Stem cell-based approaches: Possible route to hearing restoration?
Disabling hearing loss is the most common sensorineural disability worldwide. It affects around 466 million people and its incidence is expected to rise to around 900 million people by 2050, according to World Health Organization estimates. Most cases of hearing impairment are due to the degeneratio...
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Published in | World journal of stem cells Vol. 12; no. 6; pp. 422 - 437 |
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Language | English |
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Baishideng Publishing Group Inc
26.06.2020
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Abstract | Disabling hearing loss is the most common sensorineural disability worldwide. It affects around 466 million people and its incidence is expected to rise to around 900 million people by 2050, according to World Health Organization estimates. Most cases of hearing impairment are due to the degeneration of hair cells (HCs) in the cochlea, mechano-receptors that transduce incoming sound information into electrical signals that are sent to the brain. Damage to these cells is mainly caused by exposure to aminoglycoside antibiotics and to some anti-cancer drugs such as cisplatin, loud sounds, age, infections and genetic mutations. Hearing deficits may also result from damage to the spiral ganglion neurons that innervate cochlear HCs. Differently from what is observed in avian and non-mammalian species, there is no regeneration of missing sensory cell types in the adult mammalian cochlea, what makes hearing loss an irreversible process. This review summarizes the research that has been conducted with the aim of developing cell-based strategies that lead to sensory cell replacement in the adult cochlea and, ultimately, to hearing restoration. Two main lines of research are discussed, one directed toward the transplantation of exogenous replacement cells into the damaged tissue, and another that aims at reactivating the regenerative potential of putative progenitor cells in the adult inner ear. Results from some of the studies that have been conducted are presented and the advantages and drawbacks of the various approaches discussed.Disabling hearing loss is the most common sensorineural disability worldwide. It affects around 466 million people and its incidence is expected to rise to around 900 million people by 2050, according to World Health Organization estimates. Most cases of hearing impairment are due to the degeneration of hair cells (HCs) in the cochlea, mechano-receptors that transduce incoming sound information into electrical signals that are sent to the brain. Damage to these cells is mainly caused by exposure to aminoglycoside antibiotics and to some anti-cancer drugs such as cisplatin, loud sounds, age, infections and genetic mutations. Hearing deficits may also result from damage to the spiral ganglion neurons that innervate cochlear HCs. Differently from what is observed in avian and non-mammalian species, there is no regeneration of missing sensory cell types in the adult mammalian cochlea, what makes hearing loss an irreversible process. This review summarizes the research that has been conducted with the aim of developing cell-based strategies that lead to sensory cell replacement in the adult cochlea and, ultimately, to hearing restoration. Two main lines of research are discussed, one directed toward the transplantation of exogenous replacement cells into the damaged tissue, and another that aims at reactivating the regenerative potential of putative progenitor cells in the adult inner ear. Results from some of the studies that have been conducted are presented and the advantages and drawbacks of the various approaches discussed. |
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AbstractList | Disabling hearing loss is the most common sensorineural disability worldwide. It affects around 466 million people and its incidence is expected to rise to around 900 million people by 2050, according to World Health Organization estimates. Most cases of hearing impairment are due to the degeneration of hair cells (HCs) in the cochlea, mechano-receptors that transduce incoming sound information into electrical signals that are sent to the brain. Damage to these cells is mainly caused by exposure to aminoglycoside antibiotics and to some anti-cancer drugs such as cisplatin, loud sounds, age, infections and genetic mutations. Hearing deficits may also result from damage to the spiral ganglion neurons that innervate cochlear HCs. Differently from what is observed in avian and non-mammalian species, there is no regeneration of missing sensory cell types in the adult mammalian cochlea, what makes hearing loss an irreversible process. This review summarizes the research that has been conducted with the aim of developing cell-based strategies that lead to sensory cell replacement in the adult cochlea and, ultimately, to hearing restoration. Two main lines of research are discussed, one directed toward the transplantation of exogenous replacement cells into the damaged tissue, and another that aims at reactivating the regenerative potential of putative progenitor cells in the adult inner ear. Results from some of the studies that have been conducted are presented and the advantages and drawbacks of the various approaches discussed. Disabling hearing loss is the most common sensorineural disability worldwide. It affects around 466 million people and its incidence is expected to rise to around 900 million people by 2050, according to World Health Organization estimates. Most cases of hearing impairment are due to the degeneration of hair cells (HCs) in the cochlea, mechano-receptors that transduce incoming sound information into electrical signals that are sent to the brain. Damage to these cells is mainly caused by exposure to aminoglycoside antibiotics and to some anti-cancer drugs such as cisplatin, loud sounds, age, infections and genetic mutations. Hearing deficits may also result from damage to the spiral ganglion neurons that innervate cochlear HCs. Differently from what is observed in avian and non-mammalian species, there is no regeneration of missing sensory cell types in the adult mammalian cochlea, what makes hearing loss an irreversible process. This review summarizes the research that has been conducted with the aim of developing cell-based strategies that lead to sensory cell replacement in the adult cochlea and, ultimately, to hearing restoration. Two main lines of research are discussed, one directed toward the transplantation of exogenous replacement cells into the damaged tissue, and another that aims at reactivating the regenerative potential of putative progenitor cells in the adult inner ear. Results from some of the studies that have been conducted are presented and the advantages and drawbacks of the various approaches discussed.Disabling hearing loss is the most common sensorineural disability worldwide. It affects around 466 million people and its incidence is expected to rise to around 900 million people by 2050, according to World Health Organization estimates. Most cases of hearing impairment are due to the degeneration of hair cells (HCs) in the cochlea, mechano-receptors that transduce incoming sound information into electrical signals that are sent to the brain. Damage to these cells is mainly caused by exposure to aminoglycoside antibiotics and to some anti-cancer drugs such as cisplatin, loud sounds, age, infections and genetic mutations. Hearing deficits may also result from damage to the spiral ganglion neurons that innervate cochlear HCs. Differently from what is observed in avian and non-mammalian species, there is no regeneration of missing sensory cell types in the adult mammalian cochlea, what makes hearing loss an irreversible process. This review summarizes the research that has been conducted with the aim of developing cell-based strategies that lead to sensory cell replacement in the adult cochlea and, ultimately, to hearing restoration. Two main lines of research are discussed, one directed toward the transplantation of exogenous replacement cells into the damaged tissue, and another that aims at reactivating the regenerative potential of putative progenitor cells in the adult inner ear. Results from some of the studies that have been conducted are presented and the advantages and drawbacks of the various approaches discussed. |
Author | Durán-Alonso, María Beatriz |
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Cites_doi | 10.1016/j.expneurol.2004.12.027 10.1002/term.2072 10.1016/j.ymthe.2019.03.017 10.1242/dev.166579 10.3109/00016489.2013.875220 10.1007/s10162-007-0079-6 10.2217/rme.12.58 10.1038/ncomms11508 10.3389/fnmol.2018.00137 10.3389/fnmol.2018.00452 10.3389/fcell.2019.00014 10.18632/oncotarget.11479 10.1038/s41467-018-06334-7 10.1016/j.mcn.2006.10.003 10.1073/pnas.0808044105 10.1016/j.stemcr.2017.02.003 10.1038/s41419-018-0967-1 10.2217/rme.12.65 10.1002/stem.624 10.1016/j.expneurol.2005.11.006 10.1016/j.brainres.2004.08.013 10.1016/s0925-4773(01)00642-6 10.1073/pnas.1415901112 10.1016/j.ymthe.2019.03.018 10.3727/096368913X669761 10.1097/01.wnr.0000187628.38010.5b 10.1038/nature04849 10.1038/nature25164 10.1016/j.tice.2016.06.011 10.1016/j.yexcr.2004.08.023 10.1002/ar.24065 10.1089/scd.2014.0033 10.1038/nm925 10.1523/JNEUROSCI.0967-15.2015 10.1242/dev.103036 10.1038/nbt.3840 10.1016/j.neulet.2006.12.061 10.1016/j.neulet.2016.01.016 10.1073/pnas.0408239102 10.1523/JNEUROSCI.23-11-04395.2003 10.1634/stemcells.2006-0390 10.1242/dev.119149 10.1097/WNR.0b013e32832ff287 10.1089/scd.2018.0016 10.1371/journal.pone.0162508 10.1038/nm1193 10.1016/j.ydbio.2018.08.013 10.3389/fncel.2017.00409 10.1038/mt.2013.292 10.1016/j.pharmthera.2019.05.003 10.1016/j.heares.2019.107859 10.1073/pnas.1219952110 10.1007/s10162-006-0058-3 10.1002/term.2163 10.3727/096368911X623907 10.3727/000000006783981819 10.1089/scd.2017.0142 10.1007/s00441-019-03018-6 10.2217/rme-2018-0009 10.1111/j.1460-9568.2007.05909.x 10.1089/scd.2013.0274 10.1002/neu.20310 10.3389/fnmol.2017.00426 10.3389/fcell.2019.00025 10.1371/journal.pone.0048544 10.1038/nature11415 10.1155/2018/8137614 10.1002/stem.62 10.1007/s00018-018-2950-5 10.1007/s00441-019-03115-6 10.1242/dev.177188 10.1007/s10162-011-0267-2 10.1038/cddis.2013.230 10.1016/j.gep.2010.08.008 10.1073/pnas.1408064111 10.1073/pnas.1202774109 10.1016/j.heares.2007.06.006 10.1016/j.celrep.2017.01.066 10.1038/nature12298 10.1186/s13287-018-0967-1 10.1016/j.stemcr.2019.05.014 10.1016/j.neulet.2015.05.032 10.1242/dev.087528 10.14670/HH-26.923 10.1016/j.heares.2004.12.005 10.1523/JNEUROSCI.0563-08.2008 10.1038/cddis.2012.56 10.1073/pnas.2334503100 10.1016/j.stemcr.2014.01.008 10.1126/science.284.5421.1837 10.1523/JNEUROSCI.1064-12.2012 10.1371/journal.pone.0200210 10.1016/j.cell.2010.03.035 10.1073/pnas.1605537113 |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 Corresponding author: María Beatriz Durán-Alonso, PhD, Postdoctoral Fellow, Postdoctoral scientist, Institute of Biology and Molecular Genetics, University of Valladolid, C/ Sanz y Forés 3, Valladolid 47003, Spain. mariabeatriz.duran@uva.es Author contributions: Durán-Alonso MB revised the published data and wrote the paper. |
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