• 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

肾脏疾病中的鞘脂信号传导

Sphingolipid signaling in kidney diseases.

作者信息

Li Ningjun, Li Guangbi

机构信息

Department of Pharmacology and Toxicology, School of Medicine, Virginia Commonwealth University, Richmond, Virginia, United States.

出版信息

Am J Physiol Renal Physiol. 2025 Mar 1;328(3):F431-F443. doi: 10.1152/ajprenal.00193.2024. Epub 2025 Feb 11.

DOI:10.1152/ajprenal.00193.2024
PMID:39933715
Abstract

Sphingolipids are a family of bioactive lipids. The key components include ceramides, ceramide-1-phosphate, sphingosine, and sphingosine-1-phosphate. Sphingolipids were originally considered to be primarily structural elements of cell membranes but were later recognized as bioactive signaling molecules that play diverse roles in cellular behaviors such as cell differentiation, migration, proliferation, and death. Studies have demonstrated changes in key components of sphingolipids in the kidneys under different conditions and their important roles in the renal function and the pathogenesis of various kidney diseases. This review summarizes the most recent advances in the role of sphingolipid signaling in kidney diseases.

摘要

鞘脂是一类生物活性脂质。其关键成分包括神经酰胺、神经酰胺-1-磷酸、鞘氨醇和鞘氨醇-1-磷酸。鞘脂最初被认为主要是细胞膜的结构成分,但后来被确认为生物活性信号分子,在细胞分化、迁移、增殖和死亡等细胞行为中发挥多种作用。研究表明,在不同条件下肾脏中鞘脂的关键成分会发生变化,它们在肾功能和各种肾脏疾病的发病机制中具有重要作用。本综述总结了鞘脂信号在肾脏疾病中作用的最新进展。

相似文献

1
Sphingolipid signaling in kidney diseases.肾脏疾病中的鞘脂信号传导
Am J Physiol Renal Physiol. 2025 Mar 1;328(3):F431-F443. doi: 10.1152/ajprenal.00193.2024. Epub 2025 Feb 11.
2
Sphingosine-1-Phosphate Metabolism and Signaling in Kidney Diseases.鞘氨醇-1-磷酸代谢与肾脏病信号通路
J Am Soc Nephrol. 2021 Jan;32(1):9-31. doi: 10.1681/ASN.2020050697. Epub 2020 Dec 18.
3
Metabolism and biological functions of two phosphorylated sphingolipids, sphingosine 1-phosphate and ceramide 1-phosphate.两种磷酸化鞘脂——1-磷酸鞘氨醇和1-磷酸神经酰胺的代谢及生物学功能
Prog Lipid Res. 2007 Mar;46(2):126-44. doi: 10.1016/j.plipres.2007.03.001. Epub 2007 Mar 14.
4
Impact of Sphingolipid Mediators on the Determination of Cochlear Survival in Ototoxicity.鞘脂介质对耳毒性中耳蜗存活判定的影响
Curr Mol Pharmacol. 2018;11(4):279-284. doi: 10.2174/1874467211666180516101111.
5
Control of metabolism and signaling of simple bioactive sphingolipids: Implications in disease.简单生物活性神经酰胺代谢和信号转导的控制:疾病的影响。
Prog Lipid Res. 2010 Oct;49(4):316-34. doi: 10.1016/j.plipres.2010.02.004. Epub 2010 Mar 1.
6
Sphingolipids and cancer: ceramide and sphingosine-1-phosphate in the regulation of cell death and drug resistance.鞘脂类和癌症:细胞死亡和耐药性调控中的神经酰胺和 1-磷酸鞘氨醇。
Future Oncol. 2010 Oct;6(10):1603-24. doi: 10.2217/fon.10.116.
7
[The role of sphingolipids in selected cardiovascular diseases].[鞘脂类在特定心血管疾病中的作用]
Postepy Hig Med Dosw (Online). 2013 Sep 30;67:1018-26. doi: 10.5604/17322693.1068694.
8
Differential effects of ceramide and sphingosine 1-phosphate on ERM phosphorylation: probing sphingolipid signaling at the outer plasma membrane.神经鞘氨醇 1-磷酸和神经酰胺对 ERM 磷酸化的差异影响:在外质膜探测鞘脂信号。
J Biol Chem. 2010 Oct 15;285(42):32476-85. doi: 10.1074/jbc.M110.141028. Epub 2010 Aug 2.
9
Characterization of ceramide synthase 2: tissue distribution, substrate specificity, and inhibition by sphingosine 1-phosphate.神经酰胺合成酶2的特性:组织分布、底物特异性以及受1-磷酸鞘氨醇的抑制作用
J Biol Chem. 2008 Feb 29;283(9):5677-84. doi: 10.1074/jbc.M707386200. Epub 2007 Dec 28.
10
Sphingolipids in mammalian cell signalling.哺乳动物细胞信号传导中的鞘脂类
Cell Mol Life Sci. 2001 Dec;58(14):2053-68. doi: 10.1007/PL00000836.

本文引用的文献

1
Epigenetics of Homocystinuria, Hydrogen Sulfide, and Circadian Clock Ablation in Cardiovascular-Renal Disease.心血管-肾脏疾病中高同型半胱氨酸尿症、硫化氢与昼夜节律钟缺失的表观遗传学
Curr Issues Mol Biol. 2024 Dec 5;46(12):13783-13797. doi: 10.3390/cimb46120824.
2
Podocyte-specific silencing of acid sphingomyelinase gene to abrogate hyperhomocysteinemia-induced NLRP3 inflammasome activation and glomerular inflammation.足细胞特异性沉默酸性鞘磷脂酶基因以消除高同型半胱氨酸血症诱导的NLRP3炎性小体激活和肾小球炎症。
Am J Physiol Renal Physiol. 2024 Jun 1;326(6):F988-F1003. doi: 10.1152/ajprenal.00195.2023. Epub 2024 Apr 18.
3
Sphingosine 1-Phosphate Regulates Obesity and Glucose Homeostasis.
鞘氨醇 1-磷酸调节肥胖和葡萄糖稳态。
Int J Mol Sci. 2024 Jan 11;25(2):932. doi: 10.3390/ijms25020932.
4
Urinary sphingolipids in adolescents and young adults with youth-onset diabetes.青少年和青年起病糖尿病患者的尿鞘氨醇脂质。
Pediatr Nephrol. 2024 Jun;39(6):1875-1883. doi: 10.1007/s00467-023-06257-6. Epub 2024 Jan 3.
5
Expression of Ceramide Synthases in Mice and Their Roles in Regulating Acyl-Chain Sphingolipids: A Framework for Baseline Levels and Future Implications in Aging and Disease.鞘氨醇合酶在小鼠中的表达及其对酰基鞘氨醇脂质调节的作用:衰老和疾病中基线水平及未来意义的框架。
Mol Pharmacol. 2024 Feb 15;105(3):131-143. doi: 10.1124/molpharm.123.000788.
6
Immunolocalization of Sphingolipid Catabolism Enzymes along the Nephron: Novel Early Urinary Biomarkers of Renal Damage.沿肾单位的鞘脂分解代谢酶的免疫定位:肾脏损伤的新型早期尿生物标志物。
Int J Mol Sci. 2023 Nov 23;24(23):16633. doi: 10.3390/ijms242316633.
7
The therapeutic potential of sphingolipids for cardiovascular diseases.鞘脂类对心血管疾病的治疗潜力。
Front Cardiovasc Med. 2023 Aug 7;10:1224743. doi: 10.3389/fcvm.2023.1224743. eCollection 2023.
8
Regulation of NLRP3 Inflammasome Activation and Inflammatory Exosome Release in Podocytes by Acid Sphingomyelinase During Obesity.肥胖时酸性鞘磷脂酶调节足细胞 NLRP3 炎性小体激活和炎症外泌体释放。
Inflammation. 2023 Oct;46(5):2037-2054. doi: 10.1007/s10753-023-01861-y. Epub 2023 Jul 21.
9
CERS6-derived ceramides aggravate kidney fibrosis by inhibiting PINK1-mediated mitophagy in diabetic kidney disease.CERS6 衍生的神经酰胺通过抑制 PINK1 介导的糖尿病肾病中的细胞自噬加剧肾脏纤维化。
Am J Physiol Cell Physiol. 2023 Aug 1;325(2):C538-C549. doi: 10.1152/ajpcell.00144.2023. Epub 2023 Jul 17.
10
Ceramide in cerebrovascular diseases.脑血管疾病中的神经酰胺
Front Cell Neurosci. 2023 Jun 2;17:1191609. doi: 10.3389/fncel.2023.1191609. eCollection 2023.