Cargando…
Effect of cryopreservation on proliferation and differentiation of periodontal ligament stem cell sheets
BACKGROUND: Cryopreservation has been extensively applied to the long-term storage of a diverse range of biological materials. However, no comprehensive study is currently available on the cryopreservation of periodontal ligament stem cell (PDLSC) sheets which have been suggested as excellent transp...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5392927/ https://www.ncbi.nlm.nih.gov/pubmed/28412975 http://dx.doi.org/10.1186/s13287-017-0530-5 |
_version_ | 1783229492504821760 |
---|---|
author | Li, Mengying Feng, Cheng Gu, Xiuge He, Qin Wei, Fulan |
author_facet | Li, Mengying Feng, Cheng Gu, Xiuge He, Qin Wei, Fulan |
author_sort | Li, Mengying |
collection | PubMed |
description | BACKGROUND: Cryopreservation has been extensively applied to the long-term storage of a diverse range of biological materials. However, no comprehensive study is currently available on the cryopreservation of periodontal ligament stem cell (PDLSC) sheets which have been suggested as excellent transplant materials for periodontal tissue regeneration. The aim of this study is to investigate the effect of cryopreservation on the structural integrity and functional viability of PDLSC sheets. METHODS: PDLSC sheets prepared from extracted human molars were divided into two groups: the cryopreservation group (cPDLSC sheets) and the freshly prepared control group (fPDLSC sheets). The cPDLSC sheets were cryopreserved in a solution consisting of 90% fetal bovine serum and 10% dimethyl sulfoxide for 3 months. Cell viability and cell proliferation rates of PDLSCs in both groups were evaluated by cell viability assay and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, respectively. The multilineage differentiation potentials of the cells were assessed by von Kossa staining and Oil Red O staining. The chromosomal stability was examined by karyotype analysis. Moreover, the cell sheets in each group were transplanted subcutaneously into the dorsal site of nude mice, after which Sirius Red staining was performed to analyze the efficiency of tissue regeneration. RESULTS: The PDLSCs derived from both groups of cell sheets showed no significant difference in their viability, proliferative capacities, and multilineage differentiation potentials, as well as chromosomal stability. Furthermore, transplantation experiments based on a mouse model demonstrated that the cPDLSC sheets were equally effective in generating viable osteoid tissues in vivo as their freshly prepared counterparts. In both cases, the regenerated tissues showed similar network patterns of bone-like matrix. CONCLUSIONS: Our results offer convincing evidence that cryopreservation does not alter the biological properties of PDLSC sheets and could enhance their clinical utility in tissue regeneration. |
format | Online Article Text |
id | pubmed-5392927 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53929272017-04-20 Effect of cryopreservation on proliferation and differentiation of periodontal ligament stem cell sheets Li, Mengying Feng, Cheng Gu, Xiuge He, Qin Wei, Fulan Stem Cell Res Ther Research BACKGROUND: Cryopreservation has been extensively applied to the long-term storage of a diverse range of biological materials. However, no comprehensive study is currently available on the cryopreservation of periodontal ligament stem cell (PDLSC) sheets which have been suggested as excellent transplant materials for periodontal tissue regeneration. The aim of this study is to investigate the effect of cryopreservation on the structural integrity and functional viability of PDLSC sheets. METHODS: PDLSC sheets prepared from extracted human molars were divided into two groups: the cryopreservation group (cPDLSC sheets) and the freshly prepared control group (fPDLSC sheets). The cPDLSC sheets were cryopreserved in a solution consisting of 90% fetal bovine serum and 10% dimethyl sulfoxide for 3 months. Cell viability and cell proliferation rates of PDLSCs in both groups were evaluated by cell viability assay and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, respectively. The multilineage differentiation potentials of the cells were assessed by von Kossa staining and Oil Red O staining. The chromosomal stability was examined by karyotype analysis. Moreover, the cell sheets in each group were transplanted subcutaneously into the dorsal site of nude mice, after which Sirius Red staining was performed to analyze the efficiency of tissue regeneration. RESULTS: The PDLSCs derived from both groups of cell sheets showed no significant difference in their viability, proliferative capacities, and multilineage differentiation potentials, as well as chromosomal stability. Furthermore, transplantation experiments based on a mouse model demonstrated that the cPDLSC sheets were equally effective in generating viable osteoid tissues in vivo as their freshly prepared counterparts. In both cases, the regenerated tissues showed similar network patterns of bone-like matrix. CONCLUSIONS: Our results offer convincing evidence that cryopreservation does not alter the biological properties of PDLSC sheets and could enhance their clinical utility in tissue regeneration. BioMed Central 2017-04-17 /pmc/articles/PMC5392927/ /pubmed/28412975 http://dx.doi.org/10.1186/s13287-017-0530-5 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Li, Mengying Feng, Cheng Gu, Xiuge He, Qin Wei, Fulan Effect of cryopreservation on proliferation and differentiation of periodontal ligament stem cell sheets |
title | Effect of cryopreservation on proliferation and differentiation of periodontal ligament stem cell sheets |
title_full | Effect of cryopreservation on proliferation and differentiation of periodontal ligament stem cell sheets |
title_fullStr | Effect of cryopreservation on proliferation and differentiation of periodontal ligament stem cell sheets |
title_full_unstemmed | Effect of cryopreservation on proliferation and differentiation of periodontal ligament stem cell sheets |
title_short | Effect of cryopreservation on proliferation and differentiation of periodontal ligament stem cell sheets |
title_sort | effect of cryopreservation on proliferation and differentiation of periodontal ligament stem cell sheets |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5392927/ https://www.ncbi.nlm.nih.gov/pubmed/28412975 http://dx.doi.org/10.1186/s13287-017-0530-5 |
work_keys_str_mv | AT limengying effectofcryopreservationonproliferationanddifferentiationofperiodontalligamentstemcellsheets AT fengcheng effectofcryopreservationonproliferationanddifferentiationofperiodontalligamentstemcellsheets AT guxiuge effectofcryopreservationonproliferationanddifferentiationofperiodontalligamentstemcellsheets AT heqin effectofcryopreservationonproliferationanddifferentiationofperiodontalligamentstemcellsheets AT weifulan effectofcryopreservationonproliferationanddifferentiationofperiodontalligamentstemcellsheets |