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Elabela and Apelin actions in healthy and pathological pregnancies
Institution:1. Univ. Lille, EA4489 Environnement Périnatal et Santé, F-59000 Lille, France;2. CHU Lille, Jeanne de Flandre Hospital, Gynecology-Obstetrics, F-59000 Lille, France;3. Institut de Recherche en Santé Digestive (IRSD), INSERM U1220, Toulouse, France;4. European Associated Laboratory « NeuroMicrobiota », France;1. Developmental Biology Program, Sloan Kettering Institute, New York, NY 10065, USA;2. Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX 77030, USA;3. The Research Institute of Molecular Pathology, Vienna BioCenter, 1030 Vienna, Austria;4. Life Science Center, Tsukuba Advanced Research Alliance (TARA), University of Tsukuba, Tsukuba 305-8577, Japan;5. Department of Biochemistry and Metabolic Science, Akita University, Akita 010-8543, Japan;6. Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA;7. Terry Fox Laboratory, BC Cancer Agency, Vancouver, BC V5Z 1L3, Canada;3. Jiangsu Key Laboratory for Biodiversity and Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing 210023, China;4. Program of Reproductive and Stem Cell Biology, Department of Ob/Gyn, Stanford University School of Medicine, Stanford, California 94305-5317;1. CHRU of Lille, Jeanne de Flandre Hospital, Gynecology-Obstetrics, Lille, France;2. Univ. Lille, Unité Environnement Périnatal et Santé, EA 4489, Faculté de Médecine, Pôle recherche, IFR 114, 59045 Lille, France;3. University of Lille 1, EA 4489, Villeneuve d''Ascq, France;4. Institut des Maladies Métaboliques et Cardiovasculaires (I2MC), Team 3, INSERM U1048, 31432 Toulouse, France;5. CHRU of Lille, Jeanne de Flandre Hospital, Neonatal Reanimation, Lille, France;1. Ministry of Education-Shanghai Key Laboratory of Children’s Environmental Health, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, 1665 Kongjiang Road, Shanghai 200092, China;2. Department of Obstetrics and Gynecology, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China;3. School of Public Health, Shanghai Jiao Tong University School of Medicine, Shanghai, China;4. Department of Pediatric Cardiology, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, China;5. Department of Obstetrics and Gynecology, Duke University School of Medicine, Durham, NC 27710, USA;1. Office of Women''s Health, Integrative Biosciences Center, Department of Obstetrics and Gynecology and the Department of Physiology, Wayne State University, Detroit, MI 48201, USA;2. Perinatology Research Branch, Department of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, MI, USA;3. Department of Pediatrics, National University of Singapore, Singapore 119260, Singapore
Abstract:Pregnancy is a dynamic and precisely organized process during which one or more baby develops. Embryonic development relies on the formation of the placenta, allowing nutrient and oxygen exchange between the mother and the fetus. Dysfunction of placental formation lead to pregnancy disorders such as preeclampsia (PE) with serious deleterious consequences for fetal and maternal health. Identifying factors involved in fetoplacental homeostasis could inform better diagnostic and therapeutic strategies for these pathological pregnancies. Here, we summarize actions of elabela, apelin and their common receptor APJ in the fetoplacental unit. Studies indicate that elabela is crucial for embryo cardiovascular system formation and early placental development, while apelin acts in mid/late gestation to modulate fetal angiogenesis and energy homeostasis. Most of these findings, drawn from animal models, indicate a key role of elabela/apelin-APJ system in the fetoplacental unit. This review also provides an overview of clinical studies investigating elabela/apelin-APJ system in pathological complicated pregnancies such as PE and gestational diabetes mellitus (GDM). While elabela-deficient mice display all the features of PE, current clinical studies show no difference in circulating elabela levels between PE and control patients which does not support a role in PE development. Conversely, apelin levels are increased during PE, but the use of apelin as an early PE marker remains to be fully investigated.
Keywords:Apelin  Elabela  Placenta  Fetus  Preeclampsia  Gestational diabetes
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