• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Targeting a Braf/Mapk pathway rescues podocyte lipid peroxidation in CoQ-deficiency kidney disease.靶向 Braf/Mapk 通路可挽救 CoQ 缺乏症肾病中足细胞的脂质过氧化。
J Clin Invest. 2021 Mar 1;131(5). doi: 10.1172/JCI141380.
2
CoQ supplementation rescues nephrotic syndrome through normalization of HS oxidation pathway.辅酶 Q 补充通过使 HS 氧化途径正常化来挽救肾病综合征。
Biochim Biophys Acta Mol Basis Dis. 2018 Nov;1864(11):3708-3722. doi: 10.1016/j.bbadis.2018.09.002. Epub 2018 Sep 6.
3
Coenzyme Q biosynthesis in health and disease.健康与疾病中的辅酶Q生物合成
Biochim Biophys Acta. 2016 Aug;1857(8):1079-1085. doi: 10.1016/j.bbabio.2016.03.036. Epub 2016 Apr 7.
4
Primary coenzyme Q deficiency in Pdss2 mutant mice causes isolated renal disease.Pdss2突变小鼠中的原发性辅酶Q缺乏导致孤立性肾病。
PLoS Genet. 2008 Apr 25;4(4):e1000061. doi: 10.1371/journal.pgen.1000061.
5
Metabolism of the Flavonol Kaempferol in Kidney Cells Liberates the B-ring to Enter Coenzyme Q Biosynthesis.黄酮醇山柰酚在肾细胞中的代谢将 B 环释放出来进入辅酶 Q 生物合成。
Molecules. 2020 Jun 27;25(13):2955. doi: 10.3390/molecules25132955.
6
Coenzyme Q deficiencies: pathways in yeast and humans.辅酶 Q 缺乏症:酵母和人类中的途径。
Essays Biochem. 2018 Jul 20;62(3):361-376. doi: 10.1042/EBC20170106.
7
GDC-0879, a BRAF Inhibitor, Protects Kidney Podocytes from Death.GDC-0879,一种 BRAF 抑制剂,可保护肾脏足细胞免于死亡。
Cell Chem Biol. 2018 Feb 15;25(2):175-184.e4. doi: 10.1016/j.chembiol.2017.11.006. Epub 2017 Dec 14.
8
Human COQ10A and COQ10B are distinct lipid-binding START domain proteins required for coenzyme Q function.人类 COQ10A 和 COQ10B 是不同的脂质结合 START 结构域蛋白,对于辅酶 Q 功能是必需的。
J Lipid Res. 2019 Jul;60(7):1293-1310. doi: 10.1194/jlr.M093534. Epub 2019 May 2.
9
Secondary CoQ deficiency, bioenergetics unbalance in disease and aging.继发 CoQ 缺乏,疾病和衰老中的生物能量失衡。
Biofactors. 2021 Jul;47(4):551-569. doi: 10.1002/biof.1733. Epub 2021 Apr 20.
10
4-Hydroxybenzoic acid rescues multisystemic disease and perinatal lethality in a mouse model of mitochondrial disease.4- 羟基苯甲酸可挽救线粒体疾病小鼠模型中的多系统疾病和围产期致死性。
Cell Rep. 2024 May 28;43(5):114148. doi: 10.1016/j.celrep.2024.114148. Epub 2024 May 1.

引用本文的文献

1
Ferroptosis in Cancer and Inflammatory Diseases: Mechanisms and Therapeutic Implications.癌症与炎症性疾病中的铁死亡:机制与治疗意义
MedComm (2020). 2025 Sep 3;6(9):e70349. doi: 10.1002/mco2.70349. eCollection 2025 Sep.
2
Profiling with senescence-associated secretory phenotype score identifies GDC-0879 as a small molecule sensitizing glioblastoma to anti-PD1.通过衰老相关分泌表型评分进行分析发现,GDC-0879是一种使胶质母细胞瘤对抗PD1敏感的小分子。
Cell Death Dis. 2025 Aug 9;16(1):602. doi: 10.1038/s41419-025-07915-3.
3
Metabolic reprogramming by endothelial ANGPTL4 depletion protects against diabetic kidney disease.内皮细胞血管生成素样蛋白4缺失引起的代谢重编程可预防糖尿病肾病。
bioRxiv. 2025 May 12:2025.05.08.652142. doi: 10.1101/2025.05.08.652142.
4
Prenyl diphosphate synthase subunit 2 is downregulated in abdominal aortic aneurysm and retards the progression of abdominal aortic aneurysm.异戊二烯二磷酸合酶亚基2在腹主动脉瘤中表达下调,并延缓腹主动脉瘤的进展。
Cytojournal. 2024 Dec 13;21:63. doi: 10.25259/Cytojournal_70_2024. eCollection 2024.
5
Expanding the clinical spectrum of 19p13.3 microduplication syndrome: a case report highlighting nephrotic syndrome and literature review.扩展19p13.3微重复综合征的临床谱:一例突出肾病综合征的病例报告及文献综述
BMC Pediatr. 2025 Jan 28;25(1):70. doi: 10.1186/s12887-025-05394-1.
6
starTracer is an accelerated approach for precise marker gene identification in single-cell RNA-Seq analysis.StarTracer 是一种在单细胞 RNA-Seq 分析中用于精确标记基因识别的加速方法。
Commun Biol. 2024 Sep 13;7(1):1128. doi: 10.1038/s42003-024-06790-6.
7
Mechanisms of Abnormal Lipid Metabolism in the Pathogenesis of Disease.疾病发病机制中的异常脂质代谢机制。
Int J Mol Sci. 2024 Aug 2;25(15):8465. doi: 10.3390/ijms25158465.
8
Organelle communication maintains mitochondrial and endosomal homeostasis during podocyte lipotoxicity.细胞器通讯在足细胞脂肪毒性过程中维持线粒体和内体的平衡。
JCI Insight. 2024 Aug 8;9(18):e182534. doi: 10.1172/jci.insight.182534.
9
Targeting the transmembrane cytokine co-receptor neuropilin-1 in distal tubules improves renal injury and fibrosis.靶向远曲小管的跨膜细胞因子共受体神经纤毛蛋白-1可改善肾损伤和纤维化。
Nat Commun. 2024 Jul 8;15(1):5731. doi: 10.1038/s41467-024-50121-6.
10
Comprehensive analysis of the endothelin system in the kidneys of mice, rats, and humans.全面分析小鼠、大鼠和人类肾脏中的内皮素系统。
Biosci Rep. 2024 Jul 31;44(7). doi: 10.1042/BSR20240768.

本文引用的文献

1
Soluble RARRES1 induces podocyte apoptosis to promote glomerular disease progression.可溶性 RARRES1 诱导足细胞凋亡促进肾小球疾病进展。
J Clin Invest. 2020 Oct 1;130(10):5523-5535. doi: 10.1172/JCI140155.
2
Cell profiling of mouse acute kidney injury reveals conserved cellular responses to injury.小鼠急性肾损伤的细胞分析揭示了损伤后细胞反应的保守性。
Proc Natl Acad Sci U S A. 2020 Jul 7;117(27):15874-15883. doi: 10.1073/pnas.2005477117. Epub 2020 Jun 22.
3
ADCK4 Deficiency Destabilizes the Coenzyme Q Complex, Which Is Rescued by 2,4-Dihydroxybenzoic Acid Treatment.ADCK4 缺乏会使辅酶 Q 复合物不稳定,而 2,4-二羟基苯甲酸处理可挽救这一情况。
J Am Soc Nephrol. 2020 Jun;31(6):1191-1211. doi: 10.1681/ASN.2019070756. Epub 2020 May 7.
4
A Compendium of Genetic Modifiers of Mitochondrial Dysfunction Reveals Intra-organelle Buffering.遗传修饰物综合分析揭示了线粒体功能障碍的细胞器内缓冲作用。
Cell. 2019 Nov 14;179(5):1222-1238.e17. doi: 10.1016/j.cell.2019.10.032.
5
The CoQ oxidoreductase FSP1 acts parallel to GPX4 to inhibit ferroptosis.辅酶 Q 氧化还原酶 FSP1 与 GPX4 平行作用以抑制铁死亡。
Nature. 2019 Nov;575(7784):688-692. doi: 10.1038/s41586-019-1705-2. Epub 2019 Oct 21.
6
FSP1 is a glutathione-independent ferroptosis suppressor.FSP1 是一种谷胱甘肽不依赖的铁死亡抑制因子。
Nature. 2019 Nov;575(7784):693-698. doi: 10.1038/s41586-019-1707-0. Epub 2019 Oct 21.
7
Small Molecule Targets TMED9 and Promotes Lysosomal Degradation to Reverse Proteinopathy.小分子靶向 TMED9 并促进溶酶体降解以逆转蛋白病。
Cell. 2019 Jul 25;178(3):521-535.e23. doi: 10.1016/j.cell.2019.07.002.
8
Anaerobic Glycolysis Maintains the Glomerular Filtration Barrier Independent of Mitochondrial Metabolism and Dynamics.无氧糖酵解独立于线粒体代谢和动力学维持肾小球滤过屏障。
Cell Rep. 2019 Apr 30;27(5):1551-1566.e5. doi: 10.1016/j.celrep.2019.04.012.
9
Novel parietal epithelial cell subpopulations contribute to focal segmental glomerulosclerosis and glomerular tip lesions.新型壁层上皮细胞亚群导致局灶节段性肾小球硬化和肾小球顶尖病变。
Kidney Int. 2019 Jul;96(1):80-93. doi: 10.1016/j.kint.2019.01.037. Epub 2019 Feb 27.
10
MAPK/ERK Signaling in Regulation of Renal Differentiation.MAPK/ERK 信号通路在肾脏分化中的调控作用。
Int J Mol Sci. 2019 Apr 10;20(7):1779. doi: 10.3390/ijms20071779.

靶向 Braf/Mapk 通路可挽救 CoQ 缺乏症肾病中足细胞的脂质过氧化。

Targeting a Braf/Mapk pathway rescues podocyte lipid peroxidation in CoQ-deficiency kidney disease.

机构信息

Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA.

Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.

出版信息

J Clin Invest. 2021 Mar 1;131(5). doi: 10.1172/JCI141380.

DOI:10.1172/JCI141380
PMID:33444290
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7919729/
Abstract

Mutations affecting mitochondrial coenzyme Q (CoQ) biosynthesis lead to kidney failure due to selective loss of podocytes, essential cells of the kidney filter. Curiously, neighboring tubular epithelial cells are spared early in disease despite higher mitochondrial content. We sought to illuminate noncanonical, cell-specific roles for CoQ, independently of the electron transport chain (ETC). Here, we demonstrate that CoQ depletion caused by Pdss2 enzyme deficiency in podocytes results in perturbations in polyunsaturated fatty acid (PUFA) metabolism and the Braf/Mapk pathway rather than ETC dysfunction. Single-nucleus RNA-Seq from kidneys of Pdss2kd/kd mice with nephrotic syndrome and global CoQ deficiency identified a podocyte-specific perturbation of the Braf/Mapk pathway. Treatment with GDC-0879, a Braf/Mapk-targeting compound, ameliorated kidney disease in Pdss2kd/kd mice. Mechanistic studies in Pdss2-depleted podocytes revealed a previously unknown perturbation in PUFA metabolism that was confirmed in vivo. Gpx4, an enzyme that protects against PUFA-mediated lipid peroxidation, was elevated in disease and restored after GDC-0879 treatment. We demonstrate broader human disease relevance by uncovering patterns of GPX4 and Braf/Mapk pathway gene expression in tissue from patients with kidney diseases. Our studies reveal ETC-independent roles for CoQ in podocytes and point to Braf/Mapk as a candidate pathway for the treatment of kidney diseases.

摘要

影响线粒体辅酶 Q(CoQ)生物合成的突变会导致肾脏衰竭,这是由于足细胞的选择性丧失,足细胞是肾脏过滤的重要细胞。奇怪的是,尽管线粒体含量较高,但在疾病早期,相邻的肾小管上皮细胞却幸免于难。我们试图阐明 CoQ 的非典型、细胞特异性作用,而不依赖于电子传递链(ETC)。在这里,我们证明了由于 Pdss2 酶在足细胞中的缺陷导致 CoQ 耗竭,会导致多不饱和脂肪酸(PUFA)代谢和 Braf/Mapk 途径的紊乱,而不是 ETC 功能障碍。患有肾病综合征和全身 CoQ 缺乏症的 Pdss2kd/kd 小鼠肾脏的单核 RNA-Seq 鉴定出足细胞中 Braf/Mapk 途径的特定扰动。用 GDC-0879(一种靶向 Braf/Mapk 的化合物)治疗可改善 Pdss2kd/kd 小鼠的肾脏疾病。在 Pdss2 耗尽的足细胞中的机制研究揭示了先前未知的 PUFA 代谢紊乱,在体内得到了证实。Gpx4 是一种可防止 PUFA 介导的脂质过氧化的酶,在疾病中升高,并在 GDC-0879 治疗后恢复。通过揭示组织中 GPX4 和 Braf/Mapk 途径基因表达的模式,我们证明了 CoQ 在足细胞中具有更广泛的人类疾病相关性。我们的研究揭示了 CoQ 在足细胞中独立于 ETC 的作用,并指出 Braf/Mapk 是治疗肾脏疾病的候选途径。