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本文引用的文献

1
Neurofilaments are the major neuronal target of hydroxynonenal-mediated protein cross-links.神经丝是羟壬烯醛介导的蛋白质交联的主要神经元靶标。
Free Radic Res. 2013 Jul;47(6-7):507-10. doi: 10.3109/10715762.2013.794265. Epub 2013 May 10.
2
Mitochondrial aldehyde dehydrogenase-2 activation prevents β-amyloid-induced endothelial cell dysfunction and restores angiogenesis.线粒体乙醛脱氢酶 2 的激活可预防β-淀粉样蛋白引起的内皮细胞功能障碍并恢复血管生成。
J Cell Sci. 2013 May 1;126(Pt 9):1952-61. doi: 10.1242/jcs.117184. Epub 2013 Feb 27.
3
PDGF-mediated autophagy regulates vascular smooth muscle cell phenotype and resistance to oxidative stress.血小板衍生生长因子介导的自噬调节血管平滑肌细胞表型和对氧化应激的抵抗能力。
Biochem J. 2013 May 1;451(3):375-88. doi: 10.1042/BJ20121344.
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Conformational altered p53 affects neuronal function: relevance for the response to toxic insult and growth-associated protein 43 expression.构象改变的 p53 影响神经元功能:与毒性损伤反应和生长相关蛋白 43 表达相关。
Cell Death Dis. 2013 Feb 7;4(2):e484. doi: 10.1038/cddis.2013.13.
5
Amyloid β-peptide (1-42)-induced oxidative stress in Alzheimer disease: importance in disease pathogenesis and progression.淀粉样β肽(1-42)诱导的阿尔茨海默病氧化应激:在疾病发病机制和进展中的重要性。
Antioxid Redox Signal. 2013 Sep 10;19(8):823-35. doi: 10.1089/ars.2012.5027. Epub 2013 Feb 14.
6
Oxidative stress and lipid peroxidation products in cancer progression and therapy.癌症进展与治疗中的氧化应激和脂质过氧化产物
ISRN Oncol. 2012;2012:137289. doi: 10.5402/2012/137289. Epub 2012 Oct 17.
7
Protein disulfide isomerase modification and inhibition contribute to ER stress and apoptosis induced by oxidized low density lipoproteins.蛋白质二硫键异构酶的修饰与抑制促使氧化型低密度脂蛋白诱导的内质网应激和细胞凋亡。
Antioxid Redox Signal. 2013 Mar 1;18(7):731-42. doi: 10.1089/ars.2012.4577. Epub 2012 Dec 21.
8
The pantheon of the fallen: why are there so many forms of cell death?凋亡之神坛:细胞死亡形式缘何如此多样?
Trends Cell Biol. 2012 Nov;22(11):555-6. doi: 10.1016/j.tcb.2012.08.008. Epub 2012 Sep 17.
9
Inhibition of NF-κB activation by 4-hydroxynonenal contributes to liver injury in a mouse model of alcoholic liver disease.4-羟基壬烯醛通过抑制 NF-κB 激活,有助于酒精性肝病小鼠模型中的肝损伤。
Am J Pathol. 2012 Nov;181(5):1702-10. doi: 10.1016/j.ajpath.2012.08.004. Epub 2012 Sep 13.
10
Naturally occurring variation in the Glutathione-S-Transferase 4 gene determines neurodegeneration after traumatic brain injury.谷胱甘肽-S-转移酶4基因的自然发生变异决定了创伤性脑损伤后的神经退行性变。
Antioxid Redox Signal. 2013 Mar 1;18(7):784-94. doi: 10.1089/ars.2011.4440. Epub 2012 Sep 24.

细胞死亡与氧化应激相关疾病:4-羟基壬烯醛(HNE)的平衡。

Cell death and diseases related to oxidative stress: 4-hydroxynonenal (HNE) in the balance.

机构信息

1] INRA, TOXALIM (Research Centre in Food Toxicology), 180 chemin de Tournefeuille, F-31027 Toulouse, France [2] Université de Toulouse III, INP, ENVT, UPS, TOXALIM, F-31027 Toulouse, France.

出版信息

Cell Death Differ. 2013 Dec;20(12):1615-30. doi: 10.1038/cdd.2013.138. Epub 2013 Oct 4.

DOI:10.1038/cdd.2013.138
PMID:24096871
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3824598/
Abstract

During the last three decades, 4-hydroxy-2-nonenal (HNE), a major α,β-unsaturated aldehyde product of n-6 fatty acid oxidation, has been shown to be involved in a great number of pathologies such as metabolic diseases, neurodegenerative diseases and cancers. These multiple pathologies can be explained by the fact that HNE is a potent modulator of numerous cell processes such as oxidative stress signaling, cell proliferation, transformation or cell death. The main objective of this review is to focus on the different aspects of HNE-induced cell death, with a particular emphasis on apoptosis. HNE is a special apoptotic inducer because of its abilities to form protein adducts and to propagate oxidative stress. It can stimulate intrinsic and extrinsic apoptotic pathways and interact with typical actors such as tumor protein 53, JNK, Fas or mitochondrial regulators. At the same time, due to its oxidant status, it can also induce some cellular defense mechanisms against oxidative stress, thus being involved in its own detoxification. These processes in turn limit the apoptotic potential of HNE. These dualities can imbalance cell fate, either toward cell death or toward survival, depending on the cell type, the metabolic state and the ability to detoxify.

摘要

在过去的三十年中,4-羟基-2-壬烯醛(HNE)作为 n-6 脂肪酸氧化的主要α,β-不饱和醛产物,已被证明与许多病理学有关,如代谢疾病、神经退行性疾病和癌症。这些多种病理学可以通过以下事实来解释:HNE 是许多细胞过程的有效调节剂,如氧化应激信号转导、细胞增殖、转化或细胞死亡。本文的主要目的是集中讨论 HNE 诱导细胞死亡的不同方面,特别强调细胞凋亡。HNE 是一种特殊的凋亡诱导剂,因为它能够形成蛋白质加合物并传播氧化应激。它可以刺激内在和外在的凋亡途径,并与肿瘤蛋白 53、JNK、Fas 或线粒体调节剂等典型因子相互作用。同时,由于其氧化剂状态,它还可以诱导一些细胞对抗氧化应激的防御机制,从而参与自身解毒。这些过程反过来又限制了 HNE 的凋亡潜力。这些双重性可以使细胞命运失衡,无论是朝向细胞死亡还是存活,这取决于细胞类型、代谢状态和解毒能力。