The role of cellular senescence in ageing of the placenta

被引:113
|
作者
Cox, Lynne S. [1 ]
Redman, Christopher [2 ]
机构
[1] Univ Oxford, Dept Biochem, South Parks Rd, Oxford OX1 3QU, England
[2] Univ Oxford, John Radcliffe Hosp Oxford, Nuffield Dept Obstet & Gynaecol, Oxford OX3 9DU, England
基金
英国生物技术与生命科学研究理事会; 比尔及梅琳达.盖茨基金会;
关键词
Placenta; Senescence; Syncytiotrophoblast; Decidua; Inflammation; IUGR; Pre-eclampsia; Stillbirth; Senescence-associated secretory phenotype (SASP); Aging; SECRETORY PHENOTYPE; PRETERM DELIVERY; CELLS; MTOR; STILLBIRTH; PREGNANCY; SYNCYTIOTROPHOBLAST; PHOSPHORYLATION; CYTOKINES; SYNCYTIN;
D O I
10.1016/j.placenta.2017.01.116
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Aberrant placental ageing is implicated in a high percentage of birth complications, stillbirths and neonatal deaths. Understanding how this complex organ is established and maintained for the 9-10 months of pregnancy and then how and why it undergoes the physiological changes that result in labour at term is therefore of enormous clinical importance. In this review, we assess the evidence that placental ageing results from cellular senescence, a state of terminal proliferation arrest accompanied by characteristic morphological and metabolic changes including a shift to a pro-inflammatory phenotype. We discuss how senescence both contributes to placental formation during cytotrophoblast fusion, and to the changes necessary for labour onset, such as cervical remodelling and increased sterile inflammatory signalling. Based on evidence from human clinical studies and experimental interventions in mice, we assess possible biochemical pathways that may drive senescence, and speculate on how aberrant senescence in the placenta may contribute to pre-eclampsia, pre-term birth and stillbirth. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:139 / 145
页数:7
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