Mathematical modeling reveals kinetics of lymphocyte recirculation in the whole organism.

The kinetics of recirculation of naive lymphocytes in the body has important implications for the speed at which local infections are detected and controlled by immune responses. With a help of a novel mathematical model, we analyze experimental data on migration of 51Cr-labeled thoracic duct lympho...

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Autores principales: Vitaly V Ganusov, Jeremy Auerbach
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Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2014
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Acceso en línea:https://doaj.org/article/2443936b56cd4baab1187f0f1d376ee3
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spelling oai:doaj.org-article:2443936b56cd4baab1187f0f1d376ee32021-11-18T05:52:52ZMathematical modeling reveals kinetics of lymphocyte recirculation in the whole organism.1553-734X1553-735810.1371/journal.pcbi.1003586https://doaj.org/article/2443936b56cd4baab1187f0f1d376ee32014-05-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24830705/?tool=EBIhttps://doaj.org/toc/1553-734Xhttps://doaj.org/toc/1553-7358The kinetics of recirculation of naive lymphocytes in the body has important implications for the speed at which local infections are detected and controlled by immune responses. With a help of a novel mathematical model, we analyze experimental data on migration of 51Cr-labeled thoracic duct lymphocytes (TDLs) via major lymphoid and nonlymphoid tissues of rats in the absence of systemic antigenic stimulation. We show that at any point of time, 95% of lymphocytes in the blood travel via capillaries in the lung or sinusoids of the liver and only 5% migrate to secondary lymphoid tissues such as lymph nodes, Peyer's patches, or the spleen. Interestingly, our analysis suggests that lymphocytes travel via lung capillaries and liver sinusoids at an extremely rapid rate with the average residence time in these tissues being less than 1 minute. The model also predicts a relatively short average residence time of TDLs in the spleen (2.5 hours) and a longer average residence time of TDLs in major lymph nodes and Peyer's patches (10 hours). Surprisingly, we find that the average residence time of lymphocytes is similar in lymph nodes draining the skin (subcutaneous LNs) or the gut (mesenteric LNs) or in Peyer's patches. Applying our model to an additional dataset on lymphocyte migration via resting and antigen-stimulated lymph nodes we find that enlargement of antigen-stimulated lymph nodes occurs mainly due to increased entrance rate of TDLs into the nodes and not due to decreased exit rate as has been suggested in some studies. Taken together, our analysis for the first time provides a comprehensive, systems view of recirculation kinetics of thoracic duct lymphocytes in the whole organism.Vitaly V GanusovJeremy AuerbachPublic Library of Science (PLoS)articleBiology (General)QH301-705.5ENPLoS Computational Biology, Vol 10, Iss 5, p e1003586 (2014)
institution DOAJ
collection DOAJ
language EN
topic Biology (General)
QH301-705.5
spellingShingle Biology (General)
QH301-705.5
Vitaly V Ganusov
Jeremy Auerbach
Mathematical modeling reveals kinetics of lymphocyte recirculation in the whole organism.
description The kinetics of recirculation of naive lymphocytes in the body has important implications for the speed at which local infections are detected and controlled by immune responses. With a help of a novel mathematical model, we analyze experimental data on migration of 51Cr-labeled thoracic duct lymphocytes (TDLs) via major lymphoid and nonlymphoid tissues of rats in the absence of systemic antigenic stimulation. We show that at any point of time, 95% of lymphocytes in the blood travel via capillaries in the lung or sinusoids of the liver and only 5% migrate to secondary lymphoid tissues such as lymph nodes, Peyer's patches, or the spleen. Interestingly, our analysis suggests that lymphocytes travel via lung capillaries and liver sinusoids at an extremely rapid rate with the average residence time in these tissues being less than 1 minute. The model also predicts a relatively short average residence time of TDLs in the spleen (2.5 hours) and a longer average residence time of TDLs in major lymph nodes and Peyer's patches (10 hours). Surprisingly, we find that the average residence time of lymphocytes is similar in lymph nodes draining the skin (subcutaneous LNs) or the gut (mesenteric LNs) or in Peyer's patches. Applying our model to an additional dataset on lymphocyte migration via resting and antigen-stimulated lymph nodes we find that enlargement of antigen-stimulated lymph nodes occurs mainly due to increased entrance rate of TDLs into the nodes and not due to decreased exit rate as has been suggested in some studies. Taken together, our analysis for the first time provides a comprehensive, systems view of recirculation kinetics of thoracic duct lymphocytes in the whole organism.
format article
author Vitaly V Ganusov
Jeremy Auerbach
author_facet Vitaly V Ganusov
Jeremy Auerbach
author_sort Vitaly V Ganusov
title Mathematical modeling reveals kinetics of lymphocyte recirculation in the whole organism.
title_short Mathematical modeling reveals kinetics of lymphocyte recirculation in the whole organism.
title_full Mathematical modeling reveals kinetics of lymphocyte recirculation in the whole organism.
title_fullStr Mathematical modeling reveals kinetics of lymphocyte recirculation in the whole organism.
title_full_unstemmed Mathematical modeling reveals kinetics of lymphocyte recirculation in the whole organism.
title_sort mathematical modeling reveals kinetics of lymphocyte recirculation in the whole organism.
publisher Public Library of Science (PLoS)
publishDate 2014
url https://doaj.org/article/2443936b56cd4baab1187f0f1d376ee3
work_keys_str_mv AT vitalyvganusov mathematicalmodelingrevealskineticsoflymphocyterecirculationinthewholeorganism
AT jeremyauerbach mathematicalmodelingrevealskineticsoflymphocyterecirculationinthewholeorganism
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