The protective effect of apolipoprotein in models of trophoblast invasion and preeclampsia

Author:

Charlton Francesca123,Bobek Gabriele45ORCID,Stait-Gardner Tim45,Price William S.45,Mirabito Colafella Katrina M.6,Xu Bei14,Makris Angela1,Rye Kerry-Anne237,Hennessy Annemarie145

Affiliation:

1. Vascular Immunology Group, The Heart Research Institute, Sydney, New South Wales, Australia;

2. Lipid Research Group, The Heart Research Institute, Sydney, New South Wales, Australia;

3. Sydney Medical School, The University of Sydney, Sydney, New South Wales, Australia;

4. School of Medicine, Western Sydney University, Campbelltown, New South Wales, Australia;

5. Nanoscale Organisation and Dynamics, School of Science and Health, Western Sydney University, Penrith, New South Wales, Australia; and

6. Department of Physiology, Monash University, Melbourne, Victoria, Australia

7. Centre for Vascular Research, University of New South Wales, Sydney, New South Wales, Australia;

Abstract

Preeclampsia is a hypertensive disorder of pregnancy. It is associated with abnormal placentation via poor placental invasion of the uterine vasculature by trophoblast cells, leading to poor placental perfusion, oxidative stress, and inflammation, all of which are implicated in its pathogenesis. A dyslipidemia characterized by low plasma levels of high-density lipoproteins (HDL) and elevated triglycerides has been described in preeclampsia. Apolipoprotein A-I (apoA-I), a constituent of HDL is an anti-inflammatory agent. This study investigated whether apoA-I protects against hypertension and adverse placental changes in a proinflammatory cytokine (TNF-α)-induced model of preeclampsia. Further, this study investigated whether apoA-I protects against the inhibitory effect of TNF-α in a human in vitro model of trophoblast invasion. Administration of apoA-I to pregnant mice before infusion with TNF-α resulted in a significant reduction in the cytokine-induced increase in systolic blood pressure. MRI measurement of T2 relaxation, a parameter that is tissue specific and sensitive to physiological changes within tissues, showed a reversal of TNF-α-induced placental changes. Preincubation of endothelial cells with apoA-I protected against the TNF-α-induced inhibition of HTR-8/SVneo (trophoblast) cell integration into endothelial (UtMVEC) networks. These data suggest that a healthy lipid profile may affect pregnancy outcomes by priming endothelial cells in preparation for trophoblast invasion.

Funder

Department of Health, Australian Government | National Health and Medical Research Council (NHMRC)

Publisher

American Physiological Society

Subject

Physiology (medical),Physiology

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1. Exploration of Serum lipid levels during twin pregnancy;The Journal of Maternal-Fetal & Neonatal Medicine;2023-09-14

2. Death receptor 3 is involved in preeclampsia through regulating placental trophoblast cell physiology by inactivating the PI3K/AKT pathway;Immunity, Inflammation and Disease;2023-09

3. The Influence of Nicotine on Trophoblast-Derived Exosomes in a Mouse Model of Pathogenic Preeclampsia;International Journal of Molecular Sciences;2023-07-05

4. Markers of equine placental differentiation: insights from gene expression studies;Reproduction;2022-03-01

5. Roles of maternal HDL during pregnancy;Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids;2022-03

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