Flip and flop splice variants of AMPA receptor subunits in the spinal cord of amyotrophic lateral sclerosis

Synapse ◽  
2002 ◽  
Vol 45 (4) ◽  
pp. 245-249 ◽  
Author(s):  
Masahiko Tomiyama ◽  
Rafael Rodríguez-Puertas ◽  
Roser Cortés ◽  
Angel Pazos ◽  
José M. Palacios ◽  
...  
Keyword(s):  
Spinal Cord ◽  
Amyotrophic Lateral Sclerosis ◽  
Ampa Receptor ◽  
Splice Variants ◽  
Lateral Sclerosis

Selective upregulation of the flip-flop splice variants of AMPA receptor subunits in the rat spinal cord after hindpaw inflammation

2001 ◽  
Vol 88 (1-2) ◽  
pp. 186-193 ◽  
Author(s):  
Qi-Qi Zhou ◽  
Hiroki Imbe ◽  
Shiping Zou ◽  
Ronald Dubner ◽  
Ke Ren
Keyword(s):  
Spinal Cord ◽  
Ampa Receptor ◽  
Splice Variants ◽  
Rat Spinal Cord ◽  
Flip Flop

scholarly journals A 14-3-3 mRNA Is Up-Regulated in Amyotrophic Lateral Sclerosis Spinal Cord

2008 ◽  
Vol 75 (6) ◽  
pp. 2511-2520 ◽  
Author(s):  
Andrea Malaspina ◽  
Narendra Kaushik ◽  
Jackie de Belleroche
Keyword(s):  
Spinal Cord ◽  
Amyotrophic Lateral Sclerosis ◽  
Lateral Sclerosis

scholarly journals RBM45 Modulates the Antioxidant Response in Amyotrophic Lateral Sclerosis through Interactions with KEAP1

2015 ◽  
Vol 35 (14) ◽  
pp. 2385-2399 ◽  
Author(s):  
Nadine Bakkar ◽  
Arianna Kousari ◽  
Tina Kovalik ◽  
Yang Li ◽  
Robert Bowser
Keyword(s):  
Oxidative Stress ◽  
Spinal Cord ◽  
Amyotrophic Lateral Sclerosis ◽  
Motor Neurons ◽  
Rna Binding ◽  
Binding Protein ◽  
Rna Binding Protein ◽  
Antioxidant Response ◽  
Cytoplasmic Inclusions ◽  
Lateral Sclerosis

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by the selective loss of motor neurons. Various factors contribute to the disease, including RNA binding protein dysregulation and oxidative stress, but their exact role in pathogenic mechanisms remains unclear. We have recently linked another RNA binding protein, RBM45, to ALS via increased levels of protein in the cerebrospinal fluid of ALS patients and its localization to cytoplasmic inclusions in ALS motor neurons. Here we show RBM45 nuclear exit in ALS spinal cord motor neurons compared to controls, a phenotype recapitulatedin vitroin motor neurons treated with oxidative stressors. We find that RBM45 binds and stabilizes KEAP1, the inhibitor of the antioxidant response transcription factor NRF2. ALS lumbar spinal cord lysates similarly show increased cytoplasmic binding of KEAP1 and RBM45. Binding of RBM45 to KEAP1 impedes the protective antioxidant response, thus contributing to oxidative stress-induced cellular toxicity. Our findings thus describe a novel link between a mislocalized RNA binding protein implicated in ALS (RBM45) and dysregulation of the neuroprotective antioxidant response seen in the disease.

scholarly journals Optineurin pathology in the spinal cord of amyotrophic lateral sclerosis/parkinsonism-dementia complex patients in Kii Peninsula, Japan

2018 ◽  
Vol 28 (3) ◽  
pp. 422-426 ◽  
Author(s):  
Satoru Morimoto ◽  
Hiroyuki Hatsuta ◽  
Rie Motoyama ◽  
Yasumasa Kokubo ◽  
Hiroyuki Ishiura ◽  
...  
Keyword(s):  
Spinal Cord ◽  
Amyotrophic Lateral Sclerosis ◽  
Kii Peninsula ◽  
Complex Patients ◽  
Lateral Sclerosis

A longitudinal DTI and histological study of the spinal cord reveals early pathological alterations in G93A-SOD1 mouse model of amyotrophic lateral sclerosis

2017 ◽  
Vol 293 ◽  
pp. 43-52 ◽  
Author(s):  
Stefania Marcuzzo ◽  
Silvia Bonanno ◽  
Matteo Figini ◽  
Alessandro Scotti ◽  
Ileana Zucca ◽  
...  
Keyword(s):  
Spinal Cord ◽  
Amyotrophic Lateral Sclerosis ◽  
Mouse Model ◽  
Histological Study ◽  
G93a Sod1 Mouse ◽  
Sod1 Mouse ◽  
G93a Sod1 ◽  
Lateral Sclerosis

scholarly journals Spinal cord homogenates from SOD1 familial amyotrophic lateral sclerosis induce SOD1 aggregation in living cells

PLoS ONE ◽  
2017 ◽  
Vol 12 (9) ◽  
pp. e0184384 ◽  
Author(s):  
Edward Pokrishevsky ◽  
Ran Ha Hong ◽  
Ian R. Mackenzie ◽  
Neil R. Cashman
Keyword(s):  
Spinal Cord ◽  
Amyotrophic Lateral Sclerosis ◽  
Living Cells ◽  
Familial Amyotrophic Lateral Sclerosis ◽  
Lateral Sclerosis

Ultrastructural features of aberrant glial cells isolated from the spinal cord of paralytic rats expressing the amyotrophic lateral sclerosis-linked SOD1G93A mutation

2017 ◽  
Vol 370 (3) ◽  
pp. 391-401 ◽  
Author(s):  
Marcie Jiménez-Riani ◽  
Pablo Díaz-Amarilla ◽  
Eugenia Isasi ◽  
Gabriela Casanova ◽  
Luis Barbeito ◽  
...  
Keyword(s):  
Spinal Cord ◽  
Amyotrophic Lateral Sclerosis ◽  
Glial Cells ◽  
Aberrant Glial Cells ◽  
Lateral Sclerosis
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