross-reactivity (4.72 ᠱ.22 pmol/g) than normal term placentas (1.52 ᠰ.39 pmol/g; P < 0.048) extracted in medium containing protease inhibitors. The content of pro-CRH125-151-reactive species in these extracts followed the same pattern, with more immunoreactivity detected in preeclampsia placentas (4.23 ᠱ.39 pmol/g) than in those from normal term pregnancies (1.44 ᠰ.32 pmol/g; P < 0.01). Sequential plasma samples from 10 women with normal pregnancy and 5 women with preeclampsia were assayed for pro-CRH125-151- and CRH1-41-immunoreactive species. In normal pregnancy, maternal plasma CRH1-41 immunoreactivity rose with increasing gestational age, reaching 460 ᠴ8 pmol/L at term. In women with preeclampsia, CRH1-41 levels at each gestational age point were higher than those at the equivalent stage of normal pregnancy. In contrast, the levels of pro-CRH125-151-immunoreactive species remained barely detectable throughout normal and preeclamptic pregnancy. Both pro-CRH and CRH1-41, but not pro-CRH125-151, were shown to bind to the plasma CRH-binding protein. Our findings highlight the importance of protection of placental tissue from degrading enzymes during extraction and show that most of the CRH in the human placenta exists as unprocessed pro-CRH, with very little in the form of CRH1-41 except in preeclampsia. Our studies using maternal plasma indicate that CRH1-41 is the only one of the pro-CRH fragments studied to be maintained in significant amounts in the maternal circulation and also the only fragment studied for which a specific plasma binding protein exists.en_US
dc.description.peerreviewedYesen_US
dc.description.publicationstatusYesen_AU
dc.languageEnglishen_US
dc.language.isoen_AU
dc.publisherEndocrine Societyen_US
dc.publisher.placeUSAen_US
dc.relation.ispartofpagefrom755en_US
dc.relation.ispartofpageto764en_US
dc.relation.ispartofjournalJournal of Clinical Endocrinology and Metabolismen_US
dc.relation.ispartofvolume85en_US
dc.subject.fieldofresearchcode320000en_US
dc.titleProcessing of Procorticotrophin-Releasing Hormone (Pro-CRH): Molecular Forms of CRH in Normal and Preeclamptic pregnancyen_US
dc.typeJournal articleen_US
dc.type.descriptionC1 - Peer Reviewed (HERDC)en_US
dc.type.codeC - Journal Articlesen_US
gro.rights.copyrightCopyright 2000 Endocrine Society. Reproduced in accordance with the copyright policy of the publisher. This journal is available online - use hypertext links.en_AU
gro.date.issued2000
gro.hasfulltextNo Full Text


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