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Basic Fibroblast Growth Factor Induces Cholinergic Differentiation of Tonsil-Derived Mesenchymal Stem Cells

Title
Basic Fibroblast Growth Factor Induces Cholinergic Differentiation of Tonsil-Derived Mesenchymal Stem Cells
Authors
Song J.-H.Oh S.-Y.Jo S.A.
Ewha Authors
오세영
SCOPUS Author ID
오세영scopusscopus
Issue Date
2022
Journal Title
Tissue Engineering and Regenerative Medicine
ISSN
1738-2696JCR Link
Citation
Tissue Engineering and Regenerative Medicine vol. 19, no. 5, pp. 1063 - 1075
Keywords
Basic fibroblast growth factorNeuronal differentiationTonsil-derived mesenchymal stem cells
Publisher
Korean Tissue Engineering and Regenerative Medicine Society
Indexed
SCIE; SCOPUS; KCI WOS scopus
Document Type
Article
Abstract
Background:: Mesenchymal stem cells (MSCs) are considered a potential tool for regenerating damaged tissues due to their great multipotency into various cell types. Here, we attempted to find the appropriate conditions for neuronal differentiation of tonsil-derived MSCs (TMSCs) and expand the potential application of TMSCs for treating neurological diseases. Methods:: The TMSCs were differentiated in DMEM/F-12 (Dulbecco's Modified Eagle Medium/Nutrient Mixture F-12) supplemented with various neurotrophic factors for 7–28 days to determine the optimal neuronal differentiation condition for the TMSCs. The morphologies as well as the levels of the neural markers and neurotransmitters were assessed to determine neuronal differentiation potentials and the neuronal lineages of the differentiated TMSCs. Results:: Our initial study demonstrated that DMEM/F12 supplemented with 50 ng/mL basic fibroblast growth factor with 10 μM forskolin was the optimal condition for neuronal differentiation for the TMSCs. TMSCs had higher protein expression of neuronal markers, including neuron-specific enolase (NSE), GAP43, postsynaptic density protein 95 (PSD95), and synaptosomal-associated protein of 25 kDa (SNAP25) compared to the undifferentiated TMSCs. Immunofluorescence staining also validated the increased mature neuron markers, NeuN and synaptophysin, in the differentiated TMSCs. The expression of glial fibrillar acidic protein and ionized calcium-binding adaptor molecule 1 the markers of astrocytes and microglia, were also slightly increased. Additionally, the differentiated TMSCs released a significantly higher level of acetylcholine, the cholinergic neurotransmitter, as analyzed by the liquid chromatography-tandem mass spectrometry and showed an enhanced choline acetyltransferase immunoreactivity compared to the undifferentiated cells. Conclusion:: Our study suggests that the optimized condition favors the TMSCs to differentiate into cholinergic neuron-like phenotype, which could be used as a possible therapeutic tool in treating certain neurological disorders such as Alzheimer’s disease. © 2022, Korean Tissue Engineering and Regenerative Medicine Society.
DOI
10.1007/s13770-022-00474-0
Appears in Collections:
연구기관 > 의과학연구소 > Journal papers
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