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Analysis of side population cells derived from dental pulp tissue

Kenmotsu M, Matsuzaka K, Kokubu E, Azuma T, Inoue T. Analysis of side population cells derived from dental pulp tissue. International Endodontic Journal. AIM: To investigate the characteristics of side population (SP) cells derived from the dental pulp of young and aged rats. METHODOLOGY: Maxillary...

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Detalles Bibliográficos
Autores principales: Kenmotsu, M, Matsuzaka, K, Kokubu, E, Azuma, T, Inoue, T
Formato: Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3033520/
https://www.ncbi.nlm.nih.gov/pubmed/21029119
http://dx.doi.org/10.1111/j.1365-2591.2010.01789.x
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author Kenmotsu, M
Matsuzaka, K
Kokubu, E
Azuma, T
Inoue, T
author_facet Kenmotsu, M
Matsuzaka, K
Kokubu, E
Azuma, T
Inoue, T
author_sort Kenmotsu, M
collection PubMed
description Kenmotsu M, Matsuzaka K, Kokubu E, Azuma T, Inoue T. Analysis of side population cells derived from dental pulp tissue. International Endodontic Journal. AIM: To investigate the characteristics of side population (SP) cells derived from the dental pulp of young and aged rats. METHODOLOGY: Maxillary and mandibular incisors were extracted from 5-week-old (young) rats and 60- to 80-week-old (aged) rats. Coronal pulp tissue was removed mechanically, and single-cell suspensions were prepared using collagenase and dispase. Cells were stained with Hoechst 33342 and sorted with an fluorescence-activated cell sorter (FACS). Isolated SP and main population (MP) cells were analysed by real-time reverse transcription polymerase chain reaction, immunohistochemical localization and cell cycle determination. Two-way analysis of variance and the multiple comparison Scheffè test were used for statistical analysis (P < 0.05). RESULTS: Approximately 0.40% of pulp cells in young rats and 0.11% in aged rats comprised SP cells. SP cells expressed a higher mRNA level of ATP-binding cassette transporter G2 (ABCG2), but lower mRNA levels of nestin, alkaline phosphatase, p16 and p57 than MP cells in both age groups. Immunohistochemical observation revealed ABCG2-positive cells localized in the cell-rich zone and nestin in the odontoblastic layer in both groups. Furthermore, the majority of both young and aged SP and MP cells were in growth arrest of the G(0)/G(1) phase. CONCLUSION: The FACS analysis revealed a decrease in the proportion of SP cells with age, whilst p16 mRNA expression indicated an increase in cell senescence. The cell cycles of SP and MP cells from both young and aged dental pulp were generally in the G0/G1 phase.
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spelling pubmed-30335202011-02-15 Analysis of side population cells derived from dental pulp tissue Kenmotsu, M Matsuzaka, K Kokubu, E Azuma, T Inoue, T Int Endod J Original Scientific Articles Kenmotsu M, Matsuzaka K, Kokubu E, Azuma T, Inoue T. Analysis of side population cells derived from dental pulp tissue. International Endodontic Journal. AIM: To investigate the characteristics of side population (SP) cells derived from the dental pulp of young and aged rats. METHODOLOGY: Maxillary and mandibular incisors were extracted from 5-week-old (young) rats and 60- to 80-week-old (aged) rats. Coronal pulp tissue was removed mechanically, and single-cell suspensions were prepared using collagenase and dispase. Cells were stained with Hoechst 33342 and sorted with an fluorescence-activated cell sorter (FACS). Isolated SP and main population (MP) cells were analysed by real-time reverse transcription polymerase chain reaction, immunohistochemical localization and cell cycle determination. Two-way analysis of variance and the multiple comparison Scheffè test were used for statistical analysis (P < 0.05). RESULTS: Approximately 0.40% of pulp cells in young rats and 0.11% in aged rats comprised SP cells. SP cells expressed a higher mRNA level of ATP-binding cassette transporter G2 (ABCG2), but lower mRNA levels of nestin, alkaline phosphatase, p16 and p57 than MP cells in both age groups. Immunohistochemical observation revealed ABCG2-positive cells localized in the cell-rich zone and nestin in the odontoblastic layer in both groups. Furthermore, the majority of both young and aged SP and MP cells were in growth arrest of the G(0)/G(1) phase. CONCLUSION: The FACS analysis revealed a decrease in the proportion of SP cells with age, whilst p16 mRNA expression indicated an increase in cell senescence. The cell cycles of SP and MP cells from both young and aged dental pulp were generally in the G0/G1 phase. Blackwell Publishing Ltd 2010-12 /pmc/articles/PMC3033520/ /pubmed/21029119 http://dx.doi.org/10.1111/j.1365-2591.2010.01789.x Text en Copyright © 2010 International Endodontic Journal http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Original Scientific Articles
Kenmotsu, M
Matsuzaka, K
Kokubu, E
Azuma, T
Inoue, T
Analysis of side population cells derived from dental pulp tissue
title Analysis of side population cells derived from dental pulp tissue
title_full Analysis of side population cells derived from dental pulp tissue
title_fullStr Analysis of side population cells derived from dental pulp tissue
title_full_unstemmed Analysis of side population cells derived from dental pulp tissue
title_short Analysis of side population cells derived from dental pulp tissue
title_sort analysis of side population cells derived from dental pulp tissue
topic Original Scientific Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3033520/
https://www.ncbi.nlm.nih.gov/pubmed/21029119
http://dx.doi.org/10.1111/j.1365-2591.2010.01789.x
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