Difference between revisions of "Anton 2019 Front Physiol"
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|keywords=ISCU, NDUFA4, SDHD, Extravillous trophoblast, miR-210, miRNA, Mitochondrial respiration, Preeclampsia | |keywords=ISCU, NDUFA4, SDHD, Extravillous trophoblast, miR-210, miRNA, Mitochondrial respiration, Preeclampsia | ||
|editor=[[Plangger M]] | |editor=[[Plangger M]] | ||
|mipnetlab=US PA Philadelphia Falk MJ | |||
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|area=Respiration | |area=Respiration, nDNA;cell genetics | ||
|diseases=Other | |||
|organism=Human | |||
|tissues=Genital | |||
|preparations=Permeabilized cells | |||
|couplingstates=LEAK, OXPHOS, ET | |||
|pathways=N, S, NS, ROX | |||
|instruments=Oxygraph-2k | |instruments=Oxygraph-2k | ||
|additional=2020-05 | |additional=2020-05 | ||
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Latest revision as of 16:07, 4 May 2020
Anton L, DeVine A, Polyak E, Olarerin-George A, Brown AG, Falk MJ, Elovitz MA (2019) HIF-1α stabilization increases miR-210 eliciting first trimester extravillous trophoblast mitochondrial dysfunction. Front Physiol 10:699. |
Anton L, DeVine A, Polyak E, Olarerin-George A, Brown AG, Falk MJ, Elovitz MA (2019) Front Physiol
Abstract: Preeclampsia is associated with first trimester placental dysfunction. miR-210, a small non-coding RNA, is increased in the preeclamptic placenta. The effects of elevated miR-210 on placental function remain unclear. The objectives of this study were to identify targets of miR-210 in first trimester primary extravillous trophoblasts (EVTs) and to investigate functional pathways altered by elevated placental miR-210 during early pregnancy. EVTs isolated from first trimester placentas were exposed to cobalt chloride (CoCl2), a HIF-1α stabilizer and hypoxia mimetic, and miR-210 expression by qPCR, HIF1α protein levels by western blot and cell invasion were assessed. A custom TruSeq RNA array, including all known/predicted miR-210 targets, was run using miR-210 and miR-negative control transfected EVTs. Mitochondrial function was assessed by high resolution respirometry in transfected EVTs. EVTs exposed to CoCl2 showed a dose and time-dependent increase in miR-210 and HIF1α and reductions in cell invasion. The TruSeq array identified 49 altered genes in miR-210 transfected EVTs with 27 genes repressed and 22 enhanced. Three of the top six significantly repressed genes, NDUFA4, SDHD, and ISCU, are associated with mitochondrial function. miR-210 transfected EVTs had decreased maximal, complex II and complex I+II mitochondrial respiration. This study suggests that miR-210 alters first trimester trophoblast function. miR-210 overexpression alters EVT mitochondrial function in early pregnancy. Mitochondrial dysfunction may lead to increased reactive oxygen species, trophoblast cell damage and likely contributes to the pathogenesis of preeclampsia. • Keywords: ISCU, NDUFA4, SDHD, Extravillous trophoblast, miR-210, miRNA, Mitochondrial respiration, Preeclampsia • Bioblast editor: Plangger M • O2k-Network Lab: US PA Philadelphia Falk MJ
Labels: MiParea: Respiration, nDNA;cell genetics
Pathology: Other
Organism: Human Tissue;cell: Genital Preparation: Permeabilized cells
Coupling state: LEAK, OXPHOS, ET
Pathway: N, S, NS, ROX
HRR: Oxygraph-2k
2020-05