Journal article
Activating Transcription Factor 3 Is Reduced in Preeclamptic Placentas and Negatively Regulates sFlt-1 (Soluble fms-Like Tyrosine Kinase 1), Soluble Endoglin, and Proinflammatory Cytokines in Placenta
TJ Kaitu'U-Lino, FC Brownfoot, R Hastie, A Chand, P Cannon, M Deo, L Tuohey, C Whitehead, NJ Hannan, S Tong
Hypertension | LIPPINCOTT WILLIAMS & WILKINS | Published : 2017
Abstract
Preeclampsia is a major pregnancy complication associated with poor placental perfusion and placental hypoxia. Systemic and placental inflammation and elevated placental secretion of the antiangiogenic factors sFlt-1 (soluble fms-like tyrosine kinase 1) and sEng (soluble endoglin) are hallmarks of preeclampsia, causing endothelial dysfunction and multiorgan injury. A molecule that links placental hypoxia, inflammation, and antiangiogenic factor release has not been described. ATF3 (activating transcription factor 3) is highly expressed in placenta. We assessed whether placental ATF3 is dysregulated in preterm preeclampsia, is altered by hypoxia, and regulates proinflammatory cytokine and ant..
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Grants
Awarded by National Health and Medical Research Council
Funding Acknowledgements
The National Health and Medical Research Council of Australia provided salary (No. 1062418 to T.J. Kaitu'u-Lino, No. 1050765 to S. Tong, and No. 1062247 to A. Chand). N.J. Hannan salary was provided by CR Roper Fellowship and R. Hastie via APA scholarship. The Olivia Newton-John Cancer Research Institute acknowledges the support of the Victorian Government Infrastructure Support Program.