• 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

PKG 依赖性细胞死亡在 661W 视锥细胞样细胞培养物中的作用(实验研究)。

PKG-Dependent Cell Death in 661W Cone Photoreceptor-like Cell Cultures (Experimental Study).

机构信息

University Hospital Essen, Department of Neurology, Essen, Germany.

Department für Augenheilkunde, Forschungsinstitut für Augenheilkunde, Eberhard Karls Universität Tübingen, Tübingen, Germany.

出版信息

Adv Exp Med Biol. 2018;1074:511-517. doi: 10.1007/978-3-319-75402-4_63.

DOI:10.1007/978-3-319-75402-4_63
PMID:29721983
Abstract

In humans cone photoreceptors are responsible for high-resolution colour vision. A variety of retinal diseases can compromise cone viability, and, at present, no satisfactory treatment options are available. Here, we present data towards establishing a reliable, high-throughput assay system that will facilitate the search for cone neuroprotective compounds using the murine-photoreceptor cell line 661 W. To further characterize 661 W cells, a retinal marker study was performed, followed by the induction of cell death using paradigms over-activating cGMP-dependent protein kinase G (PKG). We found that 661 W cells may be used to mimic specific aspects of cone degeneration and may thus be valuable for future compound screening studies.

摘要

在人类中,视锥细胞负责高分辨率的色彩视觉。多种视网膜疾病会损害视锥细胞的活力,而目前尚无可令人满意的治疗方法。在这里,我们提出了建立可靠的高通量检测系统的数据,这将有助于使用小鼠感光细胞系 661W 寻找视锥细胞神经保护化合物。为了进一步描述 661W 细胞,我们进行了视网膜标志物研究,然后使用过度激活 cGMP 依赖性蛋白激酶 G(PKG)的范例诱导细胞死亡。我们发现,661W 细胞可用于模拟视锥细胞退化的特定方面,因此对未来的化合物筛选研究可能具有重要价值。

相似文献

1
PKG-Dependent Cell Death in 661W Cone Photoreceptor-like Cell Cultures (Experimental Study).PKG 依赖性细胞死亡在 661W 视锥细胞样细胞培养物中的作用(实验研究)。
Adv Exp Med Biol. 2018;1074:511-517. doi: 10.1007/978-3-319-75402-4_63.
2
cGMP/Protein Kinase G Signaling Suppresses Inositol 1,4,5-Trisphosphate Receptor Phosphorylation and Promotes Endoplasmic Reticulum Stress in Photoreceptors of Cyclic Nucleotide-gated Channel-deficient Mice.环磷酸鸟苷/蛋白激酶G信号传导抑制1,4,5-三磷酸肌醇受体磷酸化并促进环核苷酸门控通道缺陷小鼠光感受器中的内质网应激。
J Biol Chem. 2015 Aug 21;290(34):20880-20892. doi: 10.1074/jbc.M115.641159. Epub 2015 Jun 29.
3
Potential contribution of ryanodine receptor 2 upregulation to cGMP/PKG signaling-induced cone degeneration in cyclic nucleotide-gated channel deficiency.钙释放激活钙通道(ryanodine receptor 2,RyR2)功能上调在环核苷酸门控通道缺陷所致的视锥细胞变性中的潜在作用
FASEB J. 2020 May;34(5):6335-6350. doi: 10.1096/fj.201901951RR. Epub 2020 Mar 16.
4
cGMP-dependent cone photoreceptor degeneration in the cpfl1 mouse retina.cpfl1 小鼠视网膜中环鸟苷酸依赖性视锥细胞光感受器变性。
J Comp Neurol. 2010 Sep 1;518(17):3604-17. doi: 10.1002/cne.22416.
5
Phosphodiesterase inhibition induces retinal degeneration, oxidative stress and inflammation in cone-enriched cultures of porcine retina.磷酸二酯酶抑制导致富含锥体的猪视网膜培养物发生视网膜变性、氧化应激和炎症。
Exp Eye Res. 2013 Jun;111:122-33. doi: 10.1016/j.exer.2013.03.015. Epub 2013 Apr 9.
6
Two pathways of rod photoreceptor cell death induced by elevated cGMP.由升高的环鸟苷酸诱导的视杆光感受器细胞死亡的两条途径。
Hum Mol Genet. 2017 Jun 15;26(12):2299-2306. doi: 10.1093/hmg/ddx121.
7
Cone neurite sprouting: an early onset abnormality of the cone photoreceptors in the retinal degeneration mouse.视锥神经突萌发:视网膜变性小鼠中视锥光感受器的早期异常。
Mol Vis. 2002 Aug 27;8:306-14.
8
Do cGMP Levels Drive the Speed of Photoreceptor Degeneration?环鸟苷酸水平是否影响光感受器变性速度?
Adv Exp Med Biol. 2018;1074:327-333. doi: 10.1007/978-3-319-75402-4_40.
9
Feedback control through cGMP-dependent protein kinase contributes to differential regulation and compartmentation of cGMP in rat cardiac myocytes.通过 cGMP 依赖性蛋白激酶的反馈控制有助于调节和区室化大鼠心肌细胞中的 cGMP。
Circ Res. 2010 Nov 12;107(10):1232-40. doi: 10.1161/CIRCRESAHA.110.226712. Epub 2010 Sep 16.
10
The bradykinin-cGMP-PKG pathway augments insulin sensitivity via upregulation of MAPK phosphatase-5 and inhibition of JNK.缓激肽 - 环磷酸鸟苷 - 蛋白激酶G途径通过上调丝裂原活化蛋白激酶磷酸酶 - 5和抑制应激活化蛋白激酶来增强胰岛素敏感性。
Am J Physiol Endocrinol Metab. 2017 Sep 1;313(3):E321-E334. doi: 10.1152/ajpendo.00298.2016. Epub 2017 Jul 5.

引用本文的文献

1
A review of the 661W cell line as a tool to facilitate treatment development for retinal diseases.661W细胞系作为促进视网膜疾病治疗发展工具的综述。
Cell Biosci. 2025 Apr 1;15(1):41. doi: 10.1186/s13578-025-01381-2.
2
Evaluation of mesenchymal stem cells as an model for inherited retinal diseases.间充质干细胞作为遗传性视网膜疾病模型的评估。
Front Cell Dev Biol. 2024 Nov 15;12:1455140. doi: 10.3389/fcell.2024.1455140. eCollection 2024.
3
Single-Cell Transcriptomic Profiling in Inherited Retinal Degeneration Reveals Distinct Metabolic Pathways in Rod and Cone Photoreceptors.
单细胞转录组分析揭示遗传性视网膜变性中杆状和锥状光感受器的不同代谢途径。
Int J Mol Sci. 2022 Oct 12;23(20):12170. doi: 10.3390/ijms232012170.
4
Model Systems for Studies Into Retinal Neuroprotection.视网膜神经保护研究的模型系统
Front Neurosci. 2022 Jul 7;16:938089. doi: 10.3389/fnins.2022.938089. eCollection 2022.
5
Programmed Non-Apoptotic Cell Death in Hereditary Retinal Degeneration: Crosstalk between cGMP-Dependent Pathways and PARthanatos?遗传性视网膜变性中的程序性非细胞凋亡性细胞死亡:cGMP 依赖性途径与 PARthanatos 的串扰?
Int J Mol Sci. 2021 Sep 29;22(19):10567. doi: 10.3390/ijms221910567.
6
Identification of Novel Substrates for cGMP Dependent Protein Kinase (PKG) through Kinase Activity Profiling to Understand Its Putative Role in Inherited Retinal Degeneration.通过激酶活性分析鉴定 cGMP 依赖性蛋白激酶 (PKG) 的新型底物,以了解其在遗传性视网膜变性中的潜在作用。
Int J Mol Sci. 2021 Jan 25;22(3):1180. doi: 10.3390/ijms22031180.
7
Microfluidic and Microscale Assays to Examine Regenerative Strategies in the Neuro Retina.用于研究神经视网膜再生策略的微流控和微尺度分析
Micromachines (Basel). 2020 Dec 9;11(12):1089. doi: 10.3390/mi11121089.