CC BY 4.0 · Eur J Dent 2023; 17(04): 1207-1214
DOI: 10.1055/s-0043-1761190
Original Article

Evaluation of the Efficacy of Human Dental Pulp Stem Cell Transplantation in Sprague–Dawley Rats with Sensorial Neural Hearing Loss

Visut Rawiwet
1   Central Animal Facility, Faculty of Science, Mahidol University (MUSC-CAF), Bangkok, Thailand
,
Rattanavijit Vijitruth
2   Department of Biology, Faculty of Science, Mahidol University, Bangkok, Thailand
,
Chareonsri Thonabulsombat
3   Department of Anatomy, Faculty of Science, Mahidol University, Bangkok, Thailand
,
Kutkao Vongsavan
4   Department of Pediatric Dentistry, Faculty of Dentistry, Mahidol University, Bangkok, Thailand
,
Hathaitip Sritanaudomchai
5   Department of Oral Biology, Faculty of Dentistry, Mahidol University, Bangkok, Thailand
› Author Affiliations

Abstract

Objectives The purpose of the present study was to evaluate the efficacy of spiral ganglion neuron (SGN) regeneration after dental pulp stem cell (DPSC) transplantation in a rat sensorineural hearing loss (HL) model.

Materials and Methods Sham or experimental HL was induced in adult Sprague–Dawley rats by cochlear round window surgery. An HL rat model was established with a single 10 mM ouabain intratympanic injection. After 7 days, the rats received DPSCs, stem cells from human exfoliated deciduous teeth (SHED), or culture medium in the sutural area to establish four groups: sham, HL-DPSC, HL-SHED, and HL-medium. Histological analyses were performed at 4, 7, and 10 weeks after transplantation, and the number of SGNs, specific SGN protein expression, and the function of SGNs were evaluated.

Statistical Analysis Data were statistically by MS Excel and SPSS v.15.0. Intergroup level of significance was determined via a one-way analysis of variance and Duncan's multiple range test with 95% confidence intervals.

Results New SGN formation was observed in the HL-DPSC and HL-SHED rat groups. The number of SGNs was significantly higher in the HL-DPSC and HL-SHED groups than in the HL-medium group over 4 to 10-week survival period. HL-DPSC rats exhibited higher SGN density compared with that in HL-SHED group, which was statistically significant at week 10. The regenerated SGNs expressed cochlear wiring regulator GATA-binding-protein 3. Moreover, the SGNs from the HL-DPSC group also exhibited a higher expression of synaptic vesicle protein and regulated action potential-dependent neurotransmitter release compared with SGNs from the HL-SHED group.

Conclusions Our findings suggest that DPSCs and SHED repair and regenerate SGNs in rat HL model. Dental pulp stem cells represent a promising treatment strategy for restoring damage to the sensory circuits associated with deafness.



Publication History

Article published online:
30 January 2023

© 2023. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)

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  • References

  • 1 Thusi AB, Paken J. The lived experiences and psychosocial impact of hearing loss on the quality of life of adults with multidrug-resistant tuberculosis. S Afr J Commun Disord 2022; 69 (01) e1-e13
  • 2 Vlastarakos PV, Nikolopoulos TP, Tavoulari E, Papacharalambous G, Korres S. Auditory neuropathy: endocochlear lesion or temporal processing impairment? Implications for diagnosis and management. Int J Pediatr Otorhinolaryngol 2008; 72 (08) 1135-1150
  • 3 Chen W, Jongkamonwiwat N, Abbas L. et al. Restoration of auditory evoked responses by human ES-cell-derived otic progenitors. Nature 2012; 490 (7419): 278-282
  • 4 Corrales CE, Pan L, Li H, Liberman MC, Heller S, Edge AS. Engraftment and differentiation of embryonic stem cell-derived neural progenitor cells in the cochlear nerve trunk: growth of processes into the organ of Corti. J Neurobiol 2006; 66 (13) 1489-1500
  • 5 Lang H, Schulte BA, Goddard JC. et al. Transplantation of mouse embryonic stem cells into the cochlea of an auditory-neuropathy animal model: effects of timing after injury. J Assoc Res Otolaryngol 2008; 9 (02) 225-240
  • 6 Okano T, Nakagawa T, Endo T. et al. Engraftment of embryonic stem cell-derived neurons into the cochlear modiolus. Neuroreport 2005; 16 (17) 1919-1922
  • 7 Praetorius M, Vicario I, Schimmang T. Efficient transfer of embryonic stem cells into the cochlea via a non-invasive vestibular route. Acta Otolaryngol 2008; 128 (07) 720-723
  • 8 Tan BT, Lee MM, Ruan R. Bone-marrow-derived cells that home to acoustic deafened cochlea preserved their hematopoietic identity. J Comp Neurol 2008; 509 (02) 167-179
  • 9 Arora V, Arora P, Munshi AK. Banking stem cells from human exfoliated deciduous teeth (SHED): saving for the future. J Clin Pediatr Dent 2009; 33 (04) 289-294
  • 10 Huang GT, Gronthos S, Shi S. Mesenchymal stem cells derived from dental tissues vs. those from other sources: their biology and role in regenerative medicine. J Dent Res 2009; 88 (09) 792-806
  • 11 Kawashima N. Characterisation of dental pulp stem cells: a new horizon for tissue regeneration?. Arch Oral Biol 2012; 57 (11) 1439-1458
  • 12 Gonmanee T, Thonabulsombat C, Vongsavan K, Sritanaudomchai H. Differentiation of stem cells from human deciduous and permanent teeth into spiral ganglion neuron-like cells. Arch Oral Biol 2018; 88: 34-41
  • 13 Gonmanee T, Sritanaudomchai H, Vongsavan K. et al. Neuronal differentiation of dental pulp stem cells from human permanent and deciduous teeth following coculture with rat auditory brainstem slices. Anat Rec (Hoboken) 2020; 303 (11) 2931-2946
  • 14 Tangjit N, Dechkunakorn S, Anuwongnukroh N, Khaneungthong A, Sritanaudomchai H. Optimal Xeno-free culture condition for clinical grade stem cells from human exfoliated deciduous teeth. Int J Stem Cells 2018; 11 (01) 96-104
  • 15 Passier R, Mummery C. Origin and use of embryonic and adult stem cells in differentiation and tissue repair. Cardiovasc Res 2003; 58 (02) 324-335
  • 16 Ueda T, Inden M, Ito T, Kurita H, Hozumi I. Characteristics and therapeutic potential of dental pulp stem cells on neurodegenerative diseases. Front Neurosci 2020; 14: 407
  • 17 Coleman B, Hardman J, Coco A. et al. Fate of embryonic stem cells transplanted into the deafened mammalian cochlea. Cell Transplant 2006; 15 (05) 369-380
  • 18 Mead B, Logan A, Berry M, Leadbeater W, Scheven BA. Intravitreally transplanted dental pulp stem cells promote neuroprotection and axon regeneration of retinal ganglion cells after optic nerve injury. Invest Ophthalmol Vis Sci 2013; 54 (12) 7544-7556
  • 19 Ahmed Nel-M, Murakami M, Hirose Y, Nakashima M. Therapeutic potential of dental pulp stem cell secretome for Alzheimer's disease treatment: an in vitro study. Stem Cells Int 2016; 2016: 8102478
  • 20 Zhang J, Lu X, Feng G. et al. Chitosan scaffolds induce human dental pulp stem cells to neural differentiation: potential roles for spinal cord injury therapy. Cell Tissue Res 2016; 366 (01) 129-142
  • 21 Mita T, Furukawa-Hibi Y, Takeuchi H. et al. Conditioned medium from the stem cells of human dental pulp improves cognitive function in a mouse model of Alzheimer's disease. Behav Brain Res 2015; 293: 189-197
  • 22 Apel C, Forlenza OV, de Paula VJ. et al. The neuroprotective effect of dental pulp cells in models of Alzheimer's and Parkinson's disease. J Neural Transm (Vienna) 2009; 116 (01) 71-78
  • 23 Zhang N, Lu X, Wu S. et al. Intrastriatal transplantation of stem cells from human exfoliated deciduous teeth reduces motor defects in Parkinsonian rats. Cytotherapy 2018; 20 (05) 670-686
  • 24 Wang L, Zhao Y, Shi S. Interplay between mesenchymal stem cells and lymphocytes: implications for immunotherapy and tissue regeneration. J Dent Res 2012; 91 (11) 1003-1010
  • 25 Király M, Porcsalmy B, Pataki A. et al. Simultaneous PKC and cAMP activation induces differentiation of human dental pulp stem cells into functionally active neurons. Neurochem Int 2009; 55 (05) 323-332
  • 26 Arthur A, Rychkov G, Shi S, Koblar SA, Gronthos S. Adult human dental pulp stem cells differentiate toward functionally active neurons under appropriate environmental cues. Stem Cells 2008; 26 (07) 1787-1795
  • 27 Kang CM, Shin MK, Jeon M, Lee YH, Song JS, Lee JH. Distinctive cytokine profiles of stem cells from human exfoliated deciduous teeth and dental pulp stem cells. J Dent Sci 2022; 17 (01) 276-283