Pten对DRG感觉神经元多样化的内在控制。

Alejandra Fernandez, Nick Sarn, Charis Eng, Kevin M Wright
{"title":"Pten对DRG感觉神经元多样化的内在控制。","authors":"Alejandra Fernandez, Nick Sarn, Charis Eng, Kevin M Wright","doi":"10.1101/2023.08.04.552039","DOIUrl":null,"url":null,"abstract":"<p><p>Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder characterized by deficits in social interactions, repetitive behaviors, and hyper- or hyposensitivity to sensory stimuli. The mechanisms underlying the emergence of sensory features in ASD are not fully understood, but recent studies in rodent models highlight that these may result from differences in primary sensory neurons themselves. We examined sensory behaviors in a <i>Pten</i> haploinsufficient mouse model ( <i>Pten <sup>Het</sup></i> ) for syndromic ASD and identified elevated responses to mechanical stimuli and a higher threshold to thermal responses. Transcriptomic and <i>in vivo</i> anatomical analysis identified alterations in subtype-specific markers of primary somatosensory neurons in <i>Pten <sup>Het</sup></i> dorsal root ganglia (DRG). These defects emerge early during DRG development and involve dysregulation of multiple signaling pathways downstream of <i>Pten</i> . Finally, we show that mice harboring an ASD-associated mutation ( <i>Pten <sup>Y69H</sup></i> ) also show altered expression of somatosensory neuron subtype-specific markers. Together, these results show that precise levels of <i>Pten</i> are required for proper somatosensory development and provide insight into the molecular and cellular basis of sensory abnormalities in a model for syndromic ASD.</p>","PeriodicalId":72407,"journal":{"name":"bioRxiv : the preprint server for biology","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10541114/pdf/","citationCount":"0","resultStr":"{\"title\":\"Altered primary somatosensory neuron development in a <i>Pten</i> heterozygous model for autism spectrum disorder.\",\"authors\":\"Alejandra Fernandez, Nick Sarn, Charis Eng, Kevin M Wright\",\"doi\":\"10.1101/2023.08.04.552039\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder characterized by deficits in social interactions, repetitive behaviors, and hyper- or hyposensitivity to sensory stimuli. The mechanisms underlying the emergence of sensory features in ASD are not fully understood, but recent studies in rodent models highlight that these may result from differences in primary sensory neurons themselves. We examined sensory behaviors in a <i>Pten</i> haploinsufficient mouse model ( <i>Pten <sup>Het</sup></i> ) for syndromic ASD and identified elevated responses to mechanical stimuli and a higher threshold to thermal responses. Transcriptomic and <i>in vivo</i> anatomical analysis identified alterations in subtype-specific markers of primary somatosensory neurons in <i>Pten <sup>Het</sup></i> dorsal root ganglia (DRG). These defects emerge early during DRG development and involve dysregulation of multiple signaling pathways downstream of <i>Pten</i> . Finally, we show that mice harboring an ASD-associated mutation ( <i>Pten <sup>Y69H</sup></i> ) also show altered expression of somatosensory neuron subtype-specific markers. Together, these results show that precise levels of <i>Pten</i> are required for proper somatosensory development and provide insight into the molecular and cellular basis of sensory abnormalities in a model for syndromic ASD.</p>\",\"PeriodicalId\":72407,\"journal\":{\"name\":\"bioRxiv : the preprint server for biology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-01-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10541114/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"bioRxiv : the preprint server for biology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1101/2023.08.04.552039\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"bioRxiv : the preprint server for biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2023.08.04.552039","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

磷酸酶和紧张素同源物(PTEN)调节发育中的外周神经系统(PNS)中神经营养因子受体下游的细胞内生存和分化信号通路。尽管在大脑发育的背景下进行了充分的研究,但我们对PTEN在PNS中的体内作用的理解仅限于神经性疼痛和神经损伤模型。在这里,我们评估了PTEN信号的改变如何影响外周体感回路的发育。我们发现,在Pten杂合子(Pten-Het)小鼠的背根神经节(DRG)内的感觉神经元表现出神经元亚型多样化的缺陷。Pten-Het小鼠的DRG分化异常发生在发育早期,神经元亚群同时表达祖细胞和神经元标志物。Pten-Het小鼠的DRG显示Pten下游mTOR和GSK-3β信号通路的失调。最后,我们发现患有自闭症相关Pten突变(Pten Y68H/+)的小鼠表现出DRG发育异常。因此,我们发现PTEN信号在DRG发育过程中初级感觉神经元群体的内在多样化中起着至关重要的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Altered primary somatosensory neuron development in a Pten heterozygous model for autism spectrum disorder.

Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder characterized by deficits in social interactions, repetitive behaviors, and hyper- or hyposensitivity to sensory stimuli. The mechanisms underlying the emergence of sensory features in ASD are not fully understood, but recent studies in rodent models highlight that these may result from differences in primary sensory neurons themselves. We examined sensory behaviors in a Pten haploinsufficient mouse model ( Pten Het ) for syndromic ASD and identified elevated responses to mechanical stimuli and a higher threshold to thermal responses. Transcriptomic and in vivo anatomical analysis identified alterations in subtype-specific markers of primary somatosensory neurons in Pten Het dorsal root ganglia (DRG). These defects emerge early during DRG development and involve dysregulation of multiple signaling pathways downstream of Pten . Finally, we show that mice harboring an ASD-associated mutation ( Pten Y69H ) also show altered expression of somatosensory neuron subtype-specific markers. Together, these results show that precise levels of Pten are required for proper somatosensory development and provide insight into the molecular and cellular basis of sensory abnormalities in a model for syndromic ASD.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Self-supervised segmentation and characterization of fiber bundles in anatomic tracing data. Single neuron contributions to the auditory brainstem EEG. Neural substrates of cold nociception in Drosophila larva. Inversions Can Accumulate Balanced Sexual Antagonism: Evidence from Simulations and Drosophila Experiments. Programming megakaryocytes to produce engineered platelets for delivering non-native proteins.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1