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4-羟基-7-氧代-5-庚烯酸内酯是人视网膜色素上皮细胞补体途径的有效诱导剂。

4-Hydroxy-7-oxo-5-heptenoic Acid Lactone Is a Potent Inducer of the Complement Pathway in Human Retinal Pigmented Epithelial Cells.

机构信息

Department of Chemistry , Case Western Reserve University , Cleveland , Ohio 44106 , United States.

Department of Biochemistry , Case Western Reserve University , Cleveland , Ohio 44106 , United States.

出版信息

Chem Res Toxicol. 2018 Aug 20;31(8):666-679. doi: 10.1021/acs.chemrestox.8b00028. Epub 2018 Jul 9.

Abstract

We previously discovered that oxidative cleavage of docosahexaenoate (DHA), which is especially abundant in the retinal photoreceptor rod outer segments and retinal pigmented endothelial (RPE) cells, generates 4-hydroxy-7-oxo-5-heptenoate (HOHA) lactone, and that HOHA lactone can enter RPE cells that metabolize it through conjugation with glutathione (GSH). The consequent depletion of GSH results in oxidative stress. We now find that HOHA lactone induces upregulation of the antioxidant transcription factor Nrf2 in ARPE-19 cells. This leads to expression of GCLM, HO1, and NQO1, three known Nrf2-responsive antioxidant genes. Besides this protective response, HOHA lactone also triggers a countervailing inflammatory activation of innate immunity. Evidence for a contribution of the complement pathway to age-related macular degeneration (AMD) pathology includes the presence of complement proteins in drusen and Bruch's membrane from AMD donor eyes, and the identification of genetic susceptibility loci for AMD in the complement pathway. In eye tissues from a mouse model of AMD, accumulation of complement protein in Bruch's membrane below the RPE suggested that the complement pathway targets this interface, where lesions occur in the RPE and photoreceptor rod outer segments. In animal models of AMD, intravenous injection of NaIO to induce oxidative injury selectively destroys the RPE and causes secretion of factor C3 from the RPE into areas directly adjacent to sites of RPE damage. However, a molecular-level link between oxidative injury and complement activation remained elusive. We now find that sub-micromolar concentrations of HOHA lactone foster expression of C3, CFB, and C5 in ARPE-19 cells and induce a countervailing upregulation of CD55, an inhibitor of C3 convertase production and complement cascade amplification. Ultimately, HOHA lactone causes membrane attack complex formation on the plasma membrane. Thus, HOHA lactone provides a molecular-level connection between free-radical-induced oxidative cleavage of DHA and activation of the complement pathway in AMD pathology.

摘要

我们之前发现,二十二碳六烯酸(DHA)的氧化断裂特别丰富存在于视网膜光感受器杆状细胞外段和视网膜色素上皮(RPE)细胞中,生成 4-羟基-7-氧代-5-庚烯酸(HOHA)内酯,HOHA 内酯可以通过与谷胱甘肽(GSH)结合进入代谢它的 RPE 细胞。随之而来的 GSH 耗竭导致氧化应激。我们现在发现,HOHA 内酯在 ARPE-19 细胞中诱导抗氧化转录因子 Nrf2 的上调。这导致 GCLM、HO1 和 NQO1 三种已知的 Nrf2 反应性抗氧化基因的表达。除了这种保护反应外,HOHA 内酯还引发先天免疫的补偿性炎症激活。补体途径对年龄相关性黄斑变性(AMD)病理学的贡献的证据包括 AMD 供体眼中 drusen 和 Bruch 膜中存在补体蛋白,以及补体途径中 AMD 的遗传易感性位点的鉴定。在 AMD 小鼠模型的眼部组织中,RPE 下方 Bruch 膜中补体蛋白的积累表明补体途径靶向该界面,在该界面中 RPE 和光感受器杆状细胞外段发生病变。在 AMD 的动物模型中,静脉注射 NaIO 以诱导氧化损伤选择性地破坏 RPE,并导致因子 C3 从 RPE 分泌到与 RPE 损伤部位直接相邻的区域。然而,氧化损伤和补体激活之间的分子水平联系仍然难以捉摸。我们现在发现,亚微米浓度的 HOHA 内酯促进 ARPE-19 细胞中 C3、CFB 和 C5 的表达,并诱导 CD55 的反向上调,CD55 是 C3 转化酶产生和补体级联放大的抑制剂。最终,HOHA 内酯导致细胞膜攻击复合物在质膜上形成。因此,HOHA 内酯在 AMD 病理学中提供了自由基诱导的 DHA 氧化断裂和补体途径激活之间的分子水平联系。

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1
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Chem Res Toxicol. 2016 Dec 19;29(12):2125-2135. doi: 10.1021/acs.chemrestox.6b00233. Epub 2016 Nov 11.
2
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Chem Res Toxicol. 2016 Jul 18;29(7):1198-210. doi: 10.1021/acs.chemrestox.6b00153. Epub 2016 Jul 7.
3
Parainflammation, chronic inflammation, and age-related macular degeneration.
J Leukoc Biol. 2015 Nov;98(5):713-25. doi: 10.1189/jlb.3RI0615-239R. Epub 2015 Aug 20.
4
Complement System Part I - Molecular Mechanisms of Activation and Regulation.
Front Immunol. 2015 Jun 2;6:262. doi: 10.3389/fimmu.2015.00262. eCollection 2015.
5
Complement regulator CD46: genetic variants and disease associations.
Hum Genomics. 2015 Jun 10;9(1):7. doi: 10.1186/s40246-015-0029-z.
7
Glutathione and thioredoxin antioxidant pathways synergize to drive cancer initiation and progression.
Cancer Cell. 2015 Feb 9;27(2):211-22. doi: 10.1016/j.ccell.2014.11.019. Epub 2015 Jan 22.
8
Complement activation and choriocapillaris loss in early AMD: implications for pathophysiology and therapy.
Prog Retin Eye Res. 2015 Mar;45:1-29. doi: 10.1016/j.preteyeres.2014.11.005. Epub 2014 Dec 5.
9
Cholesterol-mediated activation of acid sphingomyelinase disrupts autophagy in the retinal pigment epithelium.
Mol Biol Cell. 2015 Jan 1;26(1):1-14. doi: 10.1091/mbc.E14-05-1028. Epub 2014 Nov 5.
10
The oxidative stress product carboxyethylpyrrole potentiates TLR2/TLR1 inflammatory signaling in macrophages.
PLoS One. 2014 Sep 3;9(9):e106421. doi: 10.1371/journal.pone.0106421. eCollection 2014.

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