• 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

自闭症谱系障碍的实验模型:iPS 细胞、啮齿动物和斑马鱼。

Experimental Models to Study Autism Spectrum Disorders: hiPSCs, Rodents and Zebrafish.

机构信息

Department of Zoology, Genetics and Physical Anthropology, Universidade de Santiago de Compostela, Campus de Lugo, 27002 Lugo, Spain.

Genomic Medicine Group, Center for Research in Molecular Medicine and Chronic Diseases (CiMUS), Universidade de Santiago de Compostela, 15706 Santiago de Compostela, Spain.

出版信息

Genes (Basel). 2020 Nov 20;11(11):1376. doi: 10.3390/genes11111376.

DOI:10.3390/genes11111376
PMID:33233737
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7699923/
Abstract

Autism Spectrum Disorders (ASD) affect around 1.5% of the global population, which manifest alterations in communication and socialization, as well as repetitive behaviors or restricted interests. ASD is a complex disorder with known environmental and genetic contributors; however, ASD etiology is far from being clear. In the past decades, many efforts have been put into developing new models to study ASD, both in vitro and in vivo. These models have a lot of potential to help to validate some of the previously associated risk factors to the development of the disorder, and to test new potential therapies that help to alleviate ASD symptoms. The present review is focused on the recent advances towards the generation of models for the study of ASD, which would be a useful tool to decipher the bases of the disorder, as well as to conduct drug screenings that hopefully lead to the identification of useful compounds to help patients deal with the symptoms of ASD.

摘要

自闭症谱系障碍(ASD)影响着全球约 1.5%的人口,其表现为沟通和社交能力的改变,以及重复行为或兴趣受限。ASD 是一种复杂的疾病,已知有环境和遗传因素的影响;然而,ASD 的病因还远未清楚。在过去的几十年中,人们做出了许多努力来开发新的模型,以研究 ASD,包括在体外和体内。这些模型具有很大的潜力,可以帮助验证一些先前与该疾病发展相关的风险因素,并测试新的潜在疗法,以帮助减轻 ASD 的症状。本综述集中讨论了 ASD 研究模型的最新进展,这将是一个有用的工具,可以深入了解该疾病的基础,并进行药物筛选,希望能找到有助于患者应对 ASD 症状的有用化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1efa/7699923/610208976824/genes-11-01376-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1efa/7699923/36c8f48861ab/genes-11-01376-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1efa/7699923/44c8802b9d6d/genes-11-01376-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1efa/7699923/c0e1b23776b5/genes-11-01376-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1efa/7699923/610208976824/genes-11-01376-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1efa/7699923/36c8f48861ab/genes-11-01376-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1efa/7699923/44c8802b9d6d/genes-11-01376-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1efa/7699923/c0e1b23776b5/genes-11-01376-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1efa/7699923/610208976824/genes-11-01376-g004.jpg

相似文献

1
Experimental Models to Study Autism Spectrum Disorders: hiPSCs, Rodents and Zebrafish.自闭症谱系障碍的实验模型:iPS 细胞、啮齿动物和斑马鱼。
Genes (Basel). 2020 Nov 20;11(11):1376. doi: 10.3390/genes11111376.
2
The use of stem cells to study autism spectrum disorder.利用干细胞研究自闭症谱系障碍。
Yale J Biol Med. 2015 Mar 4;88(1):5-16. eCollection 2015 Mar.
3
Zebrafish models of autism spectrum disorder.自闭症谱系障碍的斑马鱼模型
Exp Neurol. 2018 Jan;299(Pt A):207-216. doi: 10.1016/j.expneurol.2017.02.004. Epub 2017 Feb 3.
4
Understanding the molecular basis of autism in a dish using hiPSCs-derived neurons from ASD patients.利用自闭症谱系障碍(ASD)患者来源的人诱导多能干细胞(hiPSC)分化的神经元在体外模型中理解自闭症的分子基础。
Mol Brain. 2015 Sep 30;8(1):57. doi: 10.1186/s13041-015-0146-6.
5
Modeling autism in non-human primates: Opportunities and challenges.在非人类灵长类动物中模拟自闭症:机遇与挑战。
Autism Res. 2018 May;11(5):686-694. doi: 10.1002/aur.1945. Epub 2018 Mar 23.
6
Dysregulation of Neurite Outgrowth and Cell Migration in Autism and Other Neurodevelopmental Disorders.自闭症及其他神经发育障碍中神经突生长和细胞迁移的失调
Adv Neurobiol. 2020;25:109-153. doi: 10.1007/978-3-030-45493-7_5.
7
Current knowledge, challenges, new perspectives of the study, and treatments of Autism Spectrum Disorder.自闭症谱系障碍的研究现状、挑战、新视角和治疗方法。
Reprod Toxicol. 2021 Dec;106:82-93. doi: 10.1016/j.reprotox.2021.10.010. Epub 2021 Oct 22.
8
Modeling Autism Spectrum Disorders with Induced Pluripotent Stem Cell-Derived Brain Organoids.诱导多能干细胞衍生脑类器官模型构建自闭症谱系障碍。
Biomolecules. 2023 Jan 30;13(2):260. doi: 10.3390/biom13020260.
9
Spatial and Temporal Gene Function Studies in Rodents: Towards Gene-Based Therapies for Autism Spectrum Disorder.啮齿动物的时空基因功能研究:走向自闭症谱系障碍的基于基因的治疗方法。
Genes (Basel). 2021 Dec 23;13(1):28. doi: 10.3390/genes13010028.
10
Can we model autism using zebrafish?我们能否使用斑马鱼来模拟自闭症?
Dev Growth Differ. 2023 Oct;65(8):453-458. doi: 10.1111/dgd.12888. Epub 2023 Sep 16.

引用本文的文献

1
Animal models of autism spectrum disorder: Insights into genetic, structural and environmental models.自闭症谱系障碍的动物模型:对遗传、结构和环境模型的见解。
Vet Med (Praha). 2025 Jul 25;70(7):227-241. doi: 10.17221/87/2024-VETMED. eCollection 2025 Jul.
2
Etiologies underlying sex bias in autism spectrum disorder: a narrative review of preclinical rodent models.自闭症谱系障碍中性别偏见的潜在病因:对临床前啮齿动物模型的叙述性综述。
Ewha Med J. 2024 Apr;47(2):e18. doi: 10.12771/emj.2024.e18. Epub 2024 Apr 30.
3
Zebrafish as a tool for autism research: unraveling the roles of Shank3, Cntnap2, Neuroligin3, and Arid1b in synaptic and behavioral abnormalities.

本文引用的文献

1
Zebrafish as a tool to study schizophrenia-associated copy number variants.斑马鱼作为研究与精神分裂症相关的拷贝数变异的工具。
Dis Model Mech. 2020 Apr 29;13(4):dmm043877. doi: 10.1242/dmm.043877.
2
Modeling neuronal consequences of autism-associated gene regulatory variants with human induced pluripotent stem cells.利用人类诱导多能干细胞对自闭症相关基因调控变异的神经元后果进行建模。
Mol Autism. 2020 May 12;11(1):33. doi: 10.1186/s13229-020-00333-6.
3
Impaired expression of the COSMOC/MOCOS gene unit in ASD patient stem cells.自闭症谱系障碍患者干细胞中 COSMOC/MOCOS 基因单元表达受损。
斑马鱼作为自闭症研究的工具:揭示Shank3、Cntnap2、Neuroligin3和Arid1b在突触及行为异常中的作用
Neurogenetics. 2025 Jun 6;26(1):48. doi: 10.1007/s10048-025-00828-5.
4
Decoding the genetic landscape of autism: A comprehensive review.解码自闭症的基因图谱:全面综述。
World J Clin Pediatr. 2024 Sep 9;13(3):98468. doi: 10.5409/wjcp.v13.i3.98468.
5
Misdiagnosis in an Autistic Adolescent.一名自闭症青少年的误诊
Cureus. 2024 Aug 29;16(8):e68129. doi: 10.7759/cureus.68129. eCollection 2024 Aug.
6
The genetic landscape of autism spectrum disorder in the Middle Eastern population.中东人群自闭症谱系障碍的遗传图谱。
Front Genet. 2024 Mar 20;15:1363849. doi: 10.3389/fgene.2024.1363849. eCollection 2024.
7
Gastrointestinal dysfunction in the valproic acid induced model of social deficit in rats.大鼠丙戊酸诱导社会缺陷模型中的胃肠道功能障碍。
Auton Neurosci. 2024 Jun;253:103161. doi: 10.1016/j.autneu.2024.103161. Epub 2024 Feb 29.
8
Using Human-Induced Pluripotent Stem Cell Derived Neurons on Microelectrode Arrays to Model Neurological Disease: A Review.利用微电极阵列上的人诱导多能干细胞衍生神经元对神经疾病进行建模:综述。
Adv Sci (Weinh). 2023 Nov;10(33):e2301828. doi: 10.1002/advs.202301828. Epub 2023 Oct 20.
9
Circadian clock crosstalks with autism.生物钟与自闭症的相互作用。
Brain Behav. 2023 Dec;13(12):e3273. doi: 10.1002/brb3.3273. Epub 2023 Oct 8.
10
Unraveling the Role of Neuroligin3 in Autism Spectrum Disorders: Pathophysiological Insights and Targeted Therapies.解析神经黏连蛋白 3 在自闭症谱系障碍中的作用:病理生理学见解与靶向治疗。
CNS Neurol Disord Drug Targets. 2024;23(7):801-811. doi: 10.2174/1871527323666230727102244.
Mol Psychiatry. 2021 May;26(5):1606-1618. doi: 10.1038/s41380-020-0728-2. Epub 2020 Apr 23.
4
Zebrafish as a model for studying ovarian development: Recent advances from targeted gene knockout studies.斑马鱼作为研究卵巢发育的模型:来自靶向基因敲除研究的最新进展。
Mol Cell Endocrinol. 2020 May 1;507:110778. doi: 10.1016/j.mce.2020.110778. Epub 2020 Mar 3.
5
Gene replacement ameliorates deficits in mouse and human models of cyclin-dependent kinase-like 5 disorder.基因替换可改善周期蛋白依赖性激酶样 5 障碍的小鼠和人类模型中的缺陷。
Brain. 2020 Mar 1;143(3):811-832. doi: 10.1093/brain/awaa028.
6
Hyperactivity, Memory Defects, and Craniofacial Abnormalities in Zebrafish fmr1 Mutant Larvae.斑马鱼 fmr1 突变体幼虫的多动、记忆缺陷和颅面异常。
Behav Genet. 2020 May;50(3):152-160. doi: 10.1007/s10519-020-09995-7. Epub 2020 Feb 12.
7
De Novo ARID1B mutations cause growth delay associated with aberrant Wnt/β-catenin signaling.新生 ARID1B 突变导致生长迟缓,伴有异常的 Wnt/β-连环蛋白信号通路。
Hum Mutat. 2020 May;41(5):1012-1024. doi: 10.1002/humu.23990. Epub 2020 Mar 3.
8
Joining forces: the need to combine science and ethics to address problems of validity and translation in neuropsychiatry research using animal models.联合力量:使用动物模型进行神经精神医学研究时,需要将科学和伦理学结合起来解决有效性和转化问题。
Philos Ethics Humanit Med. 2020 Jan 23;15(1):1. doi: 10.1186/s13010-019-0085-4.
9
Oxytocin receptor signalling modulates novelty recognition but not social preference in zebrafish.催产素受体信号调节斑马鱼的新奇识别但不影响社交偏好。
J Neuroendocrinol. 2020 Apr;32(4):e12834. doi: 10.1111/jne.12834. Epub 2020 Feb 23.
10
Generation of a Novel Rat Model of Angelman Syndrome with a Complete Ube3a Gene Deletion.生成具有完整 Ube3a 基因缺失的新型 Angelman 综合征大鼠模型。
Autism Res. 2020 Mar;13(3):397-409. doi: 10.1002/aur.2267. Epub 2020 Jan 21.