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TGF-β1 and CD68 immunoexpression in capsules formed by textured implants with and without mesh coverage: a study on female rats

PURPOSE: To evaluate fibrosis formation and number of macrophages in capsules formed around textured implants without and with mesh coverage. METHODS: Fibrosis was analyzed through transforming growth factor-beta 1 (TGF-β1) immunomarker expression and the number of macrophages through CD68 percentag...

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Autores principales: Berger, Ralf, Ribas, Jurandir Marcondes, de Souza, Marcelo Augusto, de Paula, Pedro Henrique, Doubek, João Gabriel Cavazzani, Pires, Rafael de Castro e Souza, Nassif, Paulo Afonso Nunes, Silva, Eduardo Nascimento
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9020789/
https://www.ncbi.nlm.nih.gov/pubmed/35475808
http://dx.doi.org/10.1590/acb370201
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author Berger, Ralf
Ribas, Jurandir Marcondes
de Souza, Marcelo Augusto
de Paula, Pedro Henrique
Doubek, João Gabriel Cavazzani
Pires, Rafael de Castro e Souza
Nassif, Paulo Afonso Nunes
Silva, Eduardo Nascimento
author_facet Berger, Ralf
Ribas, Jurandir Marcondes
de Souza, Marcelo Augusto
de Paula, Pedro Henrique
Doubek, João Gabriel Cavazzani
Pires, Rafael de Castro e Souza
Nassif, Paulo Afonso Nunes
Silva, Eduardo Nascimento
author_sort Berger, Ralf
collection PubMed
description PURPOSE: To evaluate fibrosis formation and number of macrophages in capsules formed around textured implants without and with mesh coverage. METHODS: Fibrosis was analyzed through transforming growth factor-beta 1 (TGF-β1) immunomarker expression and the number of macrophages through CD68 percentage of cells in magnified field. Sixty female Wistar rats were distributed into two groups of 30 rats (unmeshed and meshed). Each group was then subdivided into two subgroups for postoperative evaluation after 30 and 90 days. The p value was adjusted by Bonferroni lower than 0.012. RESULTS: No difference was observed in fibrosis between meshed and unmeshed groups (30 days p = 0.436; 90 days p = 0.079) and from 30 to 90 days in the unmeshed group (p = 0.426). The meshed group showed higher fibrosis on the 90th day (p = 0.001). The number of macrophages was similar between groups without and with mesh coverage (30 days p = 0.218; 90 days p = 0.044), and similar between subgroups 30 and 90 days (unmeshed p = 0.085; meshed p = 0.059). CONCLUSIONS: In the meshed group, fibrosis formation was higher at 90 days and the mesh-covered implants produced capsules similar to microtextured ones when analyzing macrophages. Due to these characteristics, mesh coating did not seem to significantly affect the local fibrosis formation.
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spelling pubmed-90207892022-04-29 TGF-β1 and CD68 immunoexpression in capsules formed by textured implants with and without mesh coverage: a study on female rats Berger, Ralf Ribas, Jurandir Marcondes de Souza, Marcelo Augusto de Paula, Pedro Henrique Doubek, João Gabriel Cavazzani Pires, Rafael de Castro e Souza Nassif, Paulo Afonso Nunes Silva, Eduardo Nascimento Acta Cir Bras Original Article PURPOSE: To evaluate fibrosis formation and number of macrophages in capsules formed around textured implants without and with mesh coverage. METHODS: Fibrosis was analyzed through transforming growth factor-beta 1 (TGF-β1) immunomarker expression and the number of macrophages through CD68 percentage of cells in magnified field. Sixty female Wistar rats were distributed into two groups of 30 rats (unmeshed and meshed). Each group was then subdivided into two subgroups for postoperative evaluation after 30 and 90 days. The p value was adjusted by Bonferroni lower than 0.012. RESULTS: No difference was observed in fibrosis between meshed and unmeshed groups (30 days p = 0.436; 90 days p = 0.079) and from 30 to 90 days in the unmeshed group (p = 0.426). The meshed group showed higher fibrosis on the 90th day (p = 0.001). The number of macrophages was similar between groups without and with mesh coverage (30 days p = 0.218; 90 days p = 0.044), and similar between subgroups 30 and 90 days (unmeshed p = 0.085; meshed p = 0.059). CONCLUSIONS: In the meshed group, fibrosis formation was higher at 90 days and the mesh-covered implants produced capsules similar to microtextured ones when analyzing macrophages. Due to these characteristics, mesh coating did not seem to significantly affect the local fibrosis formation. Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia 2022-04-22 /pmc/articles/PMC9020789/ /pubmed/35475808 http://dx.doi.org/10.1590/acb370201 Text en https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Berger, Ralf
Ribas, Jurandir Marcondes
de Souza, Marcelo Augusto
de Paula, Pedro Henrique
Doubek, João Gabriel Cavazzani
Pires, Rafael de Castro e Souza
Nassif, Paulo Afonso Nunes
Silva, Eduardo Nascimento
TGF-β1 and CD68 immunoexpression in capsules formed by textured implants with and without mesh coverage: a study on female rats
title TGF-β1 and CD68 immunoexpression in capsules formed by textured implants with and without mesh coverage: a study on female rats
title_full TGF-β1 and CD68 immunoexpression in capsules formed by textured implants with and without mesh coverage: a study on female rats
title_fullStr TGF-β1 and CD68 immunoexpression in capsules formed by textured implants with and without mesh coverage: a study on female rats
title_full_unstemmed TGF-β1 and CD68 immunoexpression in capsules formed by textured implants with and without mesh coverage: a study on female rats
title_short TGF-β1 and CD68 immunoexpression in capsules formed by textured implants with and without mesh coverage: a study on female rats
title_sort tgf-β1 and cd68 immunoexpression in capsules formed by textured implants with and without mesh coverage: a study on female rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9020789/
https://www.ncbi.nlm.nih.gov/pubmed/35475808
http://dx.doi.org/10.1590/acb370201
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