Cargando…
Modeling tuberculosis pathogenesis through ex vivo lung tissue infection
Tuberculosis (TB) is one of the top 10 causes of death worldwide. Several in vitro and in vivo experimental models have been used to study TB pathogenesis and induction of immune response during Mycobacterium tuberculosis infection. Precision cut lung tissue slices (PCLTS) is an experimental model,...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7106348/ https://www.ncbi.nlm.nih.gov/pubmed/29050759 http://dx.doi.org/10.1016/j.tube.2017.09.002 |
_version_ | 1783512592941056000 |
---|---|
author | Carranza-Rosales, Pilar Carranza-Torres, Irma Edith Guzmán-Delgado, Nancy Elena Lozano-Garza, Gerardo Villarreal-Treviño, Licet Molina-Torres, Carmen Villarreal, Javier Vargas Vera-Cabrera, Lucio Castro-Garza, Jorge |
author_facet | Carranza-Rosales, Pilar Carranza-Torres, Irma Edith Guzmán-Delgado, Nancy Elena Lozano-Garza, Gerardo Villarreal-Treviño, Licet Molina-Torres, Carmen Villarreal, Javier Vargas Vera-Cabrera, Lucio Castro-Garza, Jorge |
author_sort | Carranza-Rosales, Pilar |
collection | PubMed |
description | Tuberculosis (TB) is one of the top 10 causes of death worldwide. Several in vitro and in vivo experimental models have been used to study TB pathogenesis and induction of immune response during Mycobacterium tuberculosis infection. Precision cut lung tissue slices (PCLTS) is an experimental model, in which all the usual cell types of the organ are found, the tissue architecture and the interactions amongst the different cells are maintained. PCLTS in good physiological conditions, monitored by MTT assay and histology, were infected with either virulent Mycobacterium tuberculosis strain H37Rv or the TB vaccine strain Mycobacterium bovis BCG. Histological analysis showed that bacilli infecting lung tissue slices were observed in the alveolar septa, alveolar light spaces, near to type II pneumocytes, and inside macrophages. Mycobacterial infection of PCLTS induced TNF-α production, which is consistent with previous M. tuberculosis in vitro and in vivo studies. This is the first report of using PCLTS as a system to study M. tuberculosis infection. The PCLTS model provides a useful tool to evaluate the innate immune responses and other aspects during the early stages of mycobacterial infection. |
format | Online Article Text |
id | pubmed-7106348 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71063482020-03-31 Modeling tuberculosis pathogenesis through ex vivo lung tissue infection Carranza-Rosales, Pilar Carranza-Torres, Irma Edith Guzmán-Delgado, Nancy Elena Lozano-Garza, Gerardo Villarreal-Treviño, Licet Molina-Torres, Carmen Villarreal, Javier Vargas Vera-Cabrera, Lucio Castro-Garza, Jorge Tuberculosis (Edinb) Article Tuberculosis (TB) is one of the top 10 causes of death worldwide. Several in vitro and in vivo experimental models have been used to study TB pathogenesis and induction of immune response during Mycobacterium tuberculosis infection. Precision cut lung tissue slices (PCLTS) is an experimental model, in which all the usual cell types of the organ are found, the tissue architecture and the interactions amongst the different cells are maintained. PCLTS in good physiological conditions, monitored by MTT assay and histology, were infected with either virulent Mycobacterium tuberculosis strain H37Rv or the TB vaccine strain Mycobacterium bovis BCG. Histological analysis showed that bacilli infecting lung tissue slices were observed in the alveolar septa, alveolar light spaces, near to type II pneumocytes, and inside macrophages. Mycobacterial infection of PCLTS induced TNF-α production, which is consistent with previous M. tuberculosis in vitro and in vivo studies. This is the first report of using PCLTS as a system to study M. tuberculosis infection. The PCLTS model provides a useful tool to evaluate the innate immune responses and other aspects during the early stages of mycobacterial infection. Elsevier Ltd. 2017-12 2017-09-12 /pmc/articles/PMC7106348/ /pubmed/29050759 http://dx.doi.org/10.1016/j.tube.2017.09.002 Text en © 2017 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Carranza-Rosales, Pilar Carranza-Torres, Irma Edith Guzmán-Delgado, Nancy Elena Lozano-Garza, Gerardo Villarreal-Treviño, Licet Molina-Torres, Carmen Villarreal, Javier Vargas Vera-Cabrera, Lucio Castro-Garza, Jorge Modeling tuberculosis pathogenesis through ex vivo lung tissue infection |
title | Modeling tuberculosis pathogenesis through ex vivo lung tissue infection |
title_full | Modeling tuberculosis pathogenesis through ex vivo lung tissue infection |
title_fullStr | Modeling tuberculosis pathogenesis through ex vivo lung tissue infection |
title_full_unstemmed | Modeling tuberculosis pathogenesis through ex vivo lung tissue infection |
title_short | Modeling tuberculosis pathogenesis through ex vivo lung tissue infection |
title_sort | modeling tuberculosis pathogenesis through ex vivo lung tissue infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7106348/ https://www.ncbi.nlm.nih.gov/pubmed/29050759 http://dx.doi.org/10.1016/j.tube.2017.09.002 |
work_keys_str_mv | AT carranzarosalespilar modelingtuberculosispathogenesisthroughexvivolungtissueinfection AT carranzatorresirmaedith modelingtuberculosispathogenesisthroughexvivolungtissueinfection AT guzmandelgadonancyelena modelingtuberculosispathogenesisthroughexvivolungtissueinfection AT lozanogarzagerardo modelingtuberculosispathogenesisthroughexvivolungtissueinfection AT villarrealtrevinolicet modelingtuberculosispathogenesisthroughexvivolungtissueinfection AT molinatorrescarmen modelingtuberculosispathogenesisthroughexvivolungtissueinfection AT villarrealjaviervargas modelingtuberculosispathogenesisthroughexvivolungtissueinfection AT veracabreralucio modelingtuberculosispathogenesisthroughexvivolungtissueinfection AT castrogarzajorge modelingtuberculosispathogenesisthroughexvivolungtissueinfection |