| Item type: | Article | ||||
|---|---|---|---|---|---|
| Journal or Publication Title: | Glia | ||||
| Publisher: | WILEY-BLACKWELL | ||||
| Place of Publication: | HOBOKEN | ||||
| Volume: | 61 | ||||
| Number of Issue or Book Chapter: | 11 | ||||
| Page Range: | pp. 1767-1783 | ||||
| Date: | 2013 | ||||
| Institutions: | Medicine > Lehrstuhl für Augenheilkunde Medicine > Lehrstuhl für Neurologie | ||||
| Identification Number: |
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| Keywords: | GROWTH-FACTOR-BETA; STEM-CELLS; IN-VITRO; TGF-BETA; INCREASES NEUROGENESIS; STEM/PROGENITOR CELLS; HIPPOCAMPAL-NEURONS; ALZHEIMERS-DISEASE; DENTATE GYRUS; EXPRESSION; adult neural progenitor cells; neuronal excitability; action potential firing; voltage-gated ion channels | ||||
| Dewey Decimal Classification: | 600 Technology > 610 Medical sciences Medicine | ||||
| Status: | Published | ||||
| Refereed: | Yes, this version has been refereed | ||||
| Created at the University of Regensburg: | Yes | ||||
| Item ID: | 62140 |
Web of ScienceAbstract
The differentiation of adult neural progenitors (NPCs) into functional neurons is still a limiting factor in the neural stem cell field but mandatory for the potential use of NPCs in therapeutic approaches. Neuronal function requires the appropriate electrophysiological properties. Here, we demonstrate that priming of NPCs using transforming growth factor (TGF)-1 under conditions that usually ...
Abstract
The differentiation of adult neural progenitors (NPCs) into functional neurons is still a limiting factor in the neural stem cell field but mandatory for the potential use of NPCs in therapeutic approaches. Neuronal function requires the appropriate electrophysiological properties. Here, we demonstrate that priming of NPCs using transforming growth factor (TGF)-1 under conditions that usually favor NPCs' proliferation induces electrophysiological neuronal properties in adult NPCs. Gene chip array analyses revealed upregulation of voltage-dependent ion channel subunits (Kcnd3, Scn1b, Cacng4, and Accn1), neurotransmitters, and synaptic proteins (Cadps, Snap25, Grik4, Gria3, Syngr3, and Gria4) as well as other neuronal proteins (doublecortin [DCX], Nrxn1, Sept8, and Als2cr3). Patch-clamp analysis demonstrated that control-treated cells expressed only voltage-dependent K+-channels of the delayed-rectifier type and the A-type channels. TGF-1-treated cells possessed more negative resting potentials than nontreated cells owing to the presence of delayed-rectifier and inward-rectifier channels. Furthermore, TGF-1-treated cells expressed voltage-dependent, TTX-sensitive Na+ channels, which showed increasing current density with TGF-1 treatment duration and voltage-dependent (+)BayK8644-sensitive L-Type Ca2+ channels. In contrast to nontreated cells, TGF-1-treated cells responded to current injections with action-potentials in the current-clamp mode. Furthermore, TGF-1-treated cells responded to application of GABA with an increase in membrane conductance and showed spontaneous synaptic currents that were blocked by the GABA-receptor antagonist picrotoxine. Only NPCs, which were treated with TGF-1, showed Na+ channel currents, action potentials, and GABAergic currents. In summary, stimulation of NPCs by TGF-1 fosters a functional neuronal phenotype, which will be of relevance for future cell replacement strategies in neurodegenerative diseases or acute CNS lesions. GLIA 2013;61:1767-1783
Metadata last modified: 19 Dec 2024 08:33
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