• 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

在弗里德赖希共济失调的YG8R小鼠模型中存在两种不同的致病机制,即轴突逆行性神经病和胰腺衰老。

Two different pathogenic mechanisms, dying-back axonal neuropathy and pancreatic senescence, are present in the YG8R mouse model of Friedreich's ataxia.

作者信息

Mollá Belén, Riveiro Fátima, Bolinches-Amorós Arantxa, Muñoz-Lasso Diana C, Palau Francesc, González-Cabo Pilar

机构信息

Program in Rare and Genetic Diseases and IBV/CSIC Associated Unit at CIPF, Centro de Investigación Príncipe Felipe (CIPF), Valencia 46012, Spain CIBER de Enfermedades Raras (CIBERER), Valencia 28029, Spain.

Program in Rare and Genetic Diseases and IBV/CSIC Associated Unit at CIPF, Centro de Investigación Príncipe Felipe (CIPF), Valencia 46012, Spain Cell Therapy Program, Centro de Investigación Príncipe Felipe (CIPF), Valencia 46012, Spain.

出版信息

Dis Model Mech. 2016 Jun 1;9(6):647-57. doi: 10.1242/dmm.024273. Epub 2016 Apr 14.

DOI:10.1242/dmm.024273
PMID:27079523
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4920149/
Abstract

Frataxin (FXN) deficiency causes Friedreich's ataxia (FRDA), a multisystem disorder with neurological and non-neurological symptoms. FRDA pathophysiology combines developmental and degenerative processes of dorsal root ganglia (DRG), sensory nerves, dorsal columns and other central nervous structures. A dying-back mechanism has been proposed to explain the peripheral neuropathy and neuropathology. In addition, affected individuals have non-neuronal symptoms such as diabetes mellitus or glucose intolerance. To go further in the understanding of the pathogenic mechanisms of neuropathy and diabetes associated with the disease, we have investigated the humanized mouse YG8R model of FRDA. By biochemical and histopathological studies, we observed abnormal changes involving muscle spindles, dorsal root axons and DRG neurons, but normal findings in the posterior columns and brain, which agree with the existence of a dying-back process similar to that described in individuals with FRDA. In YG8R mice, we observed a large number of degenerated axons surrounded by a sheath exhibiting enlarged adaxonal compartments or by a thin disrupted myelin sheath. Thus, both axonal damage and defects in Schwann cells might underlie the nerve pathology. In the pancreas, we found a high proportion of senescent islets of Langerhans in YG8R mice, which decreases the β-cell number and islet mass to pathological levels, being unable to maintain normoglycemia. As a whole, these results confirm that the lack of FXN induces different pathogenic mechanisms in the nervous system and pancreas in the mouse model of FRDA: dying back of the sensory nerves, and pancreatic senescence.

摘要

弗里德赖希共济失调(FRDA)由铁调素(FXN)缺乏引起,是一种具有神经和非神经症状的多系统疾病。FRDA的病理生理学结合了背根神经节(DRG)、感觉神经、后索和其他中枢神经结构的发育和退化过程。有人提出一种逆行性变性机制来解释周围神经病变和神经病理学。此外,受影响个体还有非神经元症状,如糖尿病或葡萄糖不耐受。为了进一步了解与该疾病相关的神经病变和糖尿病的致病机制,我们研究了FRDA的人源化小鼠YG8R模型。通过生化和组织病理学研究,我们观察到涉及肌梭、背根轴突和DRG神经元的异常变化,但后索和大脑未见异常,这与FRDA患者中描述的逆行性变性过程一致。在YG8R小鼠中,我们观察到大量退化的轴突被具有扩大的轴突旁间隙的鞘或薄的、破坏的髓鞘包围。因此,轴突损伤和施万细胞缺陷可能是神经病理学的基础。在胰腺中,我们发现YG8R小鼠中有高比例的衰老胰岛,这将β细胞数量和胰岛质量降低到病理水平,无法维持正常血糖水平。总体而言,这些结果证实,在FRDA小鼠模型中,FXN的缺乏在神经系统和胰腺中诱导了不同的致病机制:感觉神经的逆行性变性和胰腺衰老。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09a0/4920149/02790ad64003/dmm-9-024273-g8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09a0/4920149/9d75af1bda84/dmm-9-024273-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09a0/4920149/83837b68c0bf/dmm-9-024273-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09a0/4920149/a1c68be0170d/dmm-9-024273-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09a0/4920149/b743e5c61376/dmm-9-024273-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09a0/4920149/37d439c8430a/dmm-9-024273-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09a0/4920149/4c4e10ceb88f/dmm-9-024273-g6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09a0/4920149/5469e4a2f8c8/dmm-9-024273-g7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09a0/4920149/02790ad64003/dmm-9-024273-g8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09a0/4920149/9d75af1bda84/dmm-9-024273-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09a0/4920149/83837b68c0bf/dmm-9-024273-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09a0/4920149/a1c68be0170d/dmm-9-024273-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09a0/4920149/b743e5c61376/dmm-9-024273-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09a0/4920149/37d439c8430a/dmm-9-024273-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09a0/4920149/4c4e10ceb88f/dmm-9-024273-g6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09a0/4920149/5469e4a2f8c8/dmm-9-024273-g7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09a0/4920149/02790ad64003/dmm-9-024273-g8.jpg

相似文献

1
Two different pathogenic mechanisms, dying-back axonal neuropathy and pancreatic senescence, are present in the YG8R mouse model of Friedreich's ataxia.在弗里德赖希共济失调的YG8R小鼠模型中存在两种不同的致病机制,即轴突逆行性神经病和胰腺衰老。
Dis Model Mech. 2016 Jun 1;9(6):647-57. doi: 10.1242/dmm.024273. Epub 2016 Apr 14.
2
Phosphodiesterase Inhibitors Revert Axonal Dystrophy in Friedreich's Ataxia Mouse Model.磷酸二酯酶抑制剂逆转弗里德里希共济失调小鼠模型中的轴突萎缩。
Neurotherapeutics. 2019 Apr;16(2):432-449. doi: 10.1007/s13311-018-00706-z.
3
Pathology and pathogenesis of sensory neuropathy in Friedreich's ataxia.弗里德里希共济失调症感觉神经病的病理和发病机制。
Acta Neuropathol. 2010 Jul;120(1):97-108. doi: 10.1007/s00401-010-0675-0. Epub 2010 Mar 26.
4
A novel GAA-repeat-expansion-based mouse model of Friedreich's ataxia.一种基于GAA重复扩增的新型弗里德赖希共济失调小鼠模型。
Dis Model Mech. 2015 Mar;8(3):225-35. doi: 10.1242/dmm.018952. Epub 2015 Feb 13.
5
Mitochondrial pathophysiology in Friedreich's ataxia.弗里德里希共济失调症中的线粒体病理生理学。
J Neurochem. 2013 Aug;126 Suppl 1:53-64. doi: 10.1111/jnc.12303.
6
Mitochondrial damage and senescence phenotype of cells derived from a novel frataxin G127V point mutation mouse model of Friedreich's ataxia.弗里德里希共济失调症新型铁蛋白 G127V 点突变小鼠模型来源的细胞线粒体损伤和衰老表型。
Dis Model Mech. 2020 Jul 27;13(7):dmm045229. doi: 10.1242/dmm.045229.
7
Frataxin deficiency leads to defects in expression of antioxidants and Nrf2 expression in dorsal root ganglia of the Friedreich's ataxia YG8R mouse model.弗里德里希共济失调 YG8R 小鼠模型中 frataxin 缺乏导致抗氧化剂表达和 Nrf2 表达缺陷在背根神经节中。
Antioxid Redox Signal. 2013 Nov 1;19(13):1481-93. doi: 10.1089/ars.2012.4537. Epub 2013 Mar 28.
8
Transplantation of wild-type mouse hematopoietic stem and progenitor cells ameliorates deficits in a mouse model of Friedreich's ataxia.野生型小鼠造血干细胞和祖细胞移植可改善弗里德里希共济失调症小鼠模型的缺陷。
Sci Transl Med. 2017 Oct 25;9(413). doi: 10.1126/scitranslmed.aaj2347.
9
The dorsal root ganglion in Friedreich's ataxia.弗里德里希共济失调中的背根神经节。
Acta Neuropathol. 2009 Dec;118(6):763-76. doi: 10.1007/s00401-009-0589-x. Epub 2009 Aug 30.
10
Frataxin gene editing rescues Friedreich's ataxia pathology in dorsal root ganglia organoid-derived sensory neurons.弗里德赖希共济失调基因编辑可挽救背根神经节类器官衍生的感觉神经元中的弗里德赖希共济失调病理状态。
Nat Commun. 2020 Aug 21;11(1):4178. doi: 10.1038/s41467-020-17954-3.

引用本文的文献

1
A new FRDA mouse model [ :YG8s(GAA) > 800] with more than 800 GAA repeats.一种新的具有超过800个GAA重复序列的弗里德赖希共济失调(FRDA)小鼠模型[:YG8s(GAA) > 800] 。
Front Neurosci. 2023 Jan 26;17:930422. doi: 10.3389/fnins.2023.930422. eCollection 2023.
2
Ketolysis is Required for the Proper Development and Function of the Somatosensory Nervous System.躯体感觉神经系统的正常发育和功能需要酮体分解。
bioRxiv. 2023 Mar 30:2023.01.11.523492. doi: 10.1101/2023.01.11.523492.
3
Acute Cerebellar Inflammation and Related Ataxia: Mechanisms and Pathophysiology.

本文引用的文献

1
Unveiling a common mechanism of apoptosis in β-cells and neurons in Friedreich's ataxia.揭示弗里德赖希共济失调中β细胞和神经元凋亡的共同机制。
Hum Mol Genet. 2015 Apr 15;24(8):2274-86. doi: 10.1093/hmg/ddu745. Epub 2014 Dec 30.
2
Cellular, molecular and functional characterisation of YAC transgenic mouse models of Friedreich ataxia.弗里德赖希共济失调YAC转基因小鼠模型的细胞、分子及功能特性研究
PLoS One. 2014 Sep 8;9(9):e107416. doi: 10.1371/journal.pone.0107416. eCollection 2014.
3
Mitochondrial dysfunction induced by frataxin deficiency is associated with cellular senescence and abnormal calcium metabolism.
急性小脑炎症及相关共济失调:机制与病理生理学
Brain Sci. 2022 Mar 10;12(3):367. doi: 10.3390/brainsci12030367.
4
Molecular Defects in Friedreich's Ataxia: Convergence of Oxidative Stress and Cytoskeletal Abnormalities.弗里德赖希共济失调的分子缺陷:氧化应激与细胞骨架异常的共同作用
Front Mol Biosci. 2020 Nov 9;7:569293. doi: 10.3389/fmolb.2020.569293. eCollection 2020.
5
Phosphodiesterase Inhibitors Revert Axonal Dystrophy in Friedreich's Ataxia Mouse Model.磷酸二酯酶抑制剂逆转弗里德里希共济失调小鼠模型中的轴突萎缩。
Neurotherapeutics. 2019 Apr;16(2):432-449. doi: 10.1007/s13311-018-00706-z.
6
Reversible Axonal Dystrophy by Calcium Modulation in Frataxin-Deficient Sensory Neurons of YG8R Mice.YG8R小鼠中,在缺乏共济蛋白的感觉神经元中通过钙调节引起的可逆性轴突营养不良。
Front Mol Neurosci. 2017 Aug 30;10:264. doi: 10.3389/fnmol.2017.00264. eCollection 2017.
7
Circulating miR-323-3p is a biomarker for cardiomyopathy and an indicator of phenotypic variability in Friedreich's ataxia patients.循环 miR-323-3p 是心肌病的生物标志物,也是弗里德里希共济失调患者表型变异性的指标。
Sci Rep. 2017 Jul 12;7(1):5237. doi: 10.1038/s41598-017-04996-9.
铁蛋白缺乏诱导的线粒体功能障碍与细胞衰老和异常钙代谢有关。
Front Cell Neurosci. 2014 May 13;8:124. doi: 10.3389/fncel.2014.00124. eCollection 2014.
4
Mitochondrial pathophysiology in Friedreich's ataxia.弗里德里希共济失调症中的线粒体病理生理学。
J Neurochem. 2013 Aug;126 Suppl 1:53-64. doi: 10.1111/jnc.12303.
5
Friedreich ataxia: neuropathology revised.弗里德赖希共济失调:神经病理学修订版。
J Neuropathol Exp Neurol. 2013 Feb;72(2):78-90. doi: 10.1097/NEN.0b013e31827e5762.
6
Central role and mechanisms of β-cell dysfunction and death in friedreich ataxia-associated diabetes.弗里德里希共济失调相关糖尿病中β细胞功能障碍和死亡的中心作用和机制。
Ann Neurol. 2012 Dec;72(6):971-82. doi: 10.1002/ana.23698.
7
Can loss of muscle spindle afferents explain the ataxic gait in Riley-Day syndrome?肌梭传入纤维丧失能否解释赖利-戴综合征的共济失调步态?
Brain. 2011 Nov;134(Pt 11):3198-208. doi: 10.1093/brain/awr168.
8
Overexpression of human and fly frataxins in Drosophila provokes deleterious effects at biochemical, physiological and developmental levels.人源和果蝇 frataxin 的过表达在生化、生理和发育水平引起有害影响。
PLoS One. 2011;6(7):e21017. doi: 10.1371/journal.pone.0021017. Epub 2011 Jul 11.
9
Too many breaks (brakes): pancreatic β-cell senescence leads to diabetes.休息太多(刹车):胰腺β细胞衰老导致糖尿病。
Cell Cycle. 2011 Aug 1;10(15):2471-84. doi: 10.4161/cc.10.15.16741.
10
The cerebellar component of Friedreich's ataxia.弗里德里希共济失调的小脑成分。
Acta Neuropathol. 2011 Sep;122(3):323-30. doi: 10.1007/s00401-011-0844-9. Epub 2011 Jun 3.