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Comparative gene expression analysis of stemness between periodontal ligament and umbilical cord tissues in humans

BACKGROUND/PURPOSE: Due to their regenerative potential, periodontal ligament (PDL) and umbilical cord (UBC) tissues are an attractive potential mesenchymal stem cells (MSCs) source. This study compared the expression patterns of genes related to stemness between fresh PDL and UBC tissues. MATERIALS...

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Autores principales: Lee, Hyung-Joo, Jeon, Mijeong, Kim, Young-Han, Kim, Seong-Oh, Lee, Ko Eun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Association for Dental Sciences of the Republic of China 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9831792/
https://www.ncbi.nlm.nih.gov/pubmed/36643271
http://dx.doi.org/10.1016/j.jds.2022.06.005
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author Lee, Hyung-Joo
Jeon, Mijeong
Kim, Young-Han
Kim, Seong-Oh
Lee, Ko Eun
author_facet Lee, Hyung-Joo
Jeon, Mijeong
Kim, Young-Han
Kim, Seong-Oh
Lee, Ko Eun
author_sort Lee, Hyung-Joo
collection PubMed
description BACKGROUND/PURPOSE: Due to their regenerative potential, periodontal ligament (PDL) and umbilical cord (UBC) tissues are an attractive potential mesenchymal stem cells (MSCs) source. This study compared the expression patterns of genes related to stemness between fresh PDL and UBC tissues. MATERIALS AND METHODS: PDL tissues were collected from 38 permanent premolars extracted for orthodontic purposes, and UBC tissues were obtained from three newborns. Each sample was immediately frozen to prevent RNA degradation. cDNA microarray analysis, quantitative real-time polymerase chain reaction (PCR), and immunohistochemical staining were performed. Gene expression patterns associated with dental stemness (DS) and induced pluripotent stemness (iPS) were compared between PDL and UBC tissues. RESULTS: In the cDNA microarray analyses, the expressions of most iPS genes were greater in the PDL than in the UBC. Meanwhile, the expressions of most DS genes were greater in the UBC than in the PDL. Quantitative real-time PCR analyses showed that the expression levels of matrix metallopeptidase 13 (MMP13), ADAM metallopeptidase domain 22 (ADAM22), vascular cell adhesion protein 1 (VCAM1), and kruppel-like factor 4 (KLF4) genes were greater in the PDL than in the UBC, while the expressions of melanoma cell adhesion molecule (MCAM) and activated leukocyte cell adhesion molecule (ALCAM) were greater in the UBC than in the PDL. CONCLUSION: These results suggest that UBC and PDL tissues showed slightly different expression patterns of genes related to stemness, which warrants further investigation to use these tissues for future regeneration and implantation therapies.
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spelling pubmed-98317922023-01-13 Comparative gene expression analysis of stemness between periodontal ligament and umbilical cord tissues in humans Lee, Hyung-Joo Jeon, Mijeong Kim, Young-Han Kim, Seong-Oh Lee, Ko Eun J Dent Sci Original Article BACKGROUND/PURPOSE: Due to their regenerative potential, periodontal ligament (PDL) and umbilical cord (UBC) tissues are an attractive potential mesenchymal stem cells (MSCs) source. This study compared the expression patterns of genes related to stemness between fresh PDL and UBC tissues. MATERIALS AND METHODS: PDL tissues were collected from 38 permanent premolars extracted for orthodontic purposes, and UBC tissues were obtained from three newborns. Each sample was immediately frozen to prevent RNA degradation. cDNA microarray analysis, quantitative real-time polymerase chain reaction (PCR), and immunohistochemical staining were performed. Gene expression patterns associated with dental stemness (DS) and induced pluripotent stemness (iPS) were compared between PDL and UBC tissues. RESULTS: In the cDNA microarray analyses, the expressions of most iPS genes were greater in the PDL than in the UBC. Meanwhile, the expressions of most DS genes were greater in the UBC than in the PDL. Quantitative real-time PCR analyses showed that the expression levels of matrix metallopeptidase 13 (MMP13), ADAM metallopeptidase domain 22 (ADAM22), vascular cell adhesion protein 1 (VCAM1), and kruppel-like factor 4 (KLF4) genes were greater in the PDL than in the UBC, while the expressions of melanoma cell adhesion molecule (MCAM) and activated leukocyte cell adhesion molecule (ALCAM) were greater in the UBC than in the PDL. CONCLUSION: These results suggest that UBC and PDL tissues showed slightly different expression patterns of genes related to stemness, which warrants further investigation to use these tissues for future regeneration and implantation therapies. Association for Dental Sciences of the Republic of China 2023-01 2022-06-29 /pmc/articles/PMC9831792/ /pubmed/36643271 http://dx.doi.org/10.1016/j.jds.2022.06.005 Text en © 2022 Association for Dental Sciences of the Republic of China. Publishing services by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Lee, Hyung-Joo
Jeon, Mijeong
Kim, Young-Han
Kim, Seong-Oh
Lee, Ko Eun
Comparative gene expression analysis of stemness between periodontal ligament and umbilical cord tissues in humans
title Comparative gene expression analysis of stemness between periodontal ligament and umbilical cord tissues in humans
title_full Comparative gene expression analysis of stemness between periodontal ligament and umbilical cord tissues in humans
title_fullStr Comparative gene expression analysis of stemness between periodontal ligament and umbilical cord tissues in humans
title_full_unstemmed Comparative gene expression analysis of stemness between periodontal ligament and umbilical cord tissues in humans
title_short Comparative gene expression analysis of stemness between periodontal ligament and umbilical cord tissues in humans
title_sort comparative gene expression analysis of stemness between periodontal ligament and umbilical cord tissues in humans
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9831792/
https://www.ncbi.nlm.nih.gov/pubmed/36643271
http://dx.doi.org/10.1016/j.jds.2022.06.005
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