Hippocampal and neocortical BRAF mutant non-expansive lesions in focal epilepsies.

IF 4 2区 医学 Q1 CLINICAL NEUROLOGY
Julie Lerond, Bertrand Mathon, Mélina Scopin, Lucia Nichelli, Justine Guégan, Céline Bertholle, Brigitte Izac, Muriel Andrieu, Thomas Gareau, Florian Donneger, Badreddine Mohand Oumoussa, Franck Letourneur, Suzanne Tran, Mathilde Bertrand, Isabelle Le Roux, Mehdi Touat, Sophie Dupont, Jean Christophe Poncer, Vincent Navarro, Franck Bielle
{"title":"Hippocampal and neocortical BRAF mutant non-expansive lesions in focal epilepsies.","authors":"Julie Lerond,&nbsp;Bertrand Mathon,&nbsp;Mélina Scopin,&nbsp;Lucia Nichelli,&nbsp;Justine Guégan,&nbsp;Céline Bertholle,&nbsp;Brigitte Izac,&nbsp;Muriel Andrieu,&nbsp;Thomas Gareau,&nbsp;Florian Donneger,&nbsp;Badreddine Mohand Oumoussa,&nbsp;Franck Letourneur,&nbsp;Suzanne Tran,&nbsp;Mathilde Bertrand,&nbsp;Isabelle Le Roux,&nbsp;Mehdi Touat,&nbsp;Sophie Dupont,&nbsp;Jean Christophe Poncer,&nbsp;Vincent Navarro,&nbsp;Franck Bielle","doi":"10.1111/nan.12937","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Mesial Temporal Lobe Epilepsy-associated Hippocampal Sclerosis (MTLE-HS) is a syndrome associated with various aetiologies. We previously identified CD34-positive extravascular stellate cells (CD34+ cells) possibly related to BRAF<sup>V600E</sup> oncogenic variant in a subset of MTLE-HS. We aimed to identify the BRAF<sup>V600E</sup> oncogenic variants and characterise the CD34+ cells.</p><p><strong>Methods: </strong>We analysed BRAF<sup>V600E</sup> oncogenic variant by digital droplet Polymerase Chain Reaction in 53 MTLE-HS samples (25 with CD34+ cells) and nine non-expansive neocortical lesions resected during epilepsy surgery (five with CD34+ cells). Ex vivo multi-electrode array recording, immunolabelling, methylation microarray and single nuclei RNAseq were performed on BRAF<sup>wildtype</sup> MTLE-HS and BRAF<sup>V600E</sup> mutant non-expansive lesion of hippocampus and/or neocortex.</p><p><strong>Results: </strong>We identified a BRAF<sup>V600E</sup> oncogenic variant in five MTLE-HS samples with CD34+ cells (19%) and in five neocortical samples with CD34+ cells (100%). Single nuclei RNAseq of resected samples revealed two unique clusters of abnormal cells (including CD34+ cells) associated with senescence and oligodendrocyte development in both hippocampal and neocortical BRAF<sup>V600E</sup> mutant samples. The co-expression of the oncogene-induced senescence marker p16<sup>INK4A</sup> and the outer subventricular zone radial glia progenitor marker HOPX in CD34+ cells was confirmed by multiplex immunostaining. Pseudotime analysis showed that abnormal cells share a common lineage from progenitors to myelinating oligodendrocytes. Epilepsy surgery led to seizure freedom in eight of the 10 patients with BRAF mutant lesions.</p><p><strong>Interpretation: </strong>BRAF<sup>V600E</sup> underlies a subset of MTLE-HS and epileptogenic non-expansive neocortical focal lesions. Detection of the oncogenic variant may help diagnosis and open perspectives for targeted therapies.</p>","PeriodicalId":19151,"journal":{"name":"Neuropathology and Applied Neurobiology","volume":" ","pages":"e12937"},"PeriodicalIF":4.0000,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neuropathology and Applied Neurobiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/nan.12937","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: Mesial Temporal Lobe Epilepsy-associated Hippocampal Sclerosis (MTLE-HS) is a syndrome associated with various aetiologies. We previously identified CD34-positive extravascular stellate cells (CD34+ cells) possibly related to BRAFV600E oncogenic variant in a subset of MTLE-HS. We aimed to identify the BRAFV600E oncogenic variants and characterise the CD34+ cells.

Methods: We analysed BRAFV600E oncogenic variant by digital droplet Polymerase Chain Reaction in 53 MTLE-HS samples (25 with CD34+ cells) and nine non-expansive neocortical lesions resected during epilepsy surgery (five with CD34+ cells). Ex vivo multi-electrode array recording, immunolabelling, methylation microarray and single nuclei RNAseq were performed on BRAFwildtype MTLE-HS and BRAFV600E mutant non-expansive lesion of hippocampus and/or neocortex.

Results: We identified a BRAFV600E oncogenic variant in five MTLE-HS samples with CD34+ cells (19%) and in five neocortical samples with CD34+ cells (100%). Single nuclei RNAseq of resected samples revealed two unique clusters of abnormal cells (including CD34+ cells) associated with senescence and oligodendrocyte development in both hippocampal and neocortical BRAFV600E mutant samples. The co-expression of the oncogene-induced senescence marker p16INK4A and the outer subventricular zone radial glia progenitor marker HOPX in CD34+ cells was confirmed by multiplex immunostaining. Pseudotime analysis showed that abnormal cells share a common lineage from progenitors to myelinating oligodendrocytes. Epilepsy surgery led to seizure freedom in eight of the 10 patients with BRAF mutant lesions.

Interpretation: BRAFV600E underlies a subset of MTLE-HS and epileptogenic non-expansive neocortical focal lesions. Detection of the oncogenic variant may help diagnosis and open perspectives for targeted therapies.

Abstract Image

局灶性癫痫患者的海马和新皮质BRAF突变非扩张性病变。
目的:颞叶癫痫相关海马硬化症(MTLE-HS)是一种病因多样的综合征。我们先前在MTLE-HS亚群中鉴定了CD34阳性的血管外星状细胞(CD34+细胞),可能与BRAFV600E致癌变体有关。我们的目的是鉴定BRAFV600E致癌变体并表征CD34+细胞。方法:我们通过数字液滴聚合酶链反应分析了53个MTLE-HS样本(25个带有CD34+细胞)和9个癫痫手术切除的非扩张性新皮质病变(5个带有CD34++细胞)中BRAFV600E的致癌变体。对BRAF野生型MTLE-HS和BRAFV600E突变型海马和/或新皮层非扩张性病变进行离体多电极阵列记录、免疫标记、甲基化微阵列和单核RNAseq。结果:我们在5个含有CD34+细胞的MTLE-HS样本(19%)和5个含有CD44+细胞的新皮质样本(100%)中鉴定出BRAFV600E致癌变体。切除样本的单核RNAseq显示,在海马和新皮质BRAFV600E突变样本中,有两组独特的异常细胞(包括CD34+细胞)与衰老和少突胶质细胞发育有关。通过多重免疫染色证实了癌基因诱导的衰老标记物p16INK4A和室下区外径向神经胶质祖细胞标记物HOPX在CD34+细胞中的共表达。假时间分析表明,异常细胞有一个共同的谱系,从祖细胞到有髓鞘的少突胶质细胞。癫痫手术导致10名BRAF突变病变患者中有8名患者无癫痫发作。解释:BRAFV600E是MTLE-HS亚群和致痫性非扩张性新皮质局灶性病变的基础。检测致癌变异可能有助于诊断,并为靶向治疗开辟前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
8.20
自引率
2.00%
发文量
87
审稿时长
6-12 weeks
期刊介绍: Neuropathology and Applied Neurobiology is an international journal for the publication of original papers, both clinical and experimental, on problems and pathological processes in neuropathology and muscle disease. Established in 1974, this reputable and well respected journal is an international journal sponsored by the British Neuropathological Society, one of the world leading societies for Neuropathology, pioneering research and scientific endeavour with a global membership base. Additionally members of the British Neuropathological Society get 50% off the cost of print colour on acceptance of their article.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信