Literature DB >> 18097163

Motor neuron disease and frontotemporal lobar degeneration: a tale of two disorders linked to TDP-43.

Lauren B Elman1, Leo McCluskey, Murray Grossman.   

Abstract

Motor neuron disease (MND) is a neurodegenerative condition long thought to be associated only with motor weakness. Recent work now shows that cognitive difficulties are present in up to half of the patients with this disorder. About 5-10% of patients with MND have a frank dementia that resembles frontotemporal lobar degeneration (FTLD). Imaging studies show quantitative abnormalities that resemble FTLD. Moreover, biochemical studies of ubiquinated histopathologic abnormalities in MND and FTLD reveal identical inclusions of TDP-43. These findings underline a fundamental link between MND and FTLD. This paper reviews this body of work.

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Year:  2007        PMID: 18097163     DOI: 10.1159/000109762

Source DB:  PubMed          Journal:  Neurosignals        ISSN: 1424-862X


  8 in total

Review 1.  Amyotrophic lateral sclerosis, frontotemporal dementia and beyond: the TDP-43 diseases.

Authors:  Felix Geser; Maria Martinez-Lage; Linda K Kwong; Virginia M-Y Lee; John Q Trojanowski
Journal:  J Neurol       Date:  2009-03-07       Impact factor: 4.849

2.  TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis.

Authors:  Vivianna M Van Deerlin; James B Leverenz; Lynn M Bekris; Thomas D Bird; Wuxing Yuan; Lauren B Elman; Dana Clay; Elisabeth McCarty Wood; Alice S Chen-Plotkin; Maria Martinez-Lage; Ellen Steinbart; Leo McCluskey; Murray Grossman; Manuela Neumann; I-Lin Wu; Wei-Shiung Yang; Robert Kalb; Douglas R Galasko; Thomas J Montine; John Q Trojanowski; Virginia M-Y Lee; Gerard D Schellenberg; Chang-En Yu
Journal:  Lancet Neurol       Date:  2008-04-07       Impact factor: 44.182

Review 3.  Amyotrophic lateral sclerosis and frontotemporal lobar degeneration: a spectrum of TDP-43 proteinopathies.

Authors:  Felix Geser; Virginia M-Y Lee; John Q Trojanowski
Journal:  Neuropathology       Date:  2010-01-25       Impact factor: 1.906

4.  Elevated expression of TDP-43 in the forebrain of mice is sufficient to cause neurological and pathological phenotypes mimicking FTLD-U.

Authors:  Kuen-Jer Tsai; Chun-Hung Yang; Yen-Hsin Fang; Kuan-Hung Cho; Wei-Lin Chien; Wei-Ting Wang; Tzu-Wei Wu; Ching-Po Lin; Wen-Mei Fu; Che-Kun James Shen
Journal:  J Exp Med       Date:  2010-07-26       Impact factor: 14.307

5.  Exposure to ALS-FTD-CSF generates TDP-43 aggregates in glioblastoma cells through exosomes and TNTs-like structure.

Authors:  Xuebing Ding; Mingming Ma; Junfang Teng; Robert K F Teng; Shuang Zhou; Jingzheng Yin; Ekokobe Fonkem; Jason H Huang; Erxi Wu; Xuejing Wang
Journal:  Oncotarget       Date:  2015-09-15

6.  TDP-43 Vasculopathy in the Spinal Cord in Sporadic Amyotrophic Lateral Sclerosis (sALS) and Frontal Cortex in sALS/FTLD-TDP.

Authors:  Isidro Ferrer; Pol Andrés-Benito; Margarita Carmona; Abdelilah Assialioui; Mónica Povedano
Journal:  J Neuropathol Exp Neurol       Date:  2021-02-22       Impact factor: 3.685

Review 7.  Exploring Neurofilament Light Chain and Exosomes in the Genetic Forms of Frontotemporal Dementia.

Authors:  Roberta Zanardini; Claudia Saraceno; Luisa Benussi; Rosanna Squitti; Roberta Ghidoni
Journal:  Front Neurosci       Date:  2022-01-25       Impact factor: 4.677

8.  Functional mapping of the interaction between TDP-43 and hnRNP A2 in vivo.

Authors:  Andrea D'Ambrogio; Emanuele Buratti; Cristiana Stuani; Corrado Guarnaccia; Maurizio Romano; Youhna M Ayala; Francisco E Baralle
Journal:  Nucleic Acids Res       Date:  2009-05-08       Impact factor: 16.971

  8 in total

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