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Reduced expression of BTBD10, an Akt activator, leads to motor neuron death
- Source :
- Cell Death & Differentiation. 19:1398-1407
- Publication Year :
- 2012
- Publisher :
- Springer Science and Business Media LLC, 2012.
-
Abstract
- BTBD10, an Akt interactor, activates Akt by decreasing the protein phosphatase 2A-mediated dephosphorylation and inactivation of Akt. Overexpression of BTBD10 suppresses motor neuron death that is induced by a familial amyotrophic lateral sclerosis (ALS)-linked superoxide dismutase 1 (SOD1) mutant, G93A-SOD1 in vitro. In this study, we further investigated the BTBD10-mediated suppression of motor neuron death. We found that the small interfering RNA-mediated inhibition of BTBD10 expression led to the death of cultured motor neurons. In Caenorhabditis elegans (C. elegans), disruption of the btbd-10 gene caused not only loss of neurons, including both motor and touch-receptor neurons, but also a locomotion defect. In addition, we found that the expression of BTBD10 was generally decreased in the motor neurons from patients of sporadic ALS and transgenic mice overexpressing G93A-SOD1 (G93A-SOD1-transgenic mice). Collectively, these results suggest that the reduced expression of BTBD10 leads to motor neuron death both in vitro and in vivo.
- Subjects :
- Genetically modified mouse
animal diseases
Phosphatase
SOD1
Mice, Transgenic
Biology
Mice
medicine
Animals
Humans
Gene Silencing
Amyotrophic lateral sclerosis
Caenorhabditis elegans
Molecular Biology
Protein kinase B
Motor Neurons
Genetics
Original Paper
Cell Death
Activator (genetics)
Intracellular Signaling Peptides and Proteins
Nuclear Proteins
nutritional and metabolic diseases
Cell Biology
Motor neuron
biology.organism_classification
medicine.disease
nervous system diseases
Cell biology
HEK293 Cells
medicine.anatomical_structure
nervous system
Proto-Oncogene Proteins c-akt
HeLa Cells
Subjects
Details
- ISSN :
- 14765403 and 13509047
- Volume :
- 19
- Database :
- OpenAIRE
- Journal :
- Cell Death & Differentiation
- Accession number :
- edsair.doi.dedup.....2c115d4970d136dc47be02b14c724de1
- Full Text :
- https://doi.org/10.1038/cdd.2012.19