Stromal IFN-γR-Signaling Modulates Goblet Cell Function During Salmonella Typhimurium Infection

Verfasser / Beitragende:
[Pascal Songhet, Manja Barthel, Bärbel Stecher, Andreas J. Müller, Markus Kremer, Gunnar C. Hansson, Wolf-Dietrich; id_orcid 0000-0002-9892-6420 Hardt]
Ort, Verlag, Jahr:
2011
Enthalten in:
PLoS ONE, 6 (7), p. e22459
Format:
Artikel (online)
ID: 528784463
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024 7 0 |a 10.3929/ethz-b-000038573  |2 doi 
024 7 0 |a 10.1371/journal.pone.0022459  |2 doi 
035 |a (ETHRESEARCH)oai:www.research-collecti.ethz.ch:20.500.11850/38573 
245 0 0 |a Stromal IFN-γR-Signaling Modulates Goblet Cell Function During Salmonella Typhimurium Infection  |h [Elektronische Daten]  |c [Pascal Songhet, Manja Barthel, Bärbel Stecher, Andreas J. Müller, Markus Kremer, Gunnar C. Hansson, Wolf-Dietrich; id_orcid 0000-0002-9892-6420 Hardt] 
246 0 |a PLoS ONE 
506 |a Open access  |2 ethresearch 
520 3 |a Enteropathogenic bacteria are a frequent cause of diarrhea worldwide. The mucosal defenses against infection are not completely understood. We have used the streptomycin mouse model for Salmonella Typhimurium diarrhea to analyze the role of interferon gamma receptor (IFN-γR)-signaling in mucosal defense. IFN-γ is known to contribute to acute S. Typhimurium diarrhea. We have compared the acute mucosal inflammation in IFN-γR-/- mice and wild type animals. IFN-γR-/- mice harbored increased pathogen loads in the mucosal epithelium and the lamina propria. Surprisingly, the epithelium of the IFN-γR-/- mice did not show the dramatic "loss” of mucus-filled goblet cell vacuoles, a hallmark of the wild type mucosal infection. Using bone marrow chimeric mice we established that IFN-γR-signaling in stromal cells (e.g. goblet cells, enterocytes) controlled mucus excretion/vacuole loss by goblet cells. In contrast, IFN-γR-signaling in bone marrow-derived cells (e.g. macrophages, DCs, PMNs) was required for restricting pathogen growth in the gut tissue. Thus IFN-γR-signaling influences different mucosal responses to infection, including not only pathogen restriction in the lamina propria, but, as shown here, also goblet cell function. 
540 |a Creative Commons Attribution 3.0 Unported  |u http://creativecommons.org/licenses/by/3.0  |2 ethresearch 
700 1 |a Songhet  |D Pascal  |e joint author 
700 1 |a Barthel  |D Manja  |e joint author 
700 1 |a Stecher  |D Bärbel  |e joint author 
700 1 |a Müller  |D Andreas J.  |e joint author 
700 1 |a Kremer  |D Markus  |e joint author 
700 1 |a Hansson  |D Gunnar C.  |e joint author 
700 1 |a Hardt  |D Wolf-Dietrich; id_orcid 0000-0002-9892-6420  |e joint author 
773 0 |t PLoS ONE  |d Lawrence, KS, USA : Public Library of Science  |g 6 (7), p. e22459  |x 1932-6203 
856 4 0 |u http://hdl.handle.net/20.500.11850/38573  |q text/html  |z WWW-Backlink auf das Repository (Open access) 
908 |D 1  |a Journal Article  |2 ethresearch 
950 |B ETHRESEARCH  |P 856  |E 40  |u http://hdl.handle.net/20.500.11850/38573  |q text/html  |z WWW-Backlink auf das Repository (Open access) 
950 |B ETHRESEARCH  |P 700  |E 1-  |a Songhet  |D Pascal  |e joint author 
950 |B ETHRESEARCH  |P 700  |E 1-  |a Barthel  |D Manja  |e joint author 
950 |B ETHRESEARCH  |P 700  |E 1-  |a Stecher  |D Bärbel  |e joint author 
950 |B ETHRESEARCH  |P 700  |E 1-  |a Müller  |D Andreas J.  |e joint author 
950 |B ETHRESEARCH  |P 700  |E 1-  |a Kremer  |D Markus  |e joint author 
950 |B ETHRESEARCH  |P 700  |E 1-  |a Hansson  |D Gunnar C.  |e joint author 
950 |B ETHRESEARCH  |P 700  |E 1-  |a Hardt  |D Wolf-Dietrich; id_orcid 0000-0002-9892-6420  |e joint author 
950 |B ETHRESEARCH  |P 773  |E 0-  |t PLoS ONE  |d Lawrence, KS, USA : Public Library of Science  |g 6 (7), p. e22459  |x 1932-6203 
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949 |B ETHRESEARCH  |F ETHRESEARCH  |b ETHRESEARCH  |j Journal Article  |c Open access