SENP3 sensitizes macrophages to ferroptosis via de-SUMOylation of FSP1

IF 10.7 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Redox Biology Pub Date : 2024-07-14 DOI:10.1016/j.redox.2024.103267
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Abstract

Ferroptosis, driven by an imbalance in redox homeostasis, has recently been identified to regulate macrophage function and inflammatory responses. SENP3 is a redox-sensitive de-SUMOylation protease that plays an important role in macrophage function. However, doubt remains on whether SENP3 and SUMOylation regulate macrophage ferroptosis. For the first time, the results of our study suggest that SENP3 sensitizes macrophages to RSL3-induced ferroptosis. We showed that SENP3 promotes the ferroptosis of M2 macrophages to decrease M2 macrophage proportion in vivo. Mechanistically, we identified the ferroptosis repressor FSP1 as a substrate for SUMOylation and confirmed that SUMOylation takes place mainly at its K162 site. We found that SENP3 sensitizes macrophages to ferroptosis by interacting with and de-SUMOylating FSP1 at the K162 site. In summary, our study describes a novel type of posttranslational modification for FSP1 and advances our knowledge of the biological functions of SENP3 and SUMOylation in macrophage ferroptosis.

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SENP3 通过 FSP1 的去 SUMOylation 使巨噬细胞对铁变态反应敏感
近来发现,氧化还原平衡失衡所驱动的铁变态反应可调节巨噬细胞的功能和炎症反应。SENP3 是一种对氧化还原反应敏感的去 SUMOylation 蛋白酶,在巨噬细胞功能中发挥着重要作用。然而,SENP3 和 SUMOylation 是否调控巨噬细胞的铁突变仍然存在疑问。我们的研究结果首次表明,SENP3 可使巨噬细胞对 RSL3 诱导的铁突变敏感。我们发现 SENP3 促进了 M2 巨噬细胞的铁凋亡,从而降低了体内 M2 巨噬细胞的比例。从机理上讲,我们发现铁凋亡抑制因子FSP1是SUMO化的底物,并证实SUMO化主要发生在其K162位点。我们发现,SENP3 通过与 FSP1 相互作用并在 K162 位点去 SUMO 化,使巨噬细胞对铁变态反应敏感。总之,我们的研究描述了一种新型的 FSP1 翻译后修饰,增进了我们对 SENP3 和 SUMOylation 在巨噬细胞铁变态反应中的生物学功能的了解。
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来源期刊
Redox Biology
Redox Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
19.90
自引率
3.50%
发文量
318
审稿时长
25 days
期刊介绍: Redox Biology is the official journal of the Society for Redox Biology and Medicine and the Society for Free Radical Research-Europe. It is also affiliated with the International Society for Free Radical Research (SFRRI). This journal serves as a platform for publishing pioneering research, innovative methods, and comprehensive review articles in the field of redox biology, encompassing both health and disease. Redox Biology welcomes various forms of contributions, including research articles (short or full communications), methods, mini-reviews, and commentaries. Through its diverse range of published content, Redox Biology aims to foster advancements and insights in the understanding of redox biology and its implications.
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