TY - JOUR
T1 - Proteomic profiling of the spinal cord in ALS
T2 - decreased ATP5D levels suggest synaptic dysfunction in ALS pathogenesis
AU - Engelen-Lee, Jooyeon
AU - Blokhuis, Anna M.
AU - Spliet, Wim G.M.
AU - Pasterkamp, R. Jeroen
AU - Aronica, Eleonora
AU - Demmers, Jeroen A A
AU - Broekhuizen, Roel
AU - Nardo, Giovanni
AU - Bovenschen, Niels
AU - Van Den Berg, Leonard H.
N1 - Publisher Copyright:
© 2016 World Federation of Neurology on behalf of the Research Group on Motor Neuron Diseases.
PY - 2017/4/3
Y1 - 2017/4/3
N2 - Background: We aimed to gain new insights into the pathogenesis of sporadic ALS (sALS) through a comprehensive proteomic analysis. Methods: Protein profiles of the anterior and posterior horn in post-mortem spinal cord samples of 10 ALS patients and 10 controls were analysed using 2D-differential gel electrophoresis. The identified protein spots with statistically significant level changes and a spot ratio >2.0 were analysed by LC-MS/MS. Results: In the posterior horn only 3 proteins were differentially expressed. In the anterior horn, 16 proteins with increased levels and 2 proteins with decreased levels were identified in ALS compared to controls. The identified proteins were involved in mitochondrial metabolism, calcium homeostasis, protein metabolism, glutathione homeostasis, protein transport and snRNP assembly. The two proteins with decreased levels, ATP5D and calmodulin, were validated by Western blot and immunostaining. Immunohistochemical and immunofluorescent double staining of ATP5D and synaptophysin showed that the reduction of ATP5D was most pronounced at synapses. Conclusions: We speculate that mitochondrial dysfunction in synaptic clefts could play an important role in sALS pathogenesis. A similar approach revealed decreased calmodulin expression mainly in the neuronal body and dendrites of ALS patients. These findings contribute to a deeper understanding of the disease process underlying ALS.
AB - Background: We aimed to gain new insights into the pathogenesis of sporadic ALS (sALS) through a comprehensive proteomic analysis. Methods: Protein profiles of the anterior and posterior horn in post-mortem spinal cord samples of 10 ALS patients and 10 controls were analysed using 2D-differential gel electrophoresis. The identified protein spots with statistically significant level changes and a spot ratio >2.0 were analysed by LC-MS/MS. Results: In the posterior horn only 3 proteins were differentially expressed. In the anterior horn, 16 proteins with increased levels and 2 proteins with decreased levels were identified in ALS compared to controls. The identified proteins were involved in mitochondrial metabolism, calcium homeostasis, protein metabolism, glutathione homeostasis, protein transport and snRNP assembly. The two proteins with decreased levels, ATP5D and calmodulin, were validated by Western blot and immunostaining. Immunohistochemical and immunofluorescent double staining of ATP5D and synaptophysin showed that the reduction of ATP5D was most pronounced at synapses. Conclusions: We speculate that mitochondrial dysfunction in synaptic clefts could play an important role in sALS pathogenesis. A similar approach revealed decreased calmodulin expression mainly in the neuronal body and dendrites of ALS patients. These findings contribute to a deeper understanding of the disease process underlying ALS.
KW - Amyotrophic lateral sclerosis
KW - ATP5D
KW - proteomics
KW - spinal cord
KW - synaptic mitochondrial defect
KW - Two-Dimensional Differential Gel Electrophoresis (2D-DIGE)
UR - http://www.scopus.com/inward/record.url?scp=84999791876&partnerID=8YFLogxK
U2 - 10.1080/21678421.2016.1245757
DO - 10.1080/21678421.2016.1245757
M3 - Article
C2 - 27899032
SN - 2167-8421
VL - 18
SP - 210
EP - 220
JO - Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
JF - Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
IS - 3-4
ER -