Efecto de la Porphyromonas gingivalis sobre células pre-osteoblásticas MC3T3-E1
Antecedentes: La periodontitis es una enfermedad inflamatoria crónica, multifactorial, que afecta los tejidos de soporte dental, además es el resultado de la interacción de factores ambientales, bacterianos y del hospedador. Porphyromonas gingivalis es una de las bacterias más frecuentemente asociad...
- Autores:
-
Muriel Rios, Mariana
- Tipo de recurso:
- https://purl.org/coar/resource_type/c_7a1f
- Fecha de publicación:
- 2024
- Institución:
- Universidad El Bosque
- Repositorio:
- Repositorio U. El Bosque
- Idioma:
- spa
- OAI Identifier:
- oai:repositorio.unbosque.edu.co:20.500.12495/13708
- Acceso en línea:
- https://hdl.handle.net/20.500.12495/13708
- Palabra clave:
- Osteoblastos
Porphyromonas gingivalis
Viabilidad celular
Mineralización celular
Osteoblasts
Porphyromonas gingivalis
Cell viability
Cell mineralization
WU 100
- Rights
- License
- Attribution-NonCommercial-ShareAlike 4.0 International
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dc.title.none.fl_str_mv |
Efecto de la Porphyromonas gingivalis sobre células pre-osteoblásticas MC3T3-E1 |
dc.title.translated.none.fl_str_mv |
Effect of Porphyromonas gingivalis on pre-osteoblastic cells MC3T3-E1 |
title |
Efecto de la Porphyromonas gingivalis sobre células pre-osteoblásticas MC3T3-E1 |
spellingShingle |
Efecto de la Porphyromonas gingivalis sobre células pre-osteoblásticas MC3T3-E1 Osteoblastos Porphyromonas gingivalis Viabilidad celular Mineralización celular Osteoblasts Porphyromonas gingivalis Cell viability Cell mineralization WU 100 |
title_short |
Efecto de la Porphyromonas gingivalis sobre células pre-osteoblásticas MC3T3-E1 |
title_full |
Efecto de la Porphyromonas gingivalis sobre células pre-osteoblásticas MC3T3-E1 |
title_fullStr |
Efecto de la Porphyromonas gingivalis sobre células pre-osteoblásticas MC3T3-E1 |
title_full_unstemmed |
Efecto de la Porphyromonas gingivalis sobre células pre-osteoblásticas MC3T3-E1 |
title_sort |
Efecto de la Porphyromonas gingivalis sobre células pre-osteoblásticas MC3T3-E1 |
dc.creator.fl_str_mv |
Muriel Rios, Mariana |
dc.contributor.advisor.none.fl_str_mv |
Vargas Sánchez, Paula Castillo Perdomo, Diana |
dc.contributor.author.none.fl_str_mv |
Muriel Rios, Mariana |
dc.subject.none.fl_str_mv |
Osteoblastos Porphyromonas gingivalis Viabilidad celular Mineralización celular |
topic |
Osteoblastos Porphyromonas gingivalis Viabilidad celular Mineralización celular Osteoblasts Porphyromonas gingivalis Cell viability Cell mineralization WU 100 |
dc.subject.keywords.none.fl_str_mv |
Osteoblasts Porphyromonas gingivalis Cell viability Cell mineralization |
dc.subject.nlm.none.fl_str_mv |
WU 100 |
description |
Antecedentes: La periodontitis es una enfermedad inflamatoria crónica, multifactorial, que afecta los tejidos de soporte dental, además es el resultado de la interacción de factores ambientales, bacterianos y del hospedador. Porphyromonas gingivalis es una de las bacterias más frecuentemente asociada con la periodontitis, entender los cambios que suceden cuando entra en contacto con los osteoblastos puede darnos bases para comprender los mecanismos de la progresión de esta enfermedad. La literatura reporta algunos estudios mostrando el efecto de P. gingivalis sobre los tejidos blandos, pero no se encuentran datos concluyentes sobre su efecto en las células óseas. Objetivo: Evaluar el efecto de dos cepas de P. gingivalis en la diferenciación de las células pre-osteoblásticas MC3T3-E1 subclón 14. Materiales y Métodos: Cepas de P. gingivalis ATCC 33277 y W83 fueron sembradas en agar Brucella suplementado durante 4 días en condiciones anaeróbicas a 37°C, pasado el tiempo se ajustaron inóculos en medio de cultivo celular sin antibiótico a 1 x 108, a partir de estos se ajustó cada MOI. Se cultivaron las células MC3T3-E1 subclón 14 (ATCC) y se colocaron en contacto durante 12 horas con las cepas de P. gingivalis previamente descritas (Control +, MOI 50, MOI 100, MOI 150 y Control -), cumplido este periodo de tiempo se evaluó la viabilidad celular con el ensayo de resarzurina. Posteriormente se evaluó la formación de nódulos mineralizados a los 14 y 17 días mediante el ensayo de rojo de alizarina para las concentraciones (MOI 50 y MOI 100). Los datos obtenidos se analizaron mediante ANOVA y post test de Tukey con un nivel de confianza del 95%. Resultados: La viabilidad celular de las células MC3T3-E1 disminuyó significativamente (p<0,0001) ante la exposición a las cepas P. gingivalis W83 y P. gingivalis 33277 MOI 50 y MOI 100. El ensayo de rojo de alizarina para P. gingivalis 33277 a los 14 y 17 días de exposición no mostró diferencias significativas entre los grupos (p=0,8672 y p=0,6950, respectivamente). Para la cepa P. gingivalis W83 hubo una disminución estadísticamente significativa a los 14 y 17 días de evaluación (p=0,0423 y p=0,0321 respectivamente). Conclusiones: Las células MC3T3-E1 expuestas a cepas de P. gingivalis W83 y P. gingivalis 33277 tuvieron una disminución de la viabilidad celular, pero solo las expuestas a la cepa P. gingivalis W83 presentaron disminución en la formación de matriz mineralizada. |
publishDate |
2024 |
dc.date.accessioned.none.fl_str_mv |
2024-12-13T17:28:23Z |
dc.date.available.none.fl_str_mv |
2024-12-13T17:28:23Z |
dc.date.issued.none.fl_str_mv |
2024-11 |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_7a1f |
dc.type.local.spa.fl_str_mv |
Tesis/Trabajo de grado - Monografía - Pregrado |
dc.type.coar.none.fl_str_mv |
https://purl.org/coar/resource_type/c_7a1f |
dc.type.driver.none.fl_str_mv |
info:eu-repo/semantics/bachelorThesis |
dc.type.coarversion.none.fl_str_mv |
https://purl.org/coar/version/c_970fb48d4fbd8a85 |
format |
https://purl.org/coar/resource_type/c_7a1f |
dc.identifier.uri.none.fl_str_mv |
https://hdl.handle.net/20.500.12495/13708 |
dc.identifier.instname.spa.fl_str_mv |
instname:Universidad El Bosque |
dc.identifier.reponame.spa.fl_str_mv |
reponame:Repositorio Institucional Universidad El Bosque |
dc.identifier.repourl.none.fl_str_mv |
repourl:https://repositorio.unbosque.edu.co |
url |
https://hdl.handle.net/20.500.12495/13708 |
identifier_str_mv |
instname:Universidad El Bosque reponame:Repositorio Institucional Universidad El Bosque repourl:https://repositorio.unbosque.edu.co |
dc.language.iso.fl_str_mv |
spa |
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Periodontal disease immunology: 'double indemnity' in protecting the host. Periodontol 2000. 2013;62(1):163-202. doi:10.1111/prd.12005 62. Zainal Ariffin SH, Megat Abdul Wahab R, Abdul Razak M, et al. Evaluation of in vitro osteoblast and osteoclast differentiation from stem cell: a systematic review of morphological assays and staining techniques. PeerJ. 2024;12:e17790. Published 2024 Jul 25. doi:10.7717/peerj.17790 63. Hayashi JI, Ono K, Iwamura Y, et al. Suppression of subgingival bacteria by antimicrobial photodynamic therapy using transgingival irradiation: A randomized clinical trial. J Periodontol. 2024;95(8):718-728. doi:10.1002/JPER.23-0328 64. Castillo, Y., Castellanos, J. E., Lafaurie, G. I., & Castillo, D. M. (2022). Porphyromonas gingivalis outer membrane vesicles modulate cytokine and chemokine production by gingipain-dependent mechanisms in human macrophages. Archives of oral biology, 140, 105453. https://doi.org/10.1016/j.archoralbio.2022.105453 65. Ministerio de Salud y Protección Social. 1993. Colombia. Resolución 008430 de 1993 por la que se establecen las normas científicas, técnicas y administrativas para la investigación en salud Título IV. Capítulo 1. Disponible en: https://www.minsalud.gov.co/sites/rid/Lists/BibliotecaDigital/RIDE/DE/DIJ/RESOLUCION-8430-DE-1993.PDF 66. Zhang W, Swearingen EB, Ju J, Rigney T, Tribble GD. Porphyromonas gingivalis invades osteoblasts and inhibits bone formation. Microbes Infect [Internet]. 2010;12(11):838–45. Disponible en: http://dx.doi.org/10.1016/j.micinf.2010.05.011 67. Wen Y, Dong H, Lin J, et al. Response of Human Gingival Fibroblasts and Porphyromonas gingivalis to UVC-Activated Titanium Surfaces. J Funct Biomater. 2023;14(3):137. Published 2023 Feb 28. doi:10.3390/jfb14030137 68. Xu LN, Yu XY, Chen WQ, Zhang SM, Qiu J. Biocorrosion of pure and SLA titanium surfaces in the presence of Porphyromonas gingivalis and its effects on osteoblast behavior. RSC Adv. 2020;10(14):8198-8206. Published 2020 Feb 25. doi:10.1039/d0ra00154f |
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Vargas Sánchez, PaulaCastillo Perdomo, DianaMuriel Rios, Mariana2024-12-13T17:28:23Z2024-12-13T17:28:23Z2024-11https://hdl.handle.net/20.500.12495/13708instname:Universidad El Bosquereponame:Repositorio Institucional Universidad El Bosquerepourl:https://repositorio.unbosque.edu.coAntecedentes: La periodontitis es una enfermedad inflamatoria crónica, multifactorial, que afecta los tejidos de soporte dental, además es el resultado de la interacción de factores ambientales, bacterianos y del hospedador. Porphyromonas gingivalis es una de las bacterias más frecuentemente asociada con la periodontitis, entender los cambios que suceden cuando entra en contacto con los osteoblastos puede darnos bases para comprender los mecanismos de la progresión de esta enfermedad. La literatura reporta algunos estudios mostrando el efecto de P. gingivalis sobre los tejidos blandos, pero no se encuentran datos concluyentes sobre su efecto en las células óseas. Objetivo: Evaluar el efecto de dos cepas de P. gingivalis en la diferenciación de las células pre-osteoblásticas MC3T3-E1 subclón 14. Materiales y Métodos: Cepas de P. gingivalis ATCC 33277 y W83 fueron sembradas en agar Brucella suplementado durante 4 días en condiciones anaeróbicas a 37°C, pasado el tiempo se ajustaron inóculos en medio de cultivo celular sin antibiótico a 1 x 108, a partir de estos se ajustó cada MOI. Se cultivaron las células MC3T3-E1 subclón 14 (ATCC) y se colocaron en contacto durante 12 horas con las cepas de P. gingivalis previamente descritas (Control +, MOI 50, MOI 100, MOI 150 y Control -), cumplido este periodo de tiempo se evaluó la viabilidad celular con el ensayo de resarzurina. Posteriormente se evaluó la formación de nódulos mineralizados a los 14 y 17 días mediante el ensayo de rojo de alizarina para las concentraciones (MOI 50 y MOI 100). Los datos obtenidos se analizaron mediante ANOVA y post test de Tukey con un nivel de confianza del 95%. Resultados: La viabilidad celular de las células MC3T3-E1 disminuyó significativamente (p<0,0001) ante la exposición a las cepas P. gingivalis W83 y P. gingivalis 33277 MOI 50 y MOI 100. El ensayo de rojo de alizarina para P. gingivalis 33277 a los 14 y 17 días de exposición no mostró diferencias significativas entre los grupos (p=0,8672 y p=0,6950, respectivamente). Para la cepa P. gingivalis W83 hubo una disminución estadísticamente significativa a los 14 y 17 días de evaluación (p=0,0423 y p=0,0321 respectivamente). Conclusiones: Las células MC3T3-E1 expuestas a cepas de P. gingivalis W83 y P. gingivalis 33277 tuvieron una disminución de la viabilidad celular, pero solo las expuestas a la cepa P. gingivalis W83 presentaron disminución en la formación de matriz mineralizada.Grupo de Investigación UIBO – Unidad de Investigación Básica OralOdontólogoPregradoBackground: Periodontitis is an inflammatory, multifactorial disease that affects the dental support tissues, it is the result of the environmental, bacterial and host factors interaction. Porphyromonas gingivalis is one of the bacteria most frequently associated with periodontitis, understanding the changes that occur when it comes into contact with osteoblasts can give us a basis for understanding the progression mechanisms of this disease. Literature reports some studies about the effect of P. gingivalis on soft tissues, but there is no conclusive data on its effect on bone cells. The objective of this work was to evaluate the effect of two strains of Porphyromonas gingivalis on the differentiation of MC3T3-E1 subclone 14 pre-osteoblastic cells. Aim: To evaluate the effect of two strains of P. gingivalis on the differentiation of MC3T3-E1 subclone 14 pre-osteoblastic cells. Methods: P. gingivalis strains ATCC 33277 and W83 were sown on Brucella agar supplemented for 4 days under anaerobic conditions at 37°C. After that time, the inoculum was adjusted in cell culture medium without antibiotics to 1 x 108, from each MOI. MC3T3-E1 subclone 14 (ATCC) cells were cultured and placed in contact for 12 hours with the previously described P. gingivalis strains (Control +, MOI 50, MOI 100, MOI 150, and Control -), after this period, cell viability was evaluated with the resazurin assay. Subsequently, the formation of mineralized nodules was evaluated at 14 and 17 days using the alizarin red test for concentrations (MOI 50 and MOI 100). The data obtained were analyzed using ANOVA and Tukey's post-test with a confidence level of 95%. Results: The cell viability of MC3T3-E1 cells decreased significantly (p<0.0001) upon exposure to strains P. gingivalis W83 and P. gingivalis 33277 MOI 50 and MOI 100. The alizarin red assay for P. gingivalis 33277 at 14 and 17 days of exposure did not show significant differences between the groups (p=0.8672 and p=0.6950, respectively). For the P. gingivalis W83 strain, there was a statistically significant decrease at 14 and 17 days of evaluation (p=0.0423 and p=0.0321 respectively). Conclusions: MC3T3-E1 cells exposed to strains P. gingivalis W83 and P. gingivalis 33277 had a decrease in cell viability, and only those exposed to strain P. gingivalis W83 showed a decrease in the formation of mineralized matrix.application/pdfAttribution-NonCommercial-ShareAlike 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-sa/4.0/Acceso abiertohttps://purl.org/coar/access_right/c_abf2http://purl.org/coar/access_right/c_abf2OsteoblastosPorphyromonas gingivalisViabilidad celularMineralización celularOsteoblastsPorphyromonas gingivalisCell viabilityCell mineralizationWU 100Efecto de la Porphyromonas gingivalis sobre células pre-osteoblásticas MC3T3-E1Effect of Porphyromonas gingivalis on pre-osteoblastic cells MC3T3-E1OdontologíaUniversidad El BosqueFacultad de OdontologíaTesis/Trabajo de grado - Monografía - Pregradohttps://purl.org/coar/resource_type/c_7a1fhttp://purl.org/coar/resource_type/c_7a1finfo:eu-repo/semantics/bachelorThesishttps://purl.org/coar/version/c_970fb48d4fbd8a851. 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