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.