Compare features of human dental pulp cells cultured from pulp tissues with and without cryopreservation

Background and Aims. Teeth extracted are usually disposed as bio-waste whereas they could serve as an autologous tissue for culturing multipotent dental pulp cells which have application potential in regenerative medicine. This study aimed to examine the feasibility of cryopreserving dental pulp tis...

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Autores principales: Ming Yan, Ola A. Nada, Ralf Smeets, Martin Gosau, Reinhard E. Friedrich, Lan Kluwe
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Publicado: Palacký University Olomouc, Faculty of Medicine and Dentistry 2021
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Acceso en línea:https://doaj.org/article/7745f9ddf8884cb9a5e59605657b1408
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spelling oai:doaj.org-article:7745f9ddf8884cb9a5e59605657b14082021-11-29T09:17:21ZCompare features of human dental pulp cells cultured from pulp tissues with and without cryopreservation1213-81181804-7521https://doaj.org/article/7745f9ddf8884cb9a5e59605657b14082021-11-01T00:00:00Zhttps://biomed.papers.upol.cz/artkey/bio-202104-0015_compare-features-of-human-dental-pulp-cells-cultured-from-pulp-tissues-with-and-without-cryopreservation.phphttps://doaj.org/toc/1213-8118https://doaj.org/toc/1804-7521Background and Aims. Teeth extracted are usually disposed as bio-waste whereas they could serve as an autologous tissue for culturing multipotent dental pulp cells which have application potential in regenerative medicine. This study aimed to examine the feasibility of cryopreserving dental pulp tissue at teeth extraction for later culturing of cells. Methods. The pulp tissue from each of a total of 10 teeth was cut into small fragments which were then divided into two portions. One portion was directly used for culturing pulp cells using the explant method. The other portion was cryopreserved with 10% DMSO in liquid nitrogen for at least one month and then thawed for culturing pulp cells. Results. Vital cells were obtained from all the 10 pulp fragment suspensions which went through cryopreservation. The cell outgrowth from the explants of cryopreserved pulp fragments was two days later than that of corresponding fresh pulp tissue. Otherwise, no difference was observed in proliferation, expression of stem cell markers and differentiation into adipose cells and osteoblasts between the two groups of cells cultured from the fresh or the cryopreserved pulp fragments. Conclusions. Cryopreserving fragmented dental pulp tissue provides a feasible option for saving pulp tissues as autologous cell sources for possible later application.Ming YanOla A. NadaRalf SmeetsMartin GosauReinhard E. FriedrichLan KluwePalacký University Olomouc, Faculty of Medicine and Dentistryarticledental pulp cellsdifferentiationdental pulp tissuecell culturetissue cryopreservationosteogenic differentiationadipogenic differentiationMedicineRENBiomedical Papers, Vol 165, Iss 4, Pp 445-451 (2021)
institution DOAJ
collection DOAJ
language EN
topic dental pulp cells
differentiation
dental pulp tissue
cell culture
tissue cryopreservation
osteogenic differentiation
adipogenic differentiation
Medicine
R
spellingShingle dental pulp cells
differentiation
dental pulp tissue
cell culture
tissue cryopreservation
osteogenic differentiation
adipogenic differentiation
Medicine
R
Ming Yan
Ola A. Nada
Ralf Smeets
Martin Gosau
Reinhard E. Friedrich
Lan Kluwe
Compare features of human dental pulp cells cultured from pulp tissues with and without cryopreservation
description Background and Aims. Teeth extracted are usually disposed as bio-waste whereas they could serve as an autologous tissue for culturing multipotent dental pulp cells which have application potential in regenerative medicine. This study aimed to examine the feasibility of cryopreserving dental pulp tissue at teeth extraction for later culturing of cells. Methods. The pulp tissue from each of a total of 10 teeth was cut into small fragments which were then divided into two portions. One portion was directly used for culturing pulp cells using the explant method. The other portion was cryopreserved with 10% DMSO in liquid nitrogen for at least one month and then thawed for culturing pulp cells. Results. Vital cells were obtained from all the 10 pulp fragment suspensions which went through cryopreservation. The cell outgrowth from the explants of cryopreserved pulp fragments was two days later than that of corresponding fresh pulp tissue. Otherwise, no difference was observed in proliferation, expression of stem cell markers and differentiation into adipose cells and osteoblasts between the two groups of cells cultured from the fresh or the cryopreserved pulp fragments. Conclusions. Cryopreserving fragmented dental pulp tissue provides a feasible option for saving pulp tissues as autologous cell sources for possible later application.
format article
author Ming Yan
Ola A. Nada
Ralf Smeets
Martin Gosau
Reinhard E. Friedrich
Lan Kluwe
author_facet Ming Yan
Ola A. Nada
Ralf Smeets
Martin Gosau
Reinhard E. Friedrich
Lan Kluwe
author_sort Ming Yan
title Compare features of human dental pulp cells cultured from pulp tissues with and without cryopreservation
title_short Compare features of human dental pulp cells cultured from pulp tissues with and without cryopreservation
title_full Compare features of human dental pulp cells cultured from pulp tissues with and without cryopreservation
title_fullStr Compare features of human dental pulp cells cultured from pulp tissues with and without cryopreservation
title_full_unstemmed Compare features of human dental pulp cells cultured from pulp tissues with and without cryopreservation
title_sort compare features of human dental pulp cells cultured from pulp tissues with and without cryopreservation
publisher Palacký University Olomouc, Faculty of Medicine and Dentistry
publishDate 2021
url https://doaj.org/article/7745f9ddf8884cb9a5e59605657b1408
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AT martingosau comparefeaturesofhumandentalpulpcellsculturedfrompulptissueswithandwithoutcryopreservation
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