Death and the desaturase: Implication of Stearoyl-CoA desaturase-1 in the mechanisms of cell stress, apoptosis, and ferroptosis

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-05-31 DOI:10.1016/j.biochi.2024.05.023
R. Ariel Igal
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Abstract

Growth and proliferation of normal and cancerous cells necessitate a finely-tuned regulation of lipid metabolic pathways to ensure the timely supply of structural, energetic, and signaling lipid molecules. The synthesis and remodeling of lipids containing fatty acids with an appropriate carbon length and insaturation level are required for supporting each phase of the mechanisms of cell replication and survival. Mammalian Stearoyl-CoA desaturases (SCD), particularly SCD1, play a crucial role in modulating the fatty acid composition of cellular lipids, converting saturated fatty acids (SFA) into monounsaturated fatty acids (MUFA) in the endoplasmic reticulum (ER). Extensive research has elucidated in great detail the participation of SCD1 in the molecular mechanisms that govern cell replication in normal and cancer cells. More recently, investigations have shed new light on the functional and regulatory role of the Δ9-desaturase in the processes of cell stress and cell death. This review will examine the latest findings on the involvement of SCD1 in the molecular pathways of cell survival, particularly on the mechanisms of ER stress and autophagy, as well in apoptotic and non-apoptotic cell death.

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死亡与不饱和酶:硬脂酰-CoA 不饱和酶-1 在细胞应激、凋亡和铁变态机制中的作用。
正常细胞和癌细胞的生长和增殖需要对脂质代谢途径进行微调,以确保结构、能量和信号脂质分子的及时供应。含有适当碳长和不饱和度的脂肪酸的脂质的合成和重塑是支持细胞复制和存活机制各阶段所必需的。哺乳动物的硬脂酰-CoA 去饱和酶(SCD),尤其是 SCD1,在调节细胞脂质的脂肪酸组成方面起着至关重要的作用,它能在内质网(ER)中将饱和脂肪酸(SFA)转化为单不饱和脂肪酸(MUFA)。大量研究详细阐明了 SCD1 参与正常细胞和癌细胞复制的分子机制。最近的研究又揭示了Δ9-去饱和酶在细胞应激和细胞死亡过程中的功能和调控作用。本综述将探讨 SCD1 参与细胞存活分子途径的最新发现,特别是参与 ER 应激和自噬机制以及细胞凋亡和非凋亡过程的最新发现。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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