生物
细胞生物学
磷脂酰乙醇胺
GPX4
程序性细胞死亡
细胞
细胞凋亡
滋养层
磷脂过氧化氢谷胱甘肽过氧化物酶
磷脂
生物化学
氧化应激
膜
磷脂酰胆碱
遗传学
过氧化氢酶
谷胱甘肽过氧化物酶
怀孕
胎儿
胎盘
作者
Kazuhiro Kajiwara,Ofer Beharier,Choon‐Peng Chng,Julie P. Goff,Yingshi Ouyang,Claudette M. St. Croix,Changjin Huang,Valerian E. Kagan,K. Jimmy Hsia,Yoel Sadovsky
摘要
ABSTRACT Ferroptosis is a regulated, non-apoptotic form of cell death, characterized by hydroxy-peroxidation of discrete phospholipid hydroperoxides, particularly hydroperoxyl (Hp) forms of arachidonoyl- and adrenoyl-phosphatidylethanolamine, with a downstream cascade of oxidative damage to membrane lipids, proteins and DNA, culminating in cell death. We recently showed that human trophoblasts are particularly sensitive to ferroptosis caused by depletion or inhibition of glutathione peroxidase 4 (GPX4) or the lipase PLA2G6. Here, we show that trophoblastic ferroptosis is accompanied by a dramatic change in the trophoblast plasma membrane, with macro-blebbing and vesiculation. Immunofluorescence revealed that ferroptotic cell-derived blebs stained positive for F-actin, but negative for cytoplasmic organelle markers. Transfer of conditioned medium that contained detached macrovesicles or co-culture of wild-type target cells with blebbing cells did not stimulate ferroptosis in target cells. Molecular modeling showed that the presence of Hp-phosphatidylethanolamine in the cell membrane promoted its cell ability to be stretched. Together, our data establish that membrane macro-blebbing is characteristic of trophoblast ferroptosis and can serve as a useful marker of this process. Whether or not these blebs are physiologically functional remains to be established. This article has an associated First Person interview with the first author of the paper.
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