Development of a nasal mucosa-removal model for evaluating cell therapy.

ADSC, adipose-derived mesenchymal stromal cell Animal models Bone hyperplasia Cell sheet transplantation Chronic rhinosinusitis EDTA, ethylenediaminetetraacetic acid HE, hematoxylin and eosin Maxillary sinus Nasal mucosa regeneration PBS, phosphate-buffered saline POD, postoperative day SEM, standard error of the mean SPF, specific-pathogen-free micro-CT, Micro-computed tomography

Journal

Regenerative therapy
ISSN: 2352-3204
Titre abrégé: Regen Ther
Pays: Netherlands
ID NLM: 101709085

Informations de publication

Date de publication:
Mar 2021
Historique:
received: 02 11 2020
revised: 26 11 2020
accepted: 23 12 2020
entrez: 25 1 2021
pubmed: 26 1 2021
medline: 26 1 2021
Statut: epublish

Résumé

Endoscopic sinus surgery is an effective surgical procedure for treating chronic sinusitis; however, extensive exposure of the bone in the nasal cavity can result in permanent disability postoperatively. Particularly, closure of the sinus drainage pathway due to bone hyperplasia associated with bone exposure can trigger the recurrence of sinusitis. It is essential to regenerate the nasal mucosa after surgery to avoid bone hyperplasia. Regenerative medicine, including cell therapy, could be one of the leading options for nasal mucosa regeneration. To date, there is a lack of effective models for evaluating treatments for prevention of bone hyperplasia that occurs after sinus surgery. The purpose of this study was to develop a model of nasal mucosal removal to evaluate cellular therapies. The model was created in rabbits, a species with a wide nasal structure, and was generated by approaching the maxillary sinus from the nasal bone side and solely removing the maxillary sinus mucosa without destroying the structures in the nasal cavity. Adipose-derived mesenchymal stromal cell sheets prepared in temperature-responsive cell culture dishes were examined for the effect of transplantation in the animal model. Intranasal evaluation was assessed by micro-computed tomography and tissue staining. Significant bone hyperplasia in the maxillary sinus occurred on the side of mucosal removal, and no bone hyperplasia occurred in the control sham side in the same rabbits on postoperative day 28. Bone hyperplasia was observed over a short time period, with the presence of bone hyperplasia in the maxillary sinus on day 14 and calcification of the bone on day 28. The adipose-derived mesenchymal stromal cell (ADSC) sheet was transplantable in a nasal mucosa-removal model. No significant differences in bone hyperplasia were found between the transplantation side and the sham side in terms of the effect of transplantation of the ADSC sheet; however, bone hyperplasia tended to be suppressed on the transplantation side. This animal model is simple, highly reproducible, and does not require special equipment or drugs. In addition, this model can be used for various therapeutic interventions, including cell therapy. The presence or absence of the nasal mucosa affects bone remodeling, which highlights the importance of regeneration of the nasal mucosa. In the nasal mucosal regeneration therapy, the ADSC sheet had an inhibitory effect on bone hyperplasia. The nasal mucosa-removal model allows observation of conditions associated with nasal mucosa removal and evaluation of the effectiveness of cell therapy.

Identifiants

pubmed: 33490320
doi: 10.1016/j.reth.2020.12.004
pii: S2352-3204(20)30100-0
pmc: PMC7797364
doi:

Types de publication

Journal Article

Langues

eng

Pagination

32-41

Informations de copyright

© 2021 The Japanese Society for Regenerative Medicine. Production and hosting by Elsevier B.V.

Déclaration de conflit d'intérêts

Co-author Masayuki Yamato is an equity holder of CellSeed Inc.; Tokyo Women's Medical University currently receives research funding from CellSeed, Inc. Dr. M. Yamato is also an advisor of commercial efforts, Helios, and NIPPI (Japan).

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Auteurs

Shun Kikuchi (S)

Institute of Advanced Biomedical Engineering and Science, Tokyo Women's Medical University, Tokyo, Japan.
Department of Otorhinolaryngology, Jikei University School of Medicine, Tokyo, Japan.

Tsunetaro Morino (T)

Institute of Advanced Biomedical Engineering and Science, Tokyo Women's Medical University, Tokyo, Japan.
Department of Otorhinolaryngology, Jikei University School of Medicine, Tokyo, Japan.

Ryo Takagi (R)

Institute of Advanced Biomedical Engineering and Science, Tokyo Women's Medical University, Tokyo, Japan.

Otori Nobuyoshi (O)

Department of Otorhinolaryngology, Jikei University School of Medicine, Tokyo, Japan.

Hiromi Kojima (H)

Department of Otorhinolaryngology, Jikei University School of Medicine, Tokyo, Japan.

Masayuki Yamato (M)

Institute of Advanced Biomedical Engineering and Science, Tokyo Women's Medical University, Tokyo, Japan.

Classifications MeSH