Literature DB >> 15378322

14-3-3 proteins in Lewy body-like hyaline inclusions in patients with sporadic amyotrophic lateral sclerosis.

Yasuhiro Kawamoto1, Ichiro Akiguchi, Shinichi Nakamura, Herbert Budka.   

Abstract

14-3-3 proteins are highly conserved eukaryotic proteins that regulate various types of signal transduction pathways through phosphorylation-dependent protein-protein interactions. 14-3-3 mRNAs have been shown to be up-regulated in the injured rat motor neurons and in the spinal cords of patients with amyotrophic lateral sclerosis (ALS). To investigate the role of 14-3-3 proteins in ALS, we performed immunohistochemical studies on 14-3-3 using autopsied spinal cords from patients with sporadic ALS (sALS) and non-ALS subjects without spinal cord involvement. In the anterior horn of both groups, strong 14-3-3 immunoreactivity was observed in the somata and proximal processes of motor neurons. Many spheroids from all of the sALS cases were also immunopositive for 14-3-3. In addition, Lewy body-like hyaline inclusions (LBHIs), which were present in some sALS cases, were intensely immunostained. Our findings suggest that even in the severely affected anterior horn of patients with sALS, remaining motor neurons may contain abundant 14-3-3 proteins, and that 14-3-3 proteins may be partly associated with the pathogenesis of sALS, in particular with the formation of LBHIs.

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Year:  2004        PMID: 15378322     DOI: 10.1007/s00401-004-0923-2

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  6 in total

1.  14-3-3 protein targets misfolded chaperone-associated proteins to aggresomes.

Authors:  Zhe Xu; Kourtney Graham; Molly Foote; Fengshan Liang; Raed Rizkallah; Myra Hurt; Yanchang Wang; Yuying Wu; Yi Zhou
Journal:  J Cell Sci       Date:  2013-07-10       Impact factor: 5.285

2.  Colocalization of 14-3-3 proteins with SOD1 in Lewy body-like hyaline inclusions in familial amyotrophic lateral sclerosis cases and the animal model.

Authors:  Yoko Okamoto; Yoshitomo Shirakashi; Masafumi Ihara; Makoto Urushitani; Miki Oono; Yasuhiro Kawamoto; Hirofumi Yamashita; Shun Shimohama; Shinsuke Kato; Asao Hirano; Hidekazu Tomimoto; Hidefumi Ito; Ryosuke Takahashi
Journal:  PLoS One       Date:  2011-05-31       Impact factor: 3.240

Review 3.  Phosphorylation of Threonine 175 Tau in the Induction of Tau Pathology in Amyotrophic Lateral Sclerosis-Frontotemporal Spectrum Disorder (ALS-FTSD). A Review.

Authors:  Alexander J Moszczynski; Matthew A Hintermayer; Michael J Strong
Journal:  Front Neurosci       Date:  2018-04-20       Impact factor: 4.677

4.  Characterization of detergent-insoluble proteins in ALS indicates a causal link between nitrative stress and aggregation in pathogenesis.

Authors:  Manuela Basso; Giuseppina Samengo; Giovanni Nardo; Tania Massignan; Giuseppina D'Alessandro; Silvia Tartari; Lavinia Cantoni; Marianna Marino; Cristina Cheroni; Silvia De Biasi; Maria Teresa Giordana; Michael J Strong; Alvaro G Estevez; Mario Salmona; Caterina Bendotti; Valentina Bonetto
Journal:  PLoS One       Date:  2009-12-02       Impact factor: 3.240

Review 5.  Neuroprotective function of 14-3-3 proteins in neurodegeneration.

Authors:  Tadayuki Shimada; Alyson E Fournier; Kanato Yamagata
Journal:  Biomed Res Int       Date:  2013-12-02       Impact factor: 3.411

6.  Genealogy of the neurodegenerative diseases based on a meta-analysis of age-stratified incidence data.

Authors:  Daniela Gerovska; Haritz Irizar; David Otaegi; Isidre Ferrer; Adolfo López de Munain; Marcos J Araúzo-Bravo
Journal:  Sci Rep       Date:  2020-11-03       Impact factor: 4.379

  6 in total

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