• 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

硬骨鱼与类器官:洞察健康与患病大脑发育的新窗口

Teleost Fish and Organoids: Alternative Windows Into the Development of Healthy and Diseased Brains.

作者信息

Fasano Giulia, Compagnucci Claudia, Dallapiccola Bruno, Tartaglia Marco, Lauri Antonella

机构信息

Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Rome, Italy.

出版信息

Front Mol Neurosci. 2022 Aug 11;15:855786. doi: 10.3389/fnmol.2022.855786. eCollection 2022.

DOI:10.3389/fnmol.2022.855786
PMID:36034498
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9403253/
Abstract

The variety in the display of animals' cognition, emotions, and behaviors, typical of humans, has its roots within the anterior-most part of the brain: the forebrain, giving rise to the neocortex in mammals. Our understanding of cellular and molecular events instructing the development of this domain and its multiple adaptations within the vertebrate lineage has progressed in the last decade. Expanding and detailing the available knowledge on regionalization, progenitors' behavior and functional sophistication of the forebrain derivatives is also key to generating informative models to improve our characterization of heterogeneous and mechanistically unexplored cortical malformations. Classical and emerging mammalian models are irreplaceable to accurately elucidate mechanisms of stem cells expansion and impairments of cortex development. Nevertheless, alternative systems, allowing a considerable reduction of the burden associated with animal experimentation, are gaining popularity to dissect basic strategies of neural stem cells biology and morphogenesis in health and disease and to speed up preclinical drug testing. Teleost vertebrates such as zebrafish, showing conserved core programs of forebrain development, together with patients-derived 2D and 3D models, recapitulating more accurately human neurogenesis, are now accepted within translational workflows spanning from genetic analysis to functional investigation. Here, we review the current knowledge of common and divergent mechanisms shaping the forebrain in vertebrates, and causing cortical malformations in humans. We next address the utility, benefits and limitations of whole-brain/organism-based fish models or neuronal ensembles for translational research to unravel key genes and pathological mechanisms involved in neurodevelopmental diseases.

摘要

动物认知、情感和行为表现的多样性,这在人类中很典型,其根源在于大脑最前端的部分:前脑,它在哺乳动物中产生新皮质。在过去十年里,我们对指导该区域发育及其在脊椎动物谱系中多种适应性的细胞和分子事件的理解有了进展。扩展和详述有关前脑衍生物的区域化、祖细胞行为和功能复杂性的现有知识,也是生成信息模型以改善我们对异质性且机制未明的皮质畸形的特征描述的关键。经典和新兴的哺乳动物模型对于准确阐明干细胞扩增机制和皮质发育障碍是不可替代的。然而,能够大幅减轻与动物实验相关负担的替代系统,正越来越受欢迎,用于剖析健康和疾病状态下神经干细胞生物学和形态发生的基本策略,并加速临床前药物测试。硬骨鱼类,如斑马鱼,展示出前脑发育的保守核心程序,连同源自患者的二维和三维模型,能更准确地重现人类神经发生,现在已被纳入从基因分析到功能研究的转化工作流程中。在这里,我们综述了当前关于塑造脊椎动物前脑并导致人类皮质畸形的共同和不同机制的知识。接下来,我们探讨基于全脑/生物体的鱼类模型或神经元集合在转化研究中的效用、益处和局限性,以揭示神经发育疾病中涉及的关键基因和病理机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/570e/9403253/79df6ae30edb/fnmol-15-855786-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/570e/9403253/79df6ae30edb/fnmol-15-855786-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/570e/9403253/79df6ae30edb/fnmol-15-855786-g001.jpg

相似文献

1
Teleost Fish and Organoids: Alternative Windows Into the Development of Healthy and Diseased Brains.硬骨鱼与类器官:洞察健康与患病大脑发育的新窗口
Front Mol Neurosci. 2022 Aug 11;15:855786. doi: 10.3389/fnmol.2022.855786. eCollection 2022.
2
Experimental models of human cortical malformations: from mammals to 'acortical' zebrafish.人类皮质畸形的实验模型:从哺乳动物到“无皮质”斑马鱼
Neurosci Biobehav Rev. 2023 Dec;155:105429. doi: 10.1016/j.neubiorev.2023.105429. Epub 2023 Oct 18.
3
Identification of the optic recess region as a morphogenetic entity in the zebrafish forebrain.将斑马鱼前脑中视隐窝区域鉴定为一个形态发生实体。
Sci Rep. 2015 Mar 4;5:8738. doi: 10.1038/srep08738.
4
Roots of the Malformations of Cortical Development in the Cell Biology of Neural Progenitor Cells.神经祖细胞细胞生物学中皮质发育畸形的根源
Front Neurosci. 2022 Jan 5;15:817218. doi: 10.3389/fnins.2021.817218. eCollection 2021.
5
Modeling Rett Syndrome With Human Patient-Specific Forebrain Organoids.利用人类患者特异性前脑类器官建立雷特综合征模型。
Front Cell Dev Biol. 2020 Dec 10;8:610427. doi: 10.3389/fcell.2020.610427. eCollection 2020.
6
Developmental mechanisms and experimental models to understand forebrain malformative diseases.用于理解前脑畸形疾病的发育机制和实验模型
Genes Brain Behav. 2007 Jun;6 Suppl 1:45-52. doi: 10.1111/j.1601-183X.2007.00322.x.
7
A fully automated high-throughput workflow for 3D-based chemical screening in human midbrain organoids.一种全自动高通量工作流程,用于基于 3D 的人类中脑细胞类器官中的化学筛选。
Elife. 2020 Nov 3;9:e52904. doi: 10.7554/eLife.52904.
8
From Human Pluripotent Stem Cells to Cortical Circuits.从人类多能干细胞到皮质回路。
Curr Top Dev Biol. 2018;129:67-98. doi: 10.1016/bs.ctdb.2018.02.011. Epub 2018 May 9.
9
Cerebral organoids to unravel the mechanisms underlying malformations of human cortical development.脑类器官用于揭示人类皮质发育畸形背后的机制。
Semin Cell Dev Biol. 2021 Mar;111:15-22. doi: 10.1016/j.semcdb.2020.06.001. Epub 2020 Jul 31.
10
Research models of neurodevelopmental disorders: The right model in the right place.神经发育障碍的研究模型:在正确的位置选择正确的模型。
Front Neurosci. 2022 Oct 20;16:1031075. doi: 10.3389/fnins.2022.1031075. eCollection 2022.

引用本文的文献

1
Dominant ARF3 variants disrupt Golgi integrity and cause a neurodevelopmental disorder recapitulated in zebrafish.优势 ARF3 变异破坏高尔基体完整性,并导致斑马鱼中重现的神经发育障碍。
Nat Commun. 2022 Nov 11;13(1):6841. doi: 10.1038/s41467-022-34354-x.

本文引用的文献

1
In-vitro engineered human cerebral tissues mimic pathological circuit disturbances in 3D.体外工程化人类脑组织在三维空间中模拟病理电路紊乱。
Commun Biol. 2022 Mar 23;5(1):254. doi: 10.1038/s42003-022-03203-4.
2
Region Specific Brain Organoids to Study Neurodevelopmental Disorders.用于研究神经发育障碍的区域特异性脑类器官
Int J Stem Cells. 2022 Feb 28;15(1):26-40. doi: 10.15283/ijsc22006.
3
Autism genes converge on asynchronous development of shared neuron classes.自闭症基因集中于共享神经元类别的异步发育。
Nature. 2022 Feb;602(7896):268-273. doi: 10.1038/s41586-021-04358-6. Epub 2022 Feb 2.
4
Deep-Tissue Three-Photon Fluorescence Microscopy in Intact Mouse and Zebrafish Brain.在完整的小鼠和斑马鱼脑组织中进行的深层三光子荧光显微镜技术
J Vis Exp. 2022 Jan 13(179). doi: 10.3791/63213.
5
Roots of the Malformations of Cortical Development in the Cell Biology of Neural Progenitor Cells.神经祖细胞细胞生物学中皮质发育畸形的根源
Front Neurosci. 2022 Jan 5;15:817218. doi: 10.3389/fnins.2021.817218. eCollection 2021.
6
Endosomal trafficking defects alter neural progenitor proliferation and cause microcephaly.内体运输缺陷改变神经祖细胞的增殖并导致小头畸形。
Nat Commun. 2022 Jan 10;13(1):16. doi: 10.1038/s41467-021-27705-7.
7
Dissecting the molecular basis of human interneuron migration in forebrain assembloids from Timothy syndrome.剖析蒂莫西综合征患者前脑类器官中人类中间神经元迁移的分子基础。
Cell Stem Cell. 2022 Feb 3;29(2):248-264.e7. doi: 10.1016/j.stem.2021.11.011. Epub 2022 Jan 5.
8
Modeling human neurodevelopmental diseases with brain organoids.利用脑类器官模拟人类神经发育疾病。
Cell Regen. 2022 Jan 4;11(1):1. doi: 10.1186/s13619-021-00103-6.
9
Human Organoids for Predictive Toxicology Research and Drug Development.用于预测毒理学研究和药物开发的人类类器官
Front Genet. 2021 Nov 1;12:767621. doi: 10.3389/fgene.2021.767621. eCollection 2021.
10
Lissencephaly: Update on diagnostics and clinical management.无脑回畸形:诊断与临床管理的最新进展。
Eur J Paediatr Neurol. 2021 Nov;35:147-152. doi: 10.1016/j.ejpn.2021.09.013. Epub 2021 Oct 7.