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Evaluation of Acellular Dermal Matrix (ADM) as a Scaffold for Adipose-Derived Stem Cell Transfer in the Rat Model

BACKGROUND: This study was designed for the evaluation of Acellular Dermal Matrix (ADM) as a scaffold for adipose-derived stem cell transferring in the rat model. METHODS: This experimental study was done in the Burn Research Center of Iran University of Medical Sciences and Bonyakhteh Research Cent...

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Autores principales: Jahanian, Maryam, Hoseini, Sara, Atashi, Amir, Saberi, Mohsen, Hoseini, Seyyed Aboozar, Mozaffari, Kambiz, Fatemi, Mohammad Javad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iranian Society for Plastic Surgeons 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8290445/
https://www.ncbi.nlm.nih.gov/pubmed/34307100
http://dx.doi.org/10.29252/wjps.10.2.67
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author Jahanian, Maryam
Hoseini, Sara
Atashi, Amir
Saberi, Mohsen
Hoseini, Seyyed Aboozar
Mozaffari, Kambiz
Fatemi, Mohammad Javad
author_facet Jahanian, Maryam
Hoseini, Sara
Atashi, Amir
Saberi, Mohsen
Hoseini, Seyyed Aboozar
Mozaffari, Kambiz
Fatemi, Mohammad Javad
author_sort Jahanian, Maryam
collection PubMed
description BACKGROUND: This study was designed for the evaluation of Acellular Dermal Matrix (ADM) as a scaffold for adipose-derived stem cell transferring in the rat model. METHODS: This experimental study was done in the Burn Research Center of Iran University of Medical Sciences and Bonyakhteh Research Center, Tehran, Iran according to the standards of laboratory animals. Overall, 26 healthy Sprague-Dawley rats were used. Two of them were used to prepare ADM. In group one, the first wound on each, rat was spread with the mixture of fibrin gel and autologous stem cell. Only the stem cells combined with fibrinogen were spread on the other wound. In group two, the first wound on each rat was covered only with ADM, and the second wound was covered with gauze Vaseline. To perform sampling we used observation and photography at 7-30 days. Overall, 48 samples were taken of all the rats using skin punch biopsy on the 30th day for histopathology evaluation. RESULTS: There were significant differences in each group; however, the difference between different groups on days was not significant. In pathology, epithelialization, vascularization, the amount of collagen, collagen arrangement, the number of fibroblasts, and inflammation indices were investigated. The total score in each group was used for analysis. In statistical analysis, there was no pathology score difference among groups. CONCLUSION: Using stem cells with or without ADM could not enhance the process of wound healing or improve pathology indices.
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spelling pubmed-82904452021-07-22 Evaluation of Acellular Dermal Matrix (ADM) as a Scaffold for Adipose-Derived Stem Cell Transfer in the Rat Model Jahanian, Maryam Hoseini, Sara Atashi, Amir Saberi, Mohsen Hoseini, Seyyed Aboozar Mozaffari, Kambiz Fatemi, Mohammad Javad World J Plast Surg Original Article BACKGROUND: This study was designed for the evaluation of Acellular Dermal Matrix (ADM) as a scaffold for adipose-derived stem cell transferring in the rat model. METHODS: This experimental study was done in the Burn Research Center of Iran University of Medical Sciences and Bonyakhteh Research Center, Tehran, Iran according to the standards of laboratory animals. Overall, 26 healthy Sprague-Dawley rats were used. Two of them were used to prepare ADM. In group one, the first wound on each, rat was spread with the mixture of fibrin gel and autologous stem cell. Only the stem cells combined with fibrinogen were spread on the other wound. In group two, the first wound on each rat was covered only with ADM, and the second wound was covered with gauze Vaseline. To perform sampling we used observation and photography at 7-30 days. Overall, 48 samples were taken of all the rats using skin punch biopsy on the 30th day for histopathology evaluation. RESULTS: There were significant differences in each group; however, the difference between different groups on days was not significant. In pathology, epithelialization, vascularization, the amount of collagen, collagen arrangement, the number of fibroblasts, and inflammation indices were investigated. The total score in each group was used for analysis. In statistical analysis, there was no pathology score difference among groups. CONCLUSION: Using stem cells with or without ADM could not enhance the process of wound healing or improve pathology indices. Iranian Society for Plastic Surgeons 2021-05 /pmc/articles/PMC8290445/ /pubmed/34307100 http://dx.doi.org/10.29252/wjps.10.2.67 Text en https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Jahanian, Maryam
Hoseini, Sara
Atashi, Amir
Saberi, Mohsen
Hoseini, Seyyed Aboozar
Mozaffari, Kambiz
Fatemi, Mohammad Javad
Evaluation of Acellular Dermal Matrix (ADM) as a Scaffold for Adipose-Derived Stem Cell Transfer in the Rat Model
title Evaluation of Acellular Dermal Matrix (ADM) as a Scaffold for Adipose-Derived Stem Cell Transfer in the Rat Model
title_full Evaluation of Acellular Dermal Matrix (ADM) as a Scaffold for Adipose-Derived Stem Cell Transfer in the Rat Model
title_fullStr Evaluation of Acellular Dermal Matrix (ADM) as a Scaffold for Adipose-Derived Stem Cell Transfer in the Rat Model
title_full_unstemmed Evaluation of Acellular Dermal Matrix (ADM) as a Scaffold for Adipose-Derived Stem Cell Transfer in the Rat Model
title_short Evaluation of Acellular Dermal Matrix (ADM) as a Scaffold for Adipose-Derived Stem Cell Transfer in the Rat Model
title_sort evaluation of acellular dermal matrix (adm) as a scaffold for adipose-derived stem cell transfer in the rat model
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8290445/
https://www.ncbi.nlm.nih.gov/pubmed/34307100
http://dx.doi.org/10.29252/wjps.10.2.67
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