Is there a role for placental senescence in the genesis of obstetric complications and fetal growth restriction? - 28/02/18
Abstract |
The placenta ages as pregnancy advances, yet its continued function is required for a successful pregnancy outcome. Placental aging is a physiological phenomenon; however, there are some placentas that show signs of aging earlier than others. Premature placental senescence and aging are implicated in a number of adverse pregnancy outcomes, including fetal growth restriction, preeclampsia, spontaneous preterm birth, and intrauterine fetal death. Here we discuss cellular senescence, a state of terminal proliferation arrest, and how senescence is regulated. We also explore the role of physiological placental senescence and how aberrant placental senescence alters placental function, contributing to the pathophysiology of fetal growth restriction, preeclampsia, spontaneous preterm labor/birth, and unexplained fetal death.
Le texte complet de cet article est disponible en PDF.Key words : aging, cellular senescence, cyclin-dependent kinase, DNA damage, fetal death, fetal growth restriction, mammalian target of rapamycin complex, membrane rupture, mitogen-activated protein kinase, oxidative stress, phosphoinositide 3-kinase, placental aging, preeclampsia, preterm birth, preterm labor, reactive oxygen species, senescence-associated heterochromatin foci, small for gestational age, stillbirth, telomere, tumor suppressor protein p53, p16, senescence-associated beta-galactosidase, senescence-associated secretory phenotype
The authors report no conflict of interest. |
Vol 218 - N° 2S
P. S762-S773 - février 2018 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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