Histone deacetylase inhibitors increase neuronal differentiation in adult forebrain precursor cells

Chromatin modification plays a key role in fate decision of neural stem cells. Here, we explored the impact of epigenetic remodelling onto neuronal fate determination using specific inhibitors of histone deacetylases (iHDAC). Adult subventricular zone (SVZ) precursor cells were expanded as neurosphe...

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Published inExperimental brain research Vol. 176; no. 4; pp. 672 - 678
Main Authors Siebzehnrubl, Florian A., Buslei, Rolf, Eyupoglu, Ilker Y., Seufert, Sebastian, Hahnen, Eric, Blumcke, Ingmar
Format Journal Article
LanguageEnglish
Published Berlin Springer 01.02.2007
Springer Nature B.V
Subjects
Online AccessGet full text
ISSN0014-4819
1432-1106
DOI10.1007/s00221-006-0831-x

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Abstract Chromatin modification plays a key role in fate decision of neural stem cells. Here, we explored the impact of epigenetic remodelling onto neuronal fate determination using specific inhibitors of histone deacetylases (iHDAC). Adult subventricular zone (SVZ) precursor cells were expanded as neurospheres and treated in vitro with second generation iHDAC MS-275, M344 and suberoylanilide hydroxamic acid (SAHA). All tested compounds revealed a significant increase of betaIII-tubulin positive neurons (ranging from 258 to 431%) in a concentration-dependent manner. The number of oligodendrocytes was decreased by almost 50%, accompanied by a reduction of Olig2 mRNA expression. In contrast, astrocyte quantity remained unaffected after iHDAC treatment. Both control and iHDAC treated cells expressed markers of mature GABAergic and dopaminergic neurons. Increased expression levels of NeuroD, Cyclin D2 and B-lymphocyte translocation gene 3 (Btg3) point to a shift towards neuronal fate determination targeted by HDAC inhibitors.
AbstractList Chromatin modification plays a key role in fate decision of neural stem cells. Here, we explored the impact of epigenetic remodelling onto neuronal fate determination using specific inhibitors of histone deacetylases (iHDAC). Adult subventricular zone (SVZ) precursor cells were expanded as neurospheres and treated in vitro with second generation iHDAC MS-275, M344 and suberoylanilide hydroxamic acid (SAHA). All tested compounds revealed a significant increase of betaIII-tubulin positive neurons (ranging from 258 to 431%) in a concentration-dependent manner. The number of oligodendrocytes was decreased by almost 50%, accompanied by a reduction of Olig2 mRNA expression. In contrast, astrocyte quantity remained unaffected after iHDAC treatment. Both control and iHDAC treated cells expressed markers of mature GABAergic and dopaminergic neurons. Increased expression levels of NeuroD, Cyclin D2 and B-lymphocyte translocation gene 3 (Btg3) point to a shift towards neuronal fate determination targeted by HDAC inhibitors.
Chromatin modification plays a key role in fate decision of neural stem cells. Here, we explored the impact of epigenetic remodelling onto neuronal fate determination using specific inhibitors of histone deacetylases (iHDAC). Adult subventricular zone (SVZ) precursor cells were expanded as neurospheres and treated in vitro with second generation iHDAC MS-275, M344 and suberoylanilide hydroxamic acid (SAHA). All tested compounds revealed a significant increase of betaIII-tubulin positive neurons (ranging from 258 to 431%) in a concentration-dependent manner. The number of oligodendrocytes was decreased by almost 50%, accompanied by a reduction of Olig2 mRNA expression. In contrast, astrocyte quantity remained unaffected after iHDAC treatment. Both control and iHDAC treated cells expressed markers of mature GABAergic and dopaminergic neurons. Increased expression levels of NeuroD, Cyclin D2 and B-lymphocyte translocation gene 3 (Btg3) point to a shift towards neuronal fate determination targeted by HDAC inhibitors.Chromatin modification plays a key role in fate decision of neural stem cells. Here, we explored the impact of epigenetic remodelling onto neuronal fate determination using specific inhibitors of histone deacetylases (iHDAC). Adult subventricular zone (SVZ) precursor cells were expanded as neurospheres and treated in vitro with second generation iHDAC MS-275, M344 and suberoylanilide hydroxamic acid (SAHA). All tested compounds revealed a significant increase of betaIII-tubulin positive neurons (ranging from 258 to 431%) in a concentration-dependent manner. The number of oligodendrocytes was decreased by almost 50%, accompanied by a reduction of Olig2 mRNA expression. In contrast, astrocyte quantity remained unaffected after iHDAC treatment. Both control and iHDAC treated cells expressed markers of mature GABAergic and dopaminergic neurons. Increased expression levels of NeuroD, Cyclin D2 and B-lymphocyte translocation gene 3 (Btg3) point to a shift towards neuronal fate determination targeted by HDAC inhibitors.
Chromatin modification plays a key role in fate decision of neural stem cells. Here, we explored the impact of epigenetic remodelling onto neuronal fate determination using specific inhibitors of histone deacetylases (iHDAC). Adult subventricular zone (SVZ) precursor cells were expanded as neurospheres and treated in vitro with second generation iHDAC MS-275, M344 and suberoylanilide hydroxamic acid (SAHA). All tested compounds revealed a significant increase of beta III-tubulin positive neurons (ranging from 258 to 431%) in a concentration-dependent manner. The number of oligodendrocytes was decreased by almost 50%, accompanied by a reduction of Olig2 mRNA expression. In contrast, astrocyte quantity remained unaffected after iHDAC treatment. Both control and iHDAC treated cells expressed markers of mature GABAergic and dopaminergic neurons. Increased expression levels of NeuroD, Cyclin D2 and B-lymphocyte translocation gene 3 (Btg3) point to a shift towards neuronal fate determination targeted by HDAC inhibitors.
Chromatin modification plays a key role in fate decision of neural stem cells. Here, we explored the impact of epigenetic remodelling onto neuronal fate determination using specific inhibitors of histone deacetylases (iHDAC). Adult subventricular zone (SVZ) precursor cells were expanded as neurospheres and treated in vitro with second generation iHDAC MS-275, M344 and suberoylanilide hydroxamic acid (SAHA). All tested compounds revealed a significant increase of βIII-tubulin positive neurons (ranging from 258 to 431%) in a concentration-dependent manner. The number of oligodendrocytes was decreased by almost 50%, accompanied by a reduction of Olig2 mRNA expression. In contrast, astrocyte quantity remained unaffected after iHDAC treatment. Both control and iHDAC treated cells expressed markers of mature GABAergic and dopaminergic neurons. Increased expression levels of NeuroD, Cyclin D2 and B-lymphocyte translocation gene 3 (Btg3) point to a shift towards neuronal fate determination targeted by HDAC inhibitors.
Author Buslei, Rolf
Eyupoglu, Ilker Y.
Siebzehnrubl, Florian A.
Hahnen, Eric
Seufert, Sebastian
Blumcke, Ingmar
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  surname: Eyupoglu
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  surname: Seufert
  fullname: Seufert, Sebastian
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  surname: Hahnen
  fullname: Hahnen, Eric
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  givenname: Ingmar
  surname: Blumcke
  fullname: Blumcke, Ingmar
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IsScholarly true
Issue 4
Keywords HDAC· Adult stem cells
Stem cell
Precursor cell
Neurospheres
Dopaminergic neuron
Acetylation
Differentiation
Gabaergic neuron
Language English
License CC BY 4.0
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Springer Nature B.V
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Snippet Chromatin modification plays a key role in fate decision of neural stem cells. Here, we explored the impact of epigenetic remodelling onto neuronal fate...
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SubjectTerms Age Factors
Animals
Animals, Newborn
Basic Helix-Loop-Helix Transcription Factors - genetics
Biological and medical sciences
Biomarkers - metabolism
Cell cycle
Cell death
Cell differentiation
Cell Differentiation - drug effects
Cell Differentiation - physiology
Cell Proliferation - drug effects
Cells, Cultured
Chromatin
Cyclin D2
Dopamine - metabolism
Dopamine D2 receptors
Dose-Response Relationship, Drug
Enzyme Inhibitors - pharmacology
Enzymes
Epigenesis, Genetic - drug effects
Epigenesis, Genetic - genetics
Epigenetics
Forebrain
Fundamental and applied biological sciences. Psychology
gamma-Aminobutyric Acid - metabolism
Gene expression
Histone deacetylase
Histone Deacetylase Inhibitors
Histone Deacetylases - metabolism
Hydroxamic acid
Isolated neuron and nerve. Neuroglia
Lymphocytes B
Motor control and motor pathways. Reflexes. Control centers of vegetative functions. Vestibular system and equilibration
Nerve Tissue Proteins - genetics
Nerve Tissue Proteins - metabolism
Neural stem cells
NeuroD protein
Neurons
Neurons - cytology
Neurons - drug effects
Neurons - enzymology
Neurospheres
Olig2 protein
Oligodendrocyte Transcription Factor 2
Oligodendrocytes
Oligodendroglia - drug effects
Oligodendroglia - metabolism
Prosencephalon - cytology
Prosencephalon - drug effects
Prosencephalon - enzymology
Rats
Rats, Wistar
Spheres
Spheroids, Cellular
Stem cells
Stem Cells - cytology
Stem Cells - drug effects
Stem Cells - enzymology
Subventricular zone
Tubulin
Tubulin - drug effects
Tubulin - metabolism
Vertebrates: nervous system and sense organs
γ-Aminobutyric acid
Title Histone deacetylase inhibitors increase neuronal differentiation in adult forebrain precursor cells
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Volume 176
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