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A Conduit System Distributes Chemokines and Small Blood-borne Molecules through the Splenic White Pulp
Access to the splenic white pulp is restricted to lymphocytes and dendritic cells. Here we show that movement of molecules from the blood into these confined areas is also limited. Large molecules, such as bovine serum albumin (68 kD), immunoglobulin G (150 kD), and 500 kD dextran are unable to ente...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2003
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2194088/ https://www.ncbi.nlm.nih.gov/pubmed/12900524 http://dx.doi.org/10.1084/jem.20021801 |
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author | Nolte, Martijn A. Beliën, Jeroen A.M. Schadee-Eestermans, Inge Jansen, Wendy Unger, Wendy W.J. van Rooijen, Nico Kraal, Georg Mebius, Reina E. |
author_facet | Nolte, Martijn A. Beliën, Jeroen A.M. Schadee-Eestermans, Inge Jansen, Wendy Unger, Wendy W.J. van Rooijen, Nico Kraal, Georg Mebius, Reina E. |
author_sort | Nolte, Martijn A. |
collection | PubMed |
description | Access to the splenic white pulp is restricted to lymphocytes and dendritic cells. Here we show that movement of molecules from the blood into these confined areas is also limited. Large molecules, such as bovine serum albumin (68 kD), immunoglobulin G (150 kD), and 500 kD dextran are unable to enter the white pulp, whereas smaller blood-borne molecules can directly permeate this compartment. The distribution is restricted to a stromal network that we refer to as the splenic conduit system. The small lumen of the conduit contains collagen fibers and is surrounded in the T cell areas by reticular fibroblasts that express ER-TR7. It also contains the chemokine CCL21. Conversely, in B cell follicles the B cell–attracting chemokine CXCL13 was found to be associated with the conduit and absence of ER-TR7(+) fibroblasts. These results show heterogeneity of reticular fibroblasts that enfold the conduit system and suggest that locally produced chemokines are transported through and presented on this reticular network. Therefore, the conduit plays a role in distribution of both blood-borne and locally produced molecules and provides a framework for directing lymphocyte migration and organization of the splenic white pulp. |
format | Text |
id | pubmed-2194088 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21940882008-04-11 A Conduit System Distributes Chemokines and Small Blood-borne Molecules through the Splenic White Pulp Nolte, Martijn A. Beliën, Jeroen A.M. Schadee-Eestermans, Inge Jansen, Wendy Unger, Wendy W.J. van Rooijen, Nico Kraal, Georg Mebius, Reina E. J Exp Med Brief Definitive Report Access to the splenic white pulp is restricted to lymphocytes and dendritic cells. Here we show that movement of molecules from the blood into these confined areas is also limited. Large molecules, such as bovine serum albumin (68 kD), immunoglobulin G (150 kD), and 500 kD dextran are unable to enter the white pulp, whereas smaller blood-borne molecules can directly permeate this compartment. The distribution is restricted to a stromal network that we refer to as the splenic conduit system. The small lumen of the conduit contains collagen fibers and is surrounded in the T cell areas by reticular fibroblasts that express ER-TR7. It also contains the chemokine CCL21. Conversely, in B cell follicles the B cell–attracting chemokine CXCL13 was found to be associated with the conduit and absence of ER-TR7(+) fibroblasts. These results show heterogeneity of reticular fibroblasts that enfold the conduit system and suggest that locally produced chemokines are transported through and presented on this reticular network. Therefore, the conduit plays a role in distribution of both blood-borne and locally produced molecules and provides a framework for directing lymphocyte migration and organization of the splenic white pulp. The Rockefeller University Press 2003-08-04 /pmc/articles/PMC2194088/ /pubmed/12900524 http://dx.doi.org/10.1084/jem.20021801 Text en Copyright © 2003, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Brief Definitive Report Nolte, Martijn A. Beliën, Jeroen A.M. Schadee-Eestermans, Inge Jansen, Wendy Unger, Wendy W.J. van Rooijen, Nico Kraal, Georg Mebius, Reina E. A Conduit System Distributes Chemokines and Small Blood-borne Molecules through the Splenic White Pulp |
title | A Conduit System Distributes Chemokines and Small Blood-borne Molecules through the Splenic White Pulp |
title_full | A Conduit System Distributes Chemokines and Small Blood-borne Molecules through the Splenic White Pulp |
title_fullStr | A Conduit System Distributes Chemokines and Small Blood-borne Molecules through the Splenic White Pulp |
title_full_unstemmed | A Conduit System Distributes Chemokines and Small Blood-borne Molecules through the Splenic White Pulp |
title_short | A Conduit System Distributes Chemokines and Small Blood-borne Molecules through the Splenic White Pulp |
title_sort | conduit system distributes chemokines and small blood-borne molecules through the splenic white pulp |
topic | Brief Definitive Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2194088/ https://www.ncbi.nlm.nih.gov/pubmed/12900524 http://dx.doi.org/10.1084/jem.20021801 |
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