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PRG2 and AQPEP are misexpressed in fetal membranes in placenta previa and percreta†.
Zhang, Elisa T; Hannibal, Roberta L; Badillo Rivera, Keyla M; Song, Janet H T; McGowan, Kelly; Zhu, Xiaowei; Meinhardt, Gudrun; Knöfler, Martin; Pollheimer, Jürgen; Urban, Alexander E; Folkins, Ann K; Lyell, Deirdre J; Baker, Julie C.
Afiliação
  • Zhang ET; Department of Genetics, Stanford University School of Medicine, Stanford, CA, USA.
  • Hannibal RL; Department of Genetics, Stanford University School of Medicine, Stanford, CA, USA.
  • Badillo Rivera KM; Department of Genetics, Stanford University School of Medicine, Stanford, CA, USA.
  • Song JHT; Department of Genetics, Stanford University School of Medicine, Stanford, CA, USA.
  • McGowan K; Department of Genetics, Stanford University School of Medicine, Stanford, CA, USA.
  • Zhu X; Department of Genetics, Stanford University School of Medicine, Stanford, CA, USA.
  • Meinhardt G; Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA, USA.
  • Knöfler M; Department of Obstetrics and Gynecology, Reproductive Biology Unit, Medical University of Vienna, Vienna, Austria.
  • Pollheimer J; Department of Obstetrics and Gynecology, Reproductive Biology Unit, Medical University of Vienna, Vienna, Austria.
  • Urban AE; Department of Obstetrics and Gynecology, Reproductive Biology Unit, Medical University of Vienna, Vienna, Austria.
  • Folkins AK; Department of Genetics, Stanford University School of Medicine, Stanford, CA, USA.
  • Lyell DJ; Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA, USA.
  • Baker JC; Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
Biol Reprod ; 105(1): 244-257, 2021 07 02.
Article em En | MEDLINE | ID: mdl-33982062
ABSTRACT
The obstetrical conditions placenta accreta spectrum (PAS) and placenta previa are a significant source of pregnancy-associated morbidity and mortality, yet the specific molecular and cellular underpinnings of these conditions are not known. In this study, we identified misregulated gene expression patterns in tissues from placenta previa and percreta (the most extreme form of PAS) compared with control cases. By comparing this gene set with existing placental single-cell and bulk RNA-Seq datasets, we show that the upregulated genes predominantly mark extravillous trophoblasts. We performed immunofluorescence on several candidate molecules and found that PRG2 and AQPEP protein levels are upregulated in both the fetal membranes and the placental disk in both conditions. While this increased AQPEP expression remains restricted to trophoblasts, PRG2 is mislocalized and is found throughout the fetal membranes. Using a larger patient cohort with a diverse set of gestationally aged-matched controls, we validated PRG2 as a marker for both previa and PAS and AQPEP as a marker for only previa in the fetal membranes. Our findings suggest that the extraembryonic tissues surrounding the conceptus, including both the fetal membranes and the placental disk, harbor a signature of previa and PAS that is characteristic of EVTs and that may reflect increased trophoblast invasiveness.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Placenta Acreta / Placenta Prévia / Proteoglicanas / Regulação da Expressão Gênica / Metaloproteases / Proteína Básica Maior de Eosinófilos / Membranas Extraembrionárias Tipo de estudo: Prognostic_studies Limite: Female / Humans / Pregnancy Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Placenta Acreta / Placenta Prévia / Proteoglicanas / Regulação da Expressão Gênica / Metaloproteases / Proteína Básica Maior de Eosinófilos / Membranas Extraembrionárias Tipo de estudo: Prognostic_studies Limite: Female / Humans / Pregnancy Idioma: En Ano de publicação: 2021 Tipo de documento: Article