Gene Expression in Human Placenta Following Trauma Exposure Varies Between Boys and Girls

2020 ◽  
Vol 87 (9) ◽  
pp. S292
Author(s):  
Patricia Pehme ◽  
Kaitlin Carson ◽  
Wei Zhang ◽  
Valentina Nikulina ◽  
Yoko Nomura
PLoS ONE ◽  
2010 ◽  
Vol 5 (6) ◽  
pp. e10947 ◽  
Author(s):  
Joana Carvalho Moreira de Mello ◽  
Érica Sara Souza de Araújo ◽  
Raquel Stabellini ◽  
Ana Maria Fraga ◽  
Jorge Estefano Santana de Souza ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Kaitlin E. Bountress ◽  
Vladimir Vladimirov ◽  
Gowon McMichael ◽  
Z. Nathan Taylor ◽  
Gary Hardiman ◽  
...  

Background: The purpose of this study was to identify gene expression differences associated with post-traumatic stress disorder (PTSD) and trauma exposure (TE) in a three-group study design comprised of those with and without trauma exposure and PTSD.Methods: We conducted gene expression and gene network analyses in a sample (n = 45) composed of female subjects of European Ancestry (EA) with PTSD, TE without PTSD, and controls.Results: We identified 283 genes differentially expressed between PTSD-TE groups. In an independent sample of Veterans (n = 78) a small minority of these genes were also differentially expressed. We identified 7 gene network modules significantly associated with PTSD and TE (Bonferroni corrected p ≤ 0.05), which at a false discovery rate (FDR) of q ≤ 0.2, were significantly enriched for biological pathways involved in focal adhesion, neuroactive ligand receptor interaction, and immune related processes among others.Conclusions: This study uses gene network analyses to identify significant gene modules associated with PTSD, TE, and controls. On an individual gene level, we identified a large number of differentially expressed genes between PTSD-TE groups, a minority of which were also differentially expressed in the independent sample. We also demonstrate a lack of network module preservation between PTSD and TE, suggesting that the molecular signature of PTSD and trauma are likely independent of each other. Our results provide a basis for the identification of likely disease pathways and biomarkers involved in the etiology of PTSD.


Placenta ◽  
2010 ◽  
Vol 31 (8) ◽  
pp. 698-704 ◽  
Author(s):  
K.J. Lee ◽  
S.H. Shim ◽  
K.M. Kang ◽  
J.H. Kang ◽  
D.Y. Park ◽  
...  

2018 ◽  
Vol 33 (11) ◽  
pp. 1123-1134 ◽  
Author(s):  
Woong Kim ◽  
Yoon Cho ◽  
Mi-Kyung Song ◽  
Jung-hee Lim ◽  
Jin young Kim ◽  
...  

PLoS ONE ◽  
2016 ◽  
Vol 11 (1) ◽  
pp. e0147013 ◽  
Author(s):  
Ximi K. Wang ◽  
Monica Agarwal ◽  
Nataliya Parobchak ◽  
Alex Rosen ◽  
Anna M. Vetrano ◽  
...  

2003 ◽  
Vol 47 (1) ◽  
pp. 109-116 ◽  
Author(s):  
Xiaohong Zhang ◽  
Takashi Nakaoka ◽  
Toshihide Nishishita ◽  
Nobukazu Watanabe ◽  
Koichi Igura ◽  
...  

2018 ◽  
Vol 103 (4) ◽  
pp. 1545-1557 ◽  
Author(s):  
Sruthi Alahari ◽  
Martin Post ◽  
Alessandro Rolfo ◽  
Rosanna Weksberg ◽  
Isabella Caniggia

Abstract Context The von Hippel Lindau (VHL) protein is a key executor of the cellular hypoxic response that is compromised in preeclampsia, a serious disorder complicating 5% to 7% of pregnancies. To date, the mechanisms controlling VHL gene expression in the human placenta remain elusive. Objective We examined VHL epigenetic regulation in normal pregnancy and in preeclampsia, a pathology characterized by placental hypoxia. Design, Setting, and Participants Placentae were obtained from early-onset preeclampsia (n = 56; <34 weeks of gestation) and late-onset preeclampsia (n = 19; ≥34 weeks of gestation). Placentae from healthy normotensive age-matched preterm control (n = 43) and term control (n = 23) pregnancies were included as controls. Main Outcome Measure(s) We measured the activity of Jumonji domain containing protein 6 (JMJD6), a ferrous iron (Fe2+)– and oxygen-dependent histone demethylase, and examined its function in the epigenetic control of VHL. Results JMJD6 regulates VHL gene expression in the human placenta. VHL downregulation in preeclampsia is dependent on decreased JMJD6 demethylase activity due to hypoxia and reduced Fe2+ bioavailability. Chromatin immunoprecipitation assays revealed decreased association of JMJD6 and its histone targets with the VHL promoter. Findings in preeclampsia were corroborated in a murine model of pharmacological hypoxia using FG-4592. Placentae from FG-4592–treated mice exhibited reduced VHL levels, accompanied by placental morphological alterations and reduced pup weights. Notably, Fe2+ supplementation rescued JMJD6 histone demethylase activity in histone from E-PE and FG-4592–treated mice. Conclusions Our study uncovers epigenetic regulation of VHL and its functional consequences for altered oxygen and iron homeostasis in preeclampsia.


1993 ◽  
Vol 46 (4) ◽  
pp. 497-505 ◽  
Author(s):  
Fernando Larrea ◽  
Lorenza Díaz ◽  
Cecilia Cariño ◽  
Jorge Larriva-Sahdd ◽  
Laura Carrillo ◽  
...  

Placenta ◽  
1996 ◽  
Vol 17 (5-6) ◽  
pp. A3 ◽  
Author(s):  
Carole R. Mendelson ◽  
Kathy H. Graves ◽  
Joseph L. Alcorn ◽  
Cheryl Kunczt ◽  
Margaret E. Smith ◽  
...  

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