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
Purpose 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...
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Published in: | European archives of oto-rhino-laryngology Vol. 279; no. 4; pp. 1805 - 1812 |
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Main Authors: | , , , , , , , , , , |
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Language: | English |
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01-04-2022
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Abstract | Purpose
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.
Methods
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.
Results
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.
Conclusion
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 |
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AbstractList | Purpose
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.
Methods
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.
Results
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.
Conclusion
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 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. PURPOSESensorineural 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. METHODSDPSCs 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. RESULTSDPSCs 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. CONCLUSIONWe 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. |
Author | Sandra, Ferry Bashiruddin, Jenny Adriztina, Indri Putra, Imam Budi Ichwan, Muhamad Sartika, Cynthia Retna Munir, Delfitri Pratiwi, Endah Dianty Farhat Sembiring, Rosita Juwita Chouw, Angliana |
Author_xml | – sequence: 1 givenname: Indri orcidid: 0000-0003-0651-9594 surname: Adriztina fullname: Adriztina, Indri email: adriztina@yahoo.com, indri.adriztina@usu.ac.id organization: Department of Otorhinolaryngology-Head and Neck Surgery, Faculty of Medicine, Universitas Sumatera Utara – sequence: 2 givenname: Delfitri surname: Munir fullname: Munir, Delfitri organization: Department of Otorhinolaryngology-Head and Neck Surgery, Faculty of Medicine, Universitas Sumatera Utara – sequence: 3 givenname: Ferry surname: Sandra fullname: Sandra, Ferry organization: Division of Oral Biology, Departement of Biochemistry and Molecular Biology, Faculty of Dentistry, Trisakti University – sequence: 4 givenname: Muhamad surname: Ichwan fullname: Ichwan, Muhamad organization: Department of Pharmacology and Therapeutics, Faculty of Medicine, Universitas Sumatera Utara – sequence: 5 givenname: Jenny surname: Bashiruddin fullname: Bashiruddin, Jenny organization: Department of Otorhinolaryngology-Head and Neck Surgery, Faculty of Medicine, University of Indonesia – sequence: 6 givenname: Imam Budi surname: Putra fullname: Putra, Imam Budi organization: Department of Dermatovenerology, Faculty of Medicine, Universitas Sumatera Utara – sequence: 7 surname: Farhat fullname: Farhat organization: Department of Otorhinolaryngology-Head and Neck Surgery, Faculty of Medicine, Universitas Sumatera Utara – sequence: 8 givenname: Rosita Juwita surname: Sembiring fullname: Sembiring, Rosita Juwita organization: Department of Clinical Pathology, Faculty of Medicine, Universitas Sumatera Utara – sequence: 9 givenname: Cynthia Retna surname: Sartika fullname: Sartika, Cynthia Retna organization: Prodia Stemcell Indonesia – sequence: 10 givenname: Angliana surname: Chouw fullname: Chouw, Angliana organization: Prodia Stemcell Indonesia – sequence: 11 givenname: Endah Dianty surname: Pratiwi fullname: Pratiwi, Endah Dianty organization: Prodia Stemcell Indonesia |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/34008035$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1590/S0103-64402011000200001 10.2217/rme.13.32 10.1016/j.heares.2007.06.007 10.4252/wjsc.v7.i5.839 10.3109/00016489.2011.603135 10.1159/000486772 10.3727/000000006783981819 10.1016/j.pneurobio.2011.01.004 10.1007/s00418-011-0858-3 10.1007/s10162-005-0012-9 10.1080/14653240600855905 10.1007/s00018-018-2794-z 10.1073/pnas.2334503100 10.1634/stemcells.2006-0390 10.1016/j.drudis.2010.02.006 10.1016/j.archoralbio.2012.08.010 10.1016/j.jfma.2014.09.003 10.1073/pnas.240309797 10.3390/jfb2030249 10.1634/stemcells.2007-0979 10.1038/nprot.2006.33 10.7874/kja.2012.16.2.47 10.1517/14712598.6.9.847 10.1080/000164801317166880 10.1016/S1672-2930(07)50020-6 |
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Keywords | Dental pulp stem cells Sensorineural hearing loss Cochlear hair cell |
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Sensorineural hearing loss (SNHL) is commonly caused by the death or dysfunction of cochlear cell types as a result of their lack of regenerative... 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.... PURPOSESensorineural hearing loss (SNHL) is commonly caused by the death or dysfunction of cochlear cell types as a result of their lack of regenerative... |
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SubjectTerms | Head and Neck Surgery Medicine Medicine & Public Health Neurosurgery Otology Otorhinolaryngology |
Title | 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 |
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