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Perfluorobutane sulfonate exposure disrupted human placental cytotrophoblast cell proliferation and invasion involving in dysregulating preeclampsia related genes.
Marinello, William P; Mohseni, Zahra S; Cunningham, Sarah J; Crute, Christine; Huang, Rong; Zhang, Jun J; Feng, Liping.
Afiliação
  • Marinello WP; Department of Obstetrics and Gynecology, Duke University School of Medicine, Durham, NC, USA.
  • Mohseni ZS; Department of Obstetrics and Gynecology, Duke University School of Medicine, Durham, NC, USA.
  • Cunningham SJ; University Program in Genetics and Genomics, Duke University, Durham, NC, USA.
  • Crute C; Department of Obstetrics and Gynecology, Duke University School of Medicine, Durham, NC, USA.
  • Huang R; Integrated Toxicology and Environmental Health Program, Nicholas School of the Environment, Duke University, Durham, NC, USA.
  • Zhang JJ; MOE-Shanghai Key Laboratory of Children's Environmental Health, Xinhua Hospital, Jiao Tong University School of Medicine, Shanghai, China.
  • Feng L; MOE-Shanghai Key Laboratory of Children's Environmental Health, Xinhua Hospital, Jiao Tong University School of Medicine, Shanghai, China.
FASEB J ; 34(11): 14182-14199, 2020 11.
Article em En | MEDLINE | ID: mdl-32901980
ABSTRACT
We reported that maternal PFBS, an emerging pollutant, exposure is positively associated with preeclampsia which can result from aberrant trophoblasts invasion and subsequent placental ischemia. In this study, we investigated the effects of PFBS on trophoblasts proliferation/invasion and signaling pathways. We exposed a human trophoblast line, HTR8/SVneo, to PFBS. Cell viability, proliferation, and cell cycle were evaluated by the MTS assay, Ki-67 staining, and flow cytometry, respectively. We assessed cell migration and invasion with live-cell imaging-based migration assay and matrigel invasion assay, respectively. Signaling pathways were examined by Western blot, RNA-seq, and qPCR. PFBS exposure interrupted cell proliferation and invasion in a dose-dependent manner. PFBS (100 µM) did not cause cell death but instead significant cell proliferation without cell cycle disruption. PFBS (10 and 100 µM) decreased cell migration and invasion, while PFBS (0.1 µM) significantly increased cell invasion but not migration. Further, RNA-seq analysis identified dysregulated HIF-1α target genes that are relevant to cell proliferation/invasion and preeclampsia, while Western Blot data showed the activation of HIF-1α, but not Notch, ERK1/2, (PI3K)AKT, and P38 pathways. PBFS exposure altered trophoblast cell proliferation/invasion which might be mediated by preeclampsia-related genes, suggesting a possible association between prenatal PFBS exposure and adverse placentation.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Placenta / Pré-Eclâmpsia / Ácidos Sulfônicos / Trofoblastos / Regulação da Expressão Gênica / Proliferação de Células / Fluorocarbonos Limite: Female / Humans / Pregnancy Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Placenta / Pré-Eclâmpsia / Ácidos Sulfônicos / Trofoblastos / Regulação da Expressão Gênica / Proliferação de Células / Fluorocarbonos Limite: Female / Humans / Pregnancy Idioma: En Ano de publicação: 2020 Tipo de documento: Article