Cargando…
Autologous nasal chondrocytes delivered by injectable hydrogel for in vivo articular cartilage regeneration
Cell based tissue engineering serves as a promising strategy for articular cartilage repair, which remains a challenge both for researchers and clinicians. The aim of this research was to assess the potential of autologous nasal chondrocytes (NCs) combined with alginate hydrogel as injectable constr...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5829115/ https://www.ncbi.nlm.nih.gov/pubmed/28815373 http://dx.doi.org/10.1007/s10561-017-9649-y |
_version_ | 1783302739726434304 |
---|---|
author | Chen, Wenliang Li, Changhua Peng, Maoxiu Xie, Bingju Zhang, Lei Tang, Xiaojun |
author_facet | Chen, Wenliang Li, Changhua Peng, Maoxiu Xie, Bingju Zhang, Lei Tang, Xiaojun |
author_sort | Chen, Wenliang |
collection | PubMed |
description | Cell based tissue engineering serves as a promising strategy for articular cartilage repair, which remains a challenge both for researchers and clinicians. The aim of this research was to assess the potential of autologous nasal chondrocytes (NCs) combined with alginate hydrogel as injectable constructs for rabbit articular cartilage repair. Autologous nasal chondrocytes were isolated from rabbit nasal septum, expanded either on monolayer or in 3D alginate hydrogel. In vitro, DNA quantification revealed that NCs can proliferate stable in 3D alginate matrix, but slower than that cultured in monolayer. Further, a higher synthesis rate of glycosaminoglycans (GAGs) was detected by GAG measurement in 3D alginate culture. Gene expression analysis at different time point (day 1, 7, 14) showed that 3D culture of NCs in alginate up-regulated chondrogenic markers (Col2A1, ACAN SOX9), meanwhile down-regulated dedifferentiation related gene (Col1A1). In vivo, autologous nasal chondrocytes combined with alginate hydrogel were used for repairing rabbit knee osteochondral defect (Alg + NC group). Histological staining indicated that Alg + NC group obtained superior and more hyaline-like repaired tissue both at 3 and 6 months after surgery. Mechanical analysis showed that the repaired tissue in the Alg + NC group possessed similar mechanical properties to the native cartilage. In conclusion, nasal chondrocytes appeared to be a very promising seed cell source for cartilage tissue engineering, and alginate hydrogel can serve as suitable delivery system. |
format | Online Article Text |
id | pubmed-5829115 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-58291152018-03-01 Autologous nasal chondrocytes delivered by injectable hydrogel for in vivo articular cartilage regeneration Chen, Wenliang Li, Changhua Peng, Maoxiu Xie, Bingju Zhang, Lei Tang, Xiaojun Cell Tissue Bank Article Cell based tissue engineering serves as a promising strategy for articular cartilage repair, which remains a challenge both for researchers and clinicians. The aim of this research was to assess the potential of autologous nasal chondrocytes (NCs) combined with alginate hydrogel as injectable constructs for rabbit articular cartilage repair. Autologous nasal chondrocytes were isolated from rabbit nasal septum, expanded either on monolayer or in 3D alginate hydrogel. In vitro, DNA quantification revealed that NCs can proliferate stable in 3D alginate matrix, but slower than that cultured in monolayer. Further, a higher synthesis rate of glycosaminoglycans (GAGs) was detected by GAG measurement in 3D alginate culture. Gene expression analysis at different time point (day 1, 7, 14) showed that 3D culture of NCs in alginate up-regulated chondrogenic markers (Col2A1, ACAN SOX9), meanwhile down-regulated dedifferentiation related gene (Col1A1). In vivo, autologous nasal chondrocytes combined with alginate hydrogel were used for repairing rabbit knee osteochondral defect (Alg + NC group). Histological staining indicated that Alg + NC group obtained superior and more hyaline-like repaired tissue both at 3 and 6 months after surgery. Mechanical analysis showed that the repaired tissue in the Alg + NC group possessed similar mechanical properties to the native cartilage. In conclusion, nasal chondrocytes appeared to be a very promising seed cell source for cartilage tissue engineering, and alginate hydrogel can serve as suitable delivery system. Springer Netherlands 2017-08-16 2018 /pmc/articles/PMC5829115/ /pubmed/28815373 http://dx.doi.org/10.1007/s10561-017-9649-y Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Article Chen, Wenliang Li, Changhua Peng, Maoxiu Xie, Bingju Zhang, Lei Tang, Xiaojun Autologous nasal chondrocytes delivered by injectable hydrogel for in vivo articular cartilage regeneration |
title | Autologous nasal chondrocytes delivered by injectable hydrogel for in vivo articular cartilage regeneration |
title_full | Autologous nasal chondrocytes delivered by injectable hydrogel for in vivo articular cartilage regeneration |
title_fullStr | Autologous nasal chondrocytes delivered by injectable hydrogel for in vivo articular cartilage regeneration |
title_full_unstemmed | Autologous nasal chondrocytes delivered by injectable hydrogel for in vivo articular cartilage regeneration |
title_short | Autologous nasal chondrocytes delivered by injectable hydrogel for in vivo articular cartilage regeneration |
title_sort | autologous nasal chondrocytes delivered by injectable hydrogel for in vivo articular cartilage regeneration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5829115/ https://www.ncbi.nlm.nih.gov/pubmed/28815373 http://dx.doi.org/10.1007/s10561-017-9649-y |
work_keys_str_mv | AT chenwenliang autologousnasalchondrocytesdeliveredbyinjectablehydrogelforinvivoarticularcartilageregeneration AT lichanghua autologousnasalchondrocytesdeliveredbyinjectablehydrogelforinvivoarticularcartilageregeneration AT pengmaoxiu autologousnasalchondrocytesdeliveredbyinjectablehydrogelforinvivoarticularcartilageregeneration AT xiebingju autologousnasalchondrocytesdeliveredbyinjectablehydrogelforinvivoarticularcartilageregeneration AT zhanglei autologousnasalchondrocytesdeliveredbyinjectablehydrogelforinvivoarticularcartilageregeneration AT tangxiaojun autologousnasalchondrocytesdeliveredbyinjectablehydrogelforinvivoarticularcartilageregeneration |