Cargando…
Reprogramming diminishes retention of Mycobacterium leprae in Schwann cells and elevates bacterial transfer property to fibroblasts
Background: Bacterial pathogens can manipulate or subvert host tissue cells to their advantage at different stages during infection, from initial colonization in primary host niches to dissemination. Recently, we have shown that Mycobacterium leprae (ML), the causative agent of human leprosy, reprog...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000Research
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3829123/ https://www.ncbi.nlm.nih.gov/pubmed/24358891 http://dx.doi.org/10.12688/f1000research.2-198.v3 |
_version_ | 1782291327324520448 |
---|---|
author | Masaki, Toshihiro McGlinchey, Aidan Tomlinson, Simon R. Qu, Jinrong Rambukkana, Anura |
author_facet | Masaki, Toshihiro McGlinchey, Aidan Tomlinson, Simon R. Qu, Jinrong Rambukkana, Anura |
author_sort | Masaki, Toshihiro |
collection | PubMed |
description | Background: Bacterial pathogens can manipulate or subvert host tissue cells to their advantage at different stages during infection, from initial colonization in primary host niches to dissemination. Recently, we have shown that Mycobacterium leprae (ML), the causative agent of human leprosy, reprogrammed its preferred host niche de-differentiated adult Schwann cells to progenitor/stem cell-like cells (pSLC) which appear to facilitate bacterial spread. Here, we studied how this cell fate change influences bacterial retention and transfer properties of Schwann cells before and after reprogramming. Results: Using primary fibroblasts as bacterial recipient cells, we showed that non-reprogrammed Schwann cells, which preserve all Schwann cell lineage and differentiation markers, possess high bacterial retention capacity when co-cultured with skin fibroblasts; Schwann cells failed to transfer bacteria to fibroblasts at higher numbers even after co-culture for 5 days. In contrast, pSLCs, which are derived from the same Schwann cells but have lost Schwann cell lineage markers due to reprogramming, efficiently transferred bacteria to fibroblasts within 24 hours. Conclusions: ML-induced reprogramming converts lineage-committed Schwann cells with high bacterial retention capacity to a cell type with pSLC stage with effective bacterial transfer properties. We propose that such changes in cellular properties may be associated with the initial intracellular colonization, which requires long-term bacterial retention within Schwann cells, in order to spread the infection to other tissues, which entails efficient bacterial transfer capacity to cells like fibroblasts which are abundant in many tissues, thereby potentially maximizing bacterial dissemination. These data also suggest how pathogens could take advantage of multiple facets of host cell reprogramming according to their needs during infection. |
format | Online Article Text |
id | pubmed-3829123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | F1000Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-38291232013-12-05 Reprogramming diminishes retention of Mycobacterium leprae in Schwann cells and elevates bacterial transfer property to fibroblasts Masaki, Toshihiro McGlinchey, Aidan Tomlinson, Simon R. Qu, Jinrong Rambukkana, Anura F1000Res Short Research Article Background: Bacterial pathogens can manipulate or subvert host tissue cells to their advantage at different stages during infection, from initial colonization in primary host niches to dissemination. Recently, we have shown that Mycobacterium leprae (ML), the causative agent of human leprosy, reprogrammed its preferred host niche de-differentiated adult Schwann cells to progenitor/stem cell-like cells (pSLC) which appear to facilitate bacterial spread. Here, we studied how this cell fate change influences bacterial retention and transfer properties of Schwann cells before and after reprogramming. Results: Using primary fibroblasts as bacterial recipient cells, we showed that non-reprogrammed Schwann cells, which preserve all Schwann cell lineage and differentiation markers, possess high bacterial retention capacity when co-cultured with skin fibroblasts; Schwann cells failed to transfer bacteria to fibroblasts at higher numbers even after co-culture for 5 days. In contrast, pSLCs, which are derived from the same Schwann cells but have lost Schwann cell lineage markers due to reprogramming, efficiently transferred bacteria to fibroblasts within 24 hours. Conclusions: ML-induced reprogramming converts lineage-committed Schwann cells with high bacterial retention capacity to a cell type with pSLC stage with effective bacterial transfer properties. We propose that such changes in cellular properties may be associated with the initial intracellular colonization, which requires long-term bacterial retention within Schwann cells, in order to spread the infection to other tissues, which entails efficient bacterial transfer capacity to cells like fibroblasts which are abundant in many tissues, thereby potentially maximizing bacterial dissemination. These data also suggest how pathogens could take advantage of multiple facets of host cell reprogramming according to their needs during infection. F1000Research 2013-11-14 /pmc/articles/PMC3829123/ /pubmed/24358891 http://dx.doi.org/10.12688/f1000research.2-198.v3 Text en Copyright: © 2013 Masaki T et al. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/publicdomain/zero/1.0/ Data associated with the article are available under the terms of the Creative Commons Zero "No rights reserved" data waiver (CC0 1.0 Public domain dedication). |
spellingShingle | Short Research Article Masaki, Toshihiro McGlinchey, Aidan Tomlinson, Simon R. Qu, Jinrong Rambukkana, Anura Reprogramming diminishes retention of Mycobacterium leprae in Schwann cells and elevates bacterial transfer property to fibroblasts |
title | Reprogramming diminishes retention of
Mycobacterium leprae in Schwann cells and elevates bacterial transfer property to fibroblasts |
title_full | Reprogramming diminishes retention of
Mycobacterium leprae in Schwann cells and elevates bacterial transfer property to fibroblasts |
title_fullStr | Reprogramming diminishes retention of
Mycobacterium leprae in Schwann cells and elevates bacterial transfer property to fibroblasts |
title_full_unstemmed | Reprogramming diminishes retention of
Mycobacterium leprae in Schwann cells and elevates bacterial transfer property to fibroblasts |
title_short | Reprogramming diminishes retention of
Mycobacterium leprae in Schwann cells and elevates bacterial transfer property to fibroblasts |
title_sort | reprogramming diminishes retention of
mycobacterium leprae in schwann cells and elevates bacterial transfer property to fibroblasts |
topic | Short Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3829123/ https://www.ncbi.nlm.nih.gov/pubmed/24358891 http://dx.doi.org/10.12688/f1000research.2-198.v3 |
work_keys_str_mv | AT masakitoshihiro reprogrammingdiminishesretentionofmycobacteriumlepraeinschwanncellsandelevatesbacterialtransferpropertytofibroblasts AT mcglincheyaidan reprogrammingdiminishesretentionofmycobacteriumlepraeinschwanncellsandelevatesbacterialtransferpropertytofibroblasts AT tomlinsonsimonr reprogrammingdiminishesretentionofmycobacteriumlepraeinschwanncellsandelevatesbacterialtransferpropertytofibroblasts AT qujinrong reprogrammingdiminishesretentionofmycobacteriumlepraeinschwanncellsandelevatesbacterialtransferpropertytofibroblasts AT rambukkanaanura reprogrammingdiminishesretentionofmycobacteriumlepraeinschwanncellsandelevatesbacterialtransferpropertytofibroblasts |