2.Stem Cell-Based Hair Cell Regeneration and Therapy in the Inner Ear.
Jieyu QI ; Wenjuan HUANG ; Yicheng LU ; Xuehan YANG ; Yinyi ZHOU ; Tian CHEN ; Xiaohan WANG ; Yafeng YU ; Jia-Qiang SUN ; Renjie CHAI
Neuroscience Bulletin 2024;40(1):113-126
Hearing loss has become increasingly prevalent and causes considerable disability, thus gravely burdening the global economy. Irreversible loss of hair cells is a main cause of sensorineural hearing loss, and currently, the only relatively effective clinical treatments are limited to digital hearing equipment like cochlear implants and hearing aids, but these are of limited benefit in patients. It is therefore urgent to understand the mechanisms of damage repair in order to develop new neuroprotective strategies. At present, how to promote the regeneration of functional hair cells is a key scientific question in the field of hearing research. Multiple signaling pathways and transcriptional factors trigger the activation of hair cell progenitors and ensure the maturation of newborn hair cells, and in this article, we first review the principal mechanisms underlying hair cell reproduction. We then further discuss therapeutic strategies involving the co-regulation of multiple signaling pathways in order to induce effective functional hair cell regeneration after degeneration, and we summarize current achievements in hair cell regeneration. Lastly, we discuss potential future approaches, such as small molecule drugs and gene therapy, which might be applied for regenerating functional hair cells in the clinic.
Infant, Newborn
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Humans
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Hair Cells, Auditory, Inner/physiology*
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Ear, Inner/physiology*
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Hair Cells, Auditory/physiology*
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Regeneration/genetics*
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Stem Cells
6.Valuation of Transient Evoked Otoacoustic Emissions and Distortion Product Otoacoustic Emissions in Tinnitus Patients with Normal Hearing.
Jeong Tae KIM ; Hyun Soo LEE ; Hye Ran LEE ; Ho Seok CHOI ; Byung Don LEE ; Kyurin HWANG
Korean Journal of Otolaryngology - Head and Neck Surgery 2016;59(12):831-835
BACKGROUND AND OBJECTIVES: This study aims to verify that one of the causes of tinnitus is the malfunction of outer hair cells and, on the basis of this, to investigate the usefulness of otoacoustic emissions by performing transient evoked otoacoustic emissions (TEOAE) and distor-tion product otoacoustic emissions (DPOAE). SUBJECTS AND METHOD: Included in the study were forty-one patients who had normal hearing in the range from 0.5 to 8 kHz, and complained of unilateral tinnitus. In these patients, hearing in bilateral ears, TEOAE, DPOAE, as well as the frequency & amplitude of their tinnitus were measured. RESULTS: No statistically significant difference was found in bilateral hearing in patients who complained of unilateral tinnitus. However, TEOAE and DPOAE showed a statistically significant difference with their p-values at 0.04 and 0.004, respectively. CONCLUSION: The results of this study suggested that TEOAE testing and DPOAE testing provide an important clue for verifying that the loss of outer hair cells contributed to the development of symptoms suffered by tinnitus patients with normal hearing.
Ear
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Hair Cells, Auditory, Outer
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Hearing*
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Humans
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Methods
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Tinnitus*
7.Dynamic changes in hair cell ribbon synapse induced by loss of spiral ganglion neurons in mice.
Chinese Medical Journal 2014;127(10):1941-1946
BACKGROUNDPrevious studies have suggested that primary degeneration of hair cells causes secondary degeneration of spiral ganglion neurons (SGNs), but the effect of SGN degeneration on hair cells has not been studied. In the adult mouse inner ear ouabain can selectively and permanently induce the degeneration of type 1 SGNs while leaving type 2 SGNs, efferent fibers, and sensory hair cells relatively intact. This study aimed to investigate the dynamic changes in hair cell ribbon synapse induced by loss of SGNs using ouabain application to the round window niche of adult mice.
METHODSIn the analysis, 24 CBA/CAJ mice aged 8-10 weeks, were used, of which 6 normal mice were used as the control group. After ouabain application in the round window niche 6 times in an hour, ABR threshold shifts at least 30 dB in the three experimental groups which had six mice for 1-week group, six for 1-month group, and six for 3-month group. All 24 animals underwent function test at 1 week and then immunostaining at 1 week, 1 month, and 3 months.
RESULTSThe loss of neurons was followed by degeneration of postsynaptic specializations at the afferent synapse with hair cells. One week after ouabain treatment, the nerve endings of type 1 SGNs and postsynaptic densities, as measured by Na/K ATPase and PSD-95, were affected but not entirely missing, but their partial loss had consequences for synaptic ribbons that form the presynaptic specialization at the synapse between hair cells and primary afferent neurons. Ribbon numbers in inner hair cells decreased (some of them broken and the ribbon number much decreased), and the arrangement of the synaptic ribbons had undergone a dynamic reorganization: ribbons with or without associated postsynaptic densities moved from their normal location in the basal membrane of the cell to a more apical location and the neural endings alone were also found at more apical locations without associated ribbons. After 1 month, when the neural postsynaptic densities had completed their degeneration, most ribbons were lost and the remaining ribbons had no contact with postsynaptic densities; after 3 months, the ribbon synapses were gone except for an occasional remnant of a CtBP2-positive vesicle. Hair cells were intact other than the loss of ribbons (based on immunohistochemistry and DPOAE).
CONCLUSIONThese findings define the effect of SGN loss on the precise spatiotemporal size and location of ribbons and the time course of synaptic degeneration and provide a model for studying plasticity and regeneration.
Animals ; Female ; Hair Cells, Auditory ; cytology ; physiology ; Hair Cells, Auditory, Inner ; cytology ; physiology ; Mice ; Mice, Inbred CBA ; Synapses ; physiology
8.The expression and significance of adaptin-2 in mice cochlea.
Xiang GU ; Rui SONG ; Zhiji CHEN ; Wei YUAN
Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2015;29(1):83-85
OBJECTIVE:
To investigate the expression of adaptin-2(AP-2) in mice cochlea and to discuss the probable role in the endocytosis of hair cells.
METHOD:
Laser scanning confocal microscopy and immune-fluroscence histochemistry were performed in this study.
RESULT:
In mature mice cochlea, the immunoreactivity for AP-2 was found in the inner hair cells cytoplasm. This protein mainly expressed in the hair cells basal part and nearby the ribbon synapse.
CONCLUSION
AP-2 protein mainly expressed in the hair cells synaptic activity zone , which suggested that AP-2 could play an important role in the synaptic vesicle endocytosis. This finding built the foundation for the further research involved in the physiological and pathological role of AP-2.
Adaptor Protein Complex alpha Subunits
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metabolism
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Animals
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Cochlea
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Hair Cells, Auditory
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Hair Cells, Auditory, Inner
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metabolism
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Mice
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Microscopy, Confocal
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Synapses
9.Atoh1 as a Coordinator of Sensory Hair Cell Development and Regeneration in the Cochlea
Sungsu LEE ; Han Seong JEONG ; Hyong Ho CHO
Chonnam Medical Journal 2017;53(1):37-46
Cochlear sensory hair cells (HCs) are crucial for hearing as mechanoreceptors of the auditory systems. Clarification of transcriptional regulation for the cochlear sensory HC development is crucial for the improvement of cell replacement therapies for hearing loss. Transcription factor Atoh1 is the key player during HC development and regeneration. In this review, we will focus on Atoh1 and its related signaling pathways (Notch, fibroblast growth factor, and Wnt/β-catenin signaling) involved in the development of cochlear sensory HCs. We will also discuss the potential applicability of these signals for the induction of HC regeneration.
Cochlea
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Fibroblast Growth Factors
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Hair Cells, Auditory
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Hair
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Hearing
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Hearing Loss
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Mechanoreceptors
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Regeneration
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Transcription Factors
10.Investigation on degeneration of outer hair cells in guinea pig.
Xixun KANG ; Weijia KONG ; Wanrong LI ; Xiaorong ZENG ; Song ZHNAG ; Changkai GUO ; Xiang HUANG
Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2008;22(23):1087-1089
OBJECTIVE:
To investigate the degeneration mechanics of outer hair cells in guinea pig.
METHOD:
The mechanics of outer hair cells isolated by enzyme were observed under inverted microscope for 6-8 h continuously.
RESULT:
Over half of living outer hair cells could keep good conditions in 6 hours. During the degeneration there was always a longitudinal fold line from tip to base. Presence or absence of calcium, as well as lossing of stereociliary bundle, couldn't change the conditions of out hair cells.
CONCLUSION
Neither calcium nor stereociliary bundle is the decisive cause in keeping outer hair cells alive, and its degeneration may be basically related with something surrounding the cell.
Animals
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Calcium
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Cells, Cultured
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Cochlea
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cytology
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pathology
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Culture Media
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Guinea Pigs
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Hair Cells, Auditory
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cytology