Differentiation capacity of dental pulp stem cell into inner ear hair cell using an in vitro assay: a preliminary step toward treating sensorineural hearing loss
Autor: | Farhat, Ferry Sandra, C.R. Sartika, Indri Adriztina, Rosita Juwita Sembiring, Imam Budi Putra, Endah Dianty Pratiwi, Angliana Chouw, Jenny Bashiruddin, Muhamad Ichwan, Delfitri Munir |
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Rok vydání: | 2021 |
Předmět: |
Cell type
Hearing Loss Sensorineural medicine.medical_treatment Basic fibroblast growth factor 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine stomatognathic system Dental pulp stem cells Hair Cells Auditory otorhinolaryngologic diseases medicine Humans 030223 otorhinolaryngology Dental Pulp Epidermal Growth Factor business.industry Stem Cells Cell Differentiation General Medicine Stem-cell therapy medicine.disease Cell biology Neuroepithelial cell medicine.anatomical_structure Otorhinolaryngology chemistry 030220 oncology & carcinogenesis Sensorineural hearing loss sense organs Hair cell Stem cell business |
Zdroj: | European Archives of Oto-Rhino-Laryngology. 279:1805-1812 |
ISSN: | 1434-4726 0937-4477 |
Popis: | Sensorineural hearing loss (SNHL) is commonly caused by the death or dysfunction of cochlear cell types as a result of their lack of regenerative capacity. However, regenerative medicine, such as stem cell therapy, has become a promising tool to cure many diseases, including hearing loss. In this study, we determined whether DPSCs could differentiate into cochlear hair cell in vitro. DPSCs derived from human third molar dental pulp were induced into NSCs using a medium containing basic fibroblast growth factor (bFGF) and epidermal growth factor (EGF) for 7 days, and then into cochlear hair cell using a medium containing EGF and IGF-1 for the next 14 days. We used the neuroepithelial protein marker nestin and cochlear hair cell marker myosin VIIa as the markers for cells differentiation. Cells expressing the positive markers under the microscope were confirmed to have differentiated into cochlear hair cell. DPSCs were successfully induced to differentiate into NSCs, with mean 24% nestin-positive cells. We found that DPSC-derived NSCs have a great capacity in differentiating into inner ear hair cell-like cells with an average of 81% cells presenting myosin VIIa. Thus, DPSCs have high potential to serve as a good resource for SNHL treatment. We found the high potential of DPSCs to differentiate into NSC. The ability of DPSCs in differentiating into neural lineage cell made them a good candidate for regenerative therapy in neural diseases, such as SNHL |
Databáze: | OpenAIRE |
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