• 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

Pax6对于晚期生成的视网膜神经元的产生以及在视网膜发育后期抑制光感受器命运至关重要。

Pax6 is essential for the generation of late-born retinal neurons and for inhibition of photoreceptor-fate during late stages of retinogenesis.

作者信息

Remez Liv Aleen, Onishi Akishi, Menuchin-Lasowski Yotam, Biran Assaf, Blackshaw Seth, Wahlin Karl J, Zack Donlad J, Ashery-Padan Ruth

机构信息

Department of Human Molecular Genetics and Biochemistry, Faculty of Medicine and Sagol School of Neuroscience, Tel-Aviv University, Tel Aviv, Israel.

Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.

出版信息

Dev Biol. 2017 Dec 1;432(1):140-150. doi: 10.1016/j.ydbio.2017.09.030. Epub 2017 Oct 7.

DOI:10.1016/j.ydbio.2017.09.030
PMID:28993200
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5882491/
Abstract

In the developing retina, as in other regions of the CNS, neural progenitors give rise to individual cell types during discrete temporal windows. Pax6 is expressed in retinal progenitor cells (RPCs) throughout the course of retinogenesis, and has been shown to be required during early retinogenesis for generation of most early-born cell types. In this study, we examined the function of Pax6 in postnatal mouse retinal development. We found that Pax6 is essential for the generation of late-born interneurons, while inhibiting photoreceptor differentiation. Generation of bipolar interneurons requires Pax6 expression in RPCs, while Pax6 is required for the generation of glycinergic, but not for GABAergic or non-GABAergic-non-glycinergic (nGnG) amacrine cell subtypes. In contrast, overexpression of either full-length Pax6 or its 5a isoform in RPCs induces formation of cells with nGnG amacrine features, and suppresses generation of other inner retinal cell types. Moreover, overexpression of both Pax6 variants prevents photoreceptor differentiation, most likely by inhibiting Crx expression. Taken together, these data show that Pax6 acts in RPCs to control differentiation of multiple late-born neuronal cell types.

摘要

在发育中的视网膜中,与中枢神经系统的其他区域一样,神经祖细胞在离散的时间窗口内产生不同的细胞类型。在整个视网膜发生过程中,Pax6在视网膜祖细胞(RPCs)中表达,并且已表明在早期视网膜发生过程中,Pax6是生成大多数早期产生的细胞类型所必需的。在本研究中,我们研究了Pax6在出生后小鼠视网膜发育中的功能。我们发现,Pax6对于晚期产生的中间神经元的生成至关重要,同时抑制光感受器分化。双极中间神经元的生成需要RPCs中Pax6的表达,而甘氨酸能无长突细胞亚型的生成需要Pax6,但GABA能或非GABA能 - 非甘氨酸能(nGnG)无长突细胞亚型的生成则不需要Pax6。相反,在RPCs中全长Pax6或其5a亚型的过表达会诱导形成具有nGnG无长突细胞特征的细胞,并抑制其他视网膜内层细胞类型的生成。此外,两种Pax6变体的过表达很可能通过抑制Crx表达来阻止光感受器分化。综上所述,这些数据表明Pax6在RPCs中发挥作用,以控制多种晚期产生的神经元细胞类型的分化。

相似文献

1
Pax6 is essential for the generation of late-born retinal neurons and for inhibition of photoreceptor-fate during late stages of retinogenesis.Pax6对于晚期生成的视网膜神经元的产生以及在视网膜发育后期抑制光感受器命运至关重要。
Dev Biol. 2017 Dec 1;432(1):140-150. doi: 10.1016/j.ydbio.2017.09.030. Epub 2017 Oct 7.
2
Dual requirement for Pax6 in retinal progenitor cells.视网膜祖细胞中Pax6的双重需求。
Development. 2008 Dec;135(24):4037-4047. doi: 10.1242/dev.028308. Epub 2008 Nov 12.
3
Gene expression is dynamically regulated in retinal progenitor cells prior to and during overt cellular differentiation.在明显的细胞分化之前及分化过程中,视网膜祖细胞中的基因表达受到动态调控。
Gene Expr Patterns. 2014 Jan;14(1):42-54. doi: 10.1016/j.gep.2013.10.003. Epub 2013 Oct 19.
4
Dlx1, Dlx2, Pax6, Brn3b, and Chx10 homeobox gene expression defines the retinal ganglion and inner nuclear layers of the developing and adult mouse retina.Dlx1、Dlx2、Pax6、Brn3b和Chx10同源框基因的表达界定了发育中和成年小鼠视网膜的视网膜神经节细胞层和内核层。
J Comp Neurol. 2003 Jun 23;461(2):187-204. doi: 10.1002/cne.10674.
5
Docosahexaenoic acid promotes photoreceptor differentiation without altering Crx expression.二十二碳六烯酸可促进光感受器分化,而不改变Crx的表达。
Invest Ophthalmol Vis Sci. 2006 Jul;47(7):3017-27. doi: 10.1167/iovs.05-1659.
6
Involvement of Bcl-2-associated transcription factor 1 in the differentiation of early-born retinal cells.Bcl-2 相关转录因子 1 参与早期出生的视网膜细胞的分化。
J Neurosci. 2014 Jan 22;34(4):1530-41. doi: 10.1523/JNEUROSCI.3227-13.2014.
7
Sip1 regulates the generation of the inner nuclear layer retinal cell lineages in mammals.Sip1调节哺乳动物内核层视网膜细胞谱系的生成。
Development. 2016 Aug 1;143(15):2829-41. doi: 10.1242/dev.136101. Epub 2016 Jul 6.
8
Krüppel-Like Factor 4 (KLF4) Is Not Required for Retinal Cell Differentiation.Krüppel 样因子 4(KLF4)对于视网膜细胞分化并非必需。
eNeuro. 2016 Feb 27;3(1). doi: 10.1523/ENEURO.0117-15.2016. eCollection 2016 Jan-Feb.
9
Pax6 is required for the multipotent state of retinal progenitor cells.视网膜祖细胞的多能状态需要Pax6。
Cell. 2001 Apr 6;105(1):43-55. doi: 10.1016/s0092-8674(01)00295-1.
10
Foxn4 is a temporal identity factor conferring mid/late-early retinal competence and involved in retinal synaptogenesis.Foxn4 是一个赋予视网膜中晚期早期状态的时间特征性因子,并参与视网膜突触发生。
Proc Natl Acad Sci U S A. 2020 Mar 3;117(9):5016-5027. doi: 10.1073/pnas.1918628117. Epub 2020 Feb 18.

引用本文的文献

1
The Chronological Trigger: The Orchestra Between Homeobox Genes and the Circadian Clock During Development.时间触发因素:发育过程中同源异型基因与生物钟之间的协调作用
Biol Cell. 2025 Jul;117(7):e70027. doi: 10.1111/boc.70027.
2
Massively parallel reporter assay for mapping gene-specific regulatory regions at single nucleotide resolution.用于在单核苷酸分辨率下绘制基因特异性调控区域的大规模平行报告基因检测法。
bioRxiv. 2025 May 14:2025.05.13.653746. doi: 10.1101/2025.05.13.653746.
3
Excluding the Genomic Location of Pax2 Regulatory Elements for the Developing Mouse Eye.

本文引用的文献

1
Tfap2a and 2b act downstream of Ptf1a to promote amacrine cell differentiation during retinogenesis.Tfap2a和2b在视网膜生成过程中于Ptf1a下游发挥作用,以促进无长突细胞分化。
Mol Brain. 2015 May 13;8:28. doi: 10.1186/s13041-015-0118-x.
2
Regulation of cerebral cortical neurogenesis by the Pax6 transcription factor.Pax6 转录因子对大脑皮质神经发生的调控。
Front Cell Neurosci. 2015 Mar 10;9:70. doi: 10.3389/fncel.2015.00070. eCollection 2015.
3
The cellular and molecular mechanisms of vertebrate lens development.脊椎动物晶状体发育的细胞和分子机制。
排除发育中小鼠眼睛的Pax2调控元件的基因组位置。
Genesis. 2025 Apr;63(2):e70016. doi: 10.1002/dvg.70016.
4
Rapid and efficient generation of mature retinal organoids derived from human pluripotent stem cells via optimized pharmacological modulation of Sonic hedgehog, activin A, and retinoic acid signal transduction.通过优化 Sonic hedgehog、激活素 A 和视黄酸信号转导的药理学调节,从人多能干细胞快速有效地生成成熟的视网膜类器官。
PLoS One. 2024 Aug 9;19(8):e0308743. doi: 10.1371/journal.pone.0308743. eCollection 2024.
5
Repurposing development genes for axonal regeneration following injury: Examining the roles of Wnt signaling.重新利用发育基因促进损伤后的轴突再生:探究Wnt信号通路的作用。
Front Cell Dev Biol. 2024 May 31;12:1417928. doi: 10.3389/fcell.2024.1417928. eCollection 2024.
6
Stage-specific dynamic reorganization of genome topology shapes transcriptional neighborhoods in developing human retinal organoids.特定发育阶段的基因组拓扑结构动态重排塑造了人视网膜类器官中的转录邻域。
Cell Rep. 2023 Dec 26;42(12):113543. doi: 10.1016/j.celrep.2023.113543. Epub 2023 Dec 3.
7
Integrated multi-omics single cell atlas of the human retina.人类视网膜的综合多组学单细胞图谱。
Res Sq. 2023 Nov 17:rs.3.rs-3471275. doi: 10.21203/rs.3.rs-3471275/v1.
8
Characterization of neural damage and neuroinflammation in Pax6 small-eye mice.Pax6 小眼球小鼠的神经损伤和神经炎症特征。
Exp Eye Res. 2024 Jan;238:109723. doi: 10.1016/j.exer.2023.109723. Epub 2023 Nov 16.
9
Unique activities of two overlapping retinal enhancers.两个重叠视网膜增强子的独特活性。
Life Sci Alliance. 2023 Aug 29;6(11). doi: 10.26508/lsa.202302126. Print 2023 Nov.
10
Molecular mechanisms controlling vertebrate retinal patterning, neurogenesis, and cell fate specification.控制脊椎动物视网膜模式形成、神经发生和细胞命运特化的分子机制。
Trends Genet. 2023 Oct;39(10):736-757. doi: 10.1016/j.tig.2023.06.002. Epub 2023 Jul 8.
Development. 2014 Dec;141(23):4432-47. doi: 10.1242/dev.107953. Epub 2014 Nov 18.
4
A gene regulatory network controls the binary fate decision of rod and bipolar cells in the vertebrate retina.一个基因调控网络控制着脊椎动物视网膜中杆状细胞和双极细胞的二元命运决定。
Dev Cell. 2014 Sep 8;30(5):513-27. doi: 10.1016/j.devcel.2014.07.018. Epub 2014 Aug 21.
5
Intrinsically different retinal progenitor cells produce specific types of progeny.内在不同的视网膜祖细胞产生特定类型的后代。
Nat Rev Neurosci. 2014 Sep;15(9):615-27. doi: 10.1038/nrn3767. Epub 2014 Aug 6.
6
PAX6 regulates melanogenesis in the retinal pigmented epithelium through feed-forward regulatory interactions with MITF.PAX6 通过与 MITF 的前馈调节相互作用来调控视网膜色素上皮中的黑色素生成。
PLoS Genet. 2014 May 29;10(5):e1004360. doi: 10.1371/journal.pgen.1004360. eCollection 2014.
7
Stage-dependent requirement of neuroretinal Pax6 for lens and retina development.神经视网膜 Pax6 对晶状体和视网膜发育的阶段依赖性需求。
Development. 2014 Mar;141(6):1292-302. doi: 10.1242/dev.098822. Epub 2014 Feb 12.
8
Pax6 is required for normal cell-cycle exit and the differentiation kinetics of retinal progenitor cells.Pax6 对于视网膜祖细胞的正常细胞周期退出和分化动力学是必需的。
PLoS One. 2013 Sep 20;8(9):e76489. doi: 10.1371/journal.pone.0076489. eCollection 2013.
9
An isoform of retinoid-related orphan receptor β directs differentiation of retinal amacrine and horizontal interneurons.视黄酸相关孤儿受体 β 的一种异构体指导视网膜无长突细胞和水平中间神经元的分化。
Nat Commun. 2013;4:1813. doi: 10.1038/ncomms2793.
10
Functional dissection of the paired domain of Pax6 reveals molecular mechanisms of coordinating neurogenesis and proliferation.Pax6 二聚结构域的功能解析揭示了协调神经发生和增殖的分子机制。
Development. 2013 Mar;140(5):1123-36. doi: 10.1242/dev.082875.