Abstract | BACKGROUND/AIMS: METHODS AND RESULTS: By quantitative real-time PCR, a significant reduction of SIRT1 and SIRT2 was detected in homogenates of the primary motor cortex (white and gray matter), while there were no differences in spinal cord homogenates. When specifically analyzing mRNA and protein expression in the gray matter (cortical layers I-VI of the precentral gyrus, ventral/dorsal horn of the spinal cord) by in situ hybridization histochemistry and immunohistochemistry, we found increased levels of SIRT1, SIRT2 and SIRT5 in ALS which were significant for SIRT1 and SIRT5 mRNA in the spinal cord. CONCLUSION: Our results indicate a general reduction of SIRT1 and SIRT2 in ALS primary motor cortex, while in situ hybridization histochemistry and immunohistochemistry showed neuron-specific upregulation of SIRT1, SIRT2 and SIRT5, particularly in the spinal cord. Opposed effects have been described for SIRT1 and SIRT2: while SIRT1 activation is mainly associated with neuroprotection, SIRT2 upregulation is toxic to neuronal cells. Novel therapeutic approaches in ALS could therefore target SIRT1 activation or SIRT2 inhibition.
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Authors | Sonja Körner, Sebastian Böselt, Nadine Thau, Klaus Jan Rath, Reinhard Dengler, Susanne Petri |
Journal | Neuro-degenerative diseases
(Neurodegener Dis)
Vol. 11
Issue 3
Pg. 141-52
( 2013)
ISSN: 1660-2862 [Electronic] Switzerland |
PMID | 22796962
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2012 S. Karger AG, Basel. |
Chemical References |
- Neuroprotective Agents
- SIRT1 protein, human
- SIRT2 protein, human
- Sirtuin 1
- Sirtuin 2
- Sirtuins
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Topics |
- Adult
- Aged
- Amyotrophic Lateral Sclerosis
(enzymology, pathology, prevention & control)
- Female
- Gene Expression Regulation, Enzymologic
(drug effects)
- Humans
- Male
- Middle Aged
- Motor Cortex
(enzymology, pathology)
- Neuroprotective Agents
(therapeutic use, toxicity)
- Sirtuin 1
(biosynthesis, genetics)
- Sirtuin 2
(biosynthesis, genetics, toxicity)
- Sirtuins
(biosynthesis, genetics, toxicity)
- Spinal Cord
(enzymology, pathology)
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