Wu Fan, Tian Fu-Ju, Lin Yi
Institute of Embryo-Fetal Original Adult Disease, The International Peace Maternity & Child Health Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200030, China.
Biomed Res Int. 2015;2015:293271. doi: 10.1155/2015/293271. Epub 2015 Nov 29.
During pregnancy, development of the placenta is interrelated with the oxygen concentration. Embryo development takes place in a low oxygen environment until the beginning of the second trimester when large amounts of oxygen are conveyed to meet the growth requirements. High metabolism and oxidative stress are common in the placenta. Reactive oxidative species sometimes harm placental development, but they are also reported to regulate gene transcription and downstream activities such as trophoblast proliferation, invasion, and angiogenesis. Autophagy and apoptosis are two crucial, interconnected processes in the placenta that are often influenced by oxidative stress. The proper interactions between them play an important role in placental homeostasis. However, an imbalance between the protective and destructive mechanisms of autophagy and apoptosis seems to be linked with pregnancy-related disorders such as miscarriage, preeclampsia, and intrauterine growth restriction. Thus, potential therapies to hold oxidative stress in leash, promote placentation, and avoid unwanted apoptosis are discussed.
在怀孕期间,胎盘的发育与氧浓度相互关联。胚胎发育在低氧环境中进行,直到孕中期开始时,大量氧气被输送以满足生长需求。胎盘内高代谢和氧化应激很常见。活性氧有时会损害胎盘发育,但也有报道称它们可调节基因转录及下游活动,如滋养层细胞增殖、侵袭和血管生成。自噬和凋亡是胎盘中两个关键且相互关联的过程,常受氧化应激影响。它们之间的适当相互作用对胎盘稳态起着重要作用。然而,自噬和凋亡的保护与破坏机制之间的失衡似乎与流产、子痫前期和胎儿生长受限等妊娠相关疾病有关。因此,本文讨论了控制氧化应激、促进胎盘形成以及避免不必要凋亡的潜在治疗方法。