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A Novel Bacterial Artificial Chromosome-Transgenic Podoplanin–Cre Mouse Targets Lymphoid Organ Stromal Cells in vivo

Stromal cells provide the structural foundation of secondary lymphoid organs (SLOs), and regulate leukocyte access and cell migration within the different compartments of spleen and lymph nodes (LNs). Furthermore, several stromal cell subsets have been implied in shaping of T cell responses through...

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Autores principales: Onder, Lucas, Scandella, Elke, Chai, Qian, Firner, Sonja, Mayer, Christian T., Sparwasser, Tim, Thiel, Volker, Rülicke, Thomas, Ludewig, Burkhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342134/
https://www.ncbi.nlm.nih.gov/pubmed/22566840
http://dx.doi.org/10.3389/fimmu.2011.00050
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author Onder, Lucas
Scandella, Elke
Chai, Qian
Firner, Sonja
Mayer, Christian T.
Sparwasser, Tim
Thiel, Volker
Rülicke, Thomas
Ludewig, Burkhard
author_facet Onder, Lucas
Scandella, Elke
Chai, Qian
Firner, Sonja
Mayer, Christian T.
Sparwasser, Tim
Thiel, Volker
Rülicke, Thomas
Ludewig, Burkhard
author_sort Onder, Lucas
collection PubMed
description Stromal cells provide the structural foundation of secondary lymphoid organs (SLOs), and regulate leukocyte access and cell migration within the different compartments of spleen and lymph nodes (LNs). Furthermore, several stromal cell subsets have been implied in shaping of T cell responses through direct presentation of antigen. Despite significant gain of knowledge on the biology of different SLO-resident stromal cell subsets, their molecular and functional characterization has remained incomplete. To address this need, we have generated a bacterial artificial chromosome-transgenic mouse model that utilizes the podoplanin (pdpn) promoter to express the Cre-recombinase exclusively in stromal cells of SLOs. The characterization of the Pdpn–Cre mouse revealed transgene expression in subsets of fibroblastic reticular cells and lymphatic endothelial cells in LNs. Furthermore, the transgene facilitated the identification of a novel splenic perivascular stromal cell subpopulation that forms web-like structures around central arterioles. Assessment of the in vivo antigen expression in the genetically tagged stromal cells in Pdpn–Cre mice revealed activation of both MHC I and II-restricted TCR transgenic T cells. Taken together, stromal pdpn–Cre expression is well-suited to characterize the phenotype and to dissect the function of lymphoid organ stromal cells.
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spelling pubmed-33421342012-05-07 A Novel Bacterial Artificial Chromosome-Transgenic Podoplanin–Cre Mouse Targets Lymphoid Organ Stromal Cells in vivo Onder, Lucas Scandella, Elke Chai, Qian Firner, Sonja Mayer, Christian T. Sparwasser, Tim Thiel, Volker Rülicke, Thomas Ludewig, Burkhard Front Immunol Immunology Stromal cells provide the structural foundation of secondary lymphoid organs (SLOs), and regulate leukocyte access and cell migration within the different compartments of spleen and lymph nodes (LNs). Furthermore, several stromal cell subsets have been implied in shaping of T cell responses through direct presentation of antigen. Despite significant gain of knowledge on the biology of different SLO-resident stromal cell subsets, their molecular and functional characterization has remained incomplete. To address this need, we have generated a bacterial artificial chromosome-transgenic mouse model that utilizes the podoplanin (pdpn) promoter to express the Cre-recombinase exclusively in stromal cells of SLOs. The characterization of the Pdpn–Cre mouse revealed transgene expression in subsets of fibroblastic reticular cells and lymphatic endothelial cells in LNs. Furthermore, the transgene facilitated the identification of a novel splenic perivascular stromal cell subpopulation that forms web-like structures around central arterioles. Assessment of the in vivo antigen expression in the genetically tagged stromal cells in Pdpn–Cre mice revealed activation of both MHC I and II-restricted TCR transgenic T cells. Taken together, stromal pdpn–Cre expression is well-suited to characterize the phenotype and to dissect the function of lymphoid organ stromal cells. Frontiers Research Foundation 2011-10-12 /pmc/articles/PMC3342134/ /pubmed/22566840 http://dx.doi.org/10.3389/fimmu.2011.00050 Text en Copyright © 2011 Onder, Scandella, Chai, Firner, Mayer, Sparwasser, Thiel, Rülicke and Ludewig. http://www.frontiersin.org/licenseagreement This is an open-access article subject to a non-exclusive license between the authors and Frontiers Media SA, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and other Frontiers conditions are complied with.
spellingShingle Immunology
Onder, Lucas
Scandella, Elke
Chai, Qian
Firner, Sonja
Mayer, Christian T.
Sparwasser, Tim
Thiel, Volker
Rülicke, Thomas
Ludewig, Burkhard
A Novel Bacterial Artificial Chromosome-Transgenic Podoplanin–Cre Mouse Targets Lymphoid Organ Stromal Cells in vivo
title A Novel Bacterial Artificial Chromosome-Transgenic Podoplanin–Cre Mouse Targets Lymphoid Organ Stromal Cells in vivo
title_full A Novel Bacterial Artificial Chromosome-Transgenic Podoplanin–Cre Mouse Targets Lymphoid Organ Stromal Cells in vivo
title_fullStr A Novel Bacterial Artificial Chromosome-Transgenic Podoplanin–Cre Mouse Targets Lymphoid Organ Stromal Cells in vivo
title_full_unstemmed A Novel Bacterial Artificial Chromosome-Transgenic Podoplanin–Cre Mouse Targets Lymphoid Organ Stromal Cells in vivo
title_short A Novel Bacterial Artificial Chromosome-Transgenic Podoplanin–Cre Mouse Targets Lymphoid Organ Stromal Cells in vivo
title_sort novel bacterial artificial chromosome-transgenic podoplanin–cre mouse targets lymphoid organ stromal cells in vivo
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342134/
https://www.ncbi.nlm.nih.gov/pubmed/22566840
http://dx.doi.org/10.3389/fimmu.2011.00050
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