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dc.contributor.authorFahsai Kantawongen_US
dc.contributor.authorChanidapa Saksiriwisitkulen_US
dc.contributor.authorChanakan Riyapaen_US
dc.contributor.authorSuchalinee Limpakdeeen_US
dc.contributor.authorPhenphichar Wanachantararaken_US
dc.contributor.authorThasaneeya Kubokien_US
dc.date.accessioned2018-09-05T04:22:44Z-
dc.date.available2018-09-05T04:22:44Z-
dc.date.issued2018-01-01en_US
dc.identifier.issn22285660en_US
dc.identifier.issn22285652en_US
dc.identifier.other2-s2.0-85048143913en_US
dc.identifier.other10.15171/bi.2018.15en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85048143913&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/58324-
dc.description.abstract© 2018 The Author(s). Introduction: Induced neural stem cells (iNSCs) have the ability of differentiation into neurons, astrocytes and oligodendrocytes. iNSCs are very useful in terms of research and treatment. The present study offers an idea that biomaterials could be one of the tools that could modulate reprogramming process in the fibroblasts. Methods: Gelatin biomaterials were fabricated into 3 types, including (i) gelatin, (ii) gelatin with 1 mg/mL hydroxyapatite, and (iii) gelatin with hydroxyapatite and pig brain. NIH/3T3 fibroblasts were cultured on each type of biomaterial for 7, 9 and 14 days. RT-PCR was performed to investigate the gene expression of the fibroblasts on biomaterials compared to the fibroblasts on tissue culture plates. PI3K/Akt signaling was performed by flow cytometry after 24 hours seeding on the biomaterials. The biomaterials were also tested with the human APCs and PDL cells. Results: The fibroblasts exhibited changes in the expression of the reprogramming factor; Klf 4 and the neural transcription factors; NFIa, NFIb and Ptbp1 after 9 days culture. The cultivation of fibroblasts on the biomaterials for 7 days showed a higher expression of the transcription factor SOX9. The expression of epigenetic genes; Kat2a and HDAC3 were changed upon the cultivation on the biomaterials for 9 days. The fibroblasts cultured on the biomaterials showed an activation of PI3K/Akt signaling. The human APCs and human PDL cells developed mineralization process on biomaterials. Conclusion: Changes in the expression of Klf4, NFIa, NFIb, Ptbp1 and SOX9 indicated that fibroblasts were differentiated into an astrocytic lineage. It is possible that the well-designed biomaterials could work as powerful tools in the reprogramming process of fibroblasts into iNSCs.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleReprogramming of mouse fibroblasts into neural lineage cells using biomaterialsen_US
dc.typeJournalen_US
article.title.sourcetitleBioImpactsen_US
article.volume8en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsKyushu Universityen_US
Appears in Collections:CMUL: Journal Articles

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