Generalized Lévy walks and the role of chemokines in migration of effector CD8+ T cells
T cells in the brains of Toxoplasma -infected mice are shown to move by Lévy-like walks. T cells walk the Lévy walk T cells are an important first point of contact between the immune system and invading pathogens. The currently accepted model of the early stages of the immune reaction, in which the...
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Veröffentlicht in: | Nature (London) 2012-06, Vol.486 (7404), p.545-548 |
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creator | Harris, Tajie H. Banigan, Edward J. Christian, David A. Konradt, Christoph Tait Wojno, Elia D. Norose, Kazumi Wilson, Emma H. John, Beena Weninger, Wolfgang Luster, Andrew D. Liu, Andrea J. Hunter, Christopher A. |
description | T cells in the brains of
Toxoplasma
-infected mice are shown to move by Lévy-like walks.
T cells walk the Lévy walk
T cells are an important first point of contact between the immune system and invading pathogens. The currently accepted model of the early stages of the immune reaction, in which the T cells encounter the invader, is that of a Brownian random walk. This paper reports the use of
in vivo
multiphoton microscopy to demonstrate that the chemokine CXCL10 enhances the ability of CD8
+
T cells to control the protozoon pathogen
Toxoplasma gondii
. Surprisingly, the
in vivo
imaging reveals that T cells in the brains of mice infected with
T. gondii
move not by Brownian-type motion but instead follow a Lévy walk pattern of runs punctuated by periodic pauses. Mathematical simulations suggest that this mode of movement increases the chances of finding targets at unknown locations.
Chemokines have a central role in regulating processes essential to the immune function of T cells
1
,
2
,
3
, such as their migration within lymphoid tissues and targeting of pathogens in sites of inflammation. Here we track T cells using multi-photon microscopy to demonstrate that the chemokine CXCL10 enhances the ability of CD8
+
T cells to control the pathogen
Toxoplasma gondii
in the brains of chronically infected mice. This chemokine boosts T-cell function in two different ways: it maintains the effector T-cell population in the brain and speeds up the average migration speed without changing the nature of the walk statistics. Notably, these statistics are not Brownian; rather, CD8
+
T-cell motility in the brain is well described by a generalized Lévy walk. According to our model, this unexpected feature enables T cells to find rare targets with more than an order of magnitude more efficiency than Brownian random walkers. Thus, CD8
+
T-cell behaviour is similar to Lévy strategies reported in organisms ranging from mussels to marine predators and monkeys
4
,
5
,
6
,
7
,
8
,
9
,
10
, and CXCL10 aids T cells in shortening the average time taken to find rare targets. |
doi_str_mv | 10.1038/nature11098 |
format | Article |
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Toxoplasma
-infected mice are shown to move by Lévy-like walks.
T cells walk the Lévy walk
T cells are an important first point of contact between the immune system and invading pathogens. The currently accepted model of the early stages of the immune reaction, in which the T cells encounter the invader, is that of a Brownian random walk. This paper reports the use of
in vivo
multiphoton microscopy to demonstrate that the chemokine CXCL10 enhances the ability of CD8
+
T cells to control the protozoon pathogen
Toxoplasma gondii
. Surprisingly, the
in vivo
imaging reveals that T cells in the brains of mice infected with
T. gondii
move not by Brownian-type motion but instead follow a Lévy walk pattern of runs punctuated by periodic pauses. Mathematical simulations suggest that this mode of movement increases the chances of finding targets at unknown locations.
Chemokines have a central role in regulating processes essential to the immune function of T cells
1
,
2
,
3
, such as their migration within lymphoid tissues and targeting of pathogens in sites of inflammation. Here we track T cells using multi-photon microscopy to demonstrate that the chemokine CXCL10 enhances the ability of CD8
+
T cells to control the pathogen
Toxoplasma gondii
in the brains of chronically infected mice. This chemokine boosts T-cell function in two different ways: it maintains the effector T-cell population in the brain and speeds up the average migration speed without changing the nature of the walk statistics. Notably, these statistics are not Brownian; rather, CD8
+
T-cell motility in the brain is well described by a generalized Lévy walk. According to our model, this unexpected feature enables T cells to find rare targets with more than an order of magnitude more efficiency than Brownian random walkers. Thus, CD8
+
T-cell behaviour is similar to Lévy strategies reported in organisms ranging from mussels to marine predators and monkeys
4
,
5
,
6
,
7
,
8
,
9
,
10
, and CXCL10 aids T cells in shortening the average time taken to find rare targets.</description><identifier>ISSN: 0028-0836</identifier><identifier>EISSN: 1476-4687</identifier><identifier>DOI: 10.1038/nature11098</identifier><identifier>PMID: 22722867</identifier><identifier>CODEN: NATUAS</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/250/127/98 ; 631/57 ; 631/80/84 ; Animals ; Biological and medical sciences ; Brain - immunology ; Brain - microbiology ; CD8-Positive T-Lymphocytes - cytology ; CD8-Positive T-Lymphocytes - immunology ; Cell Movement ; Chemokine CXCL10 - antagonists & inhibitors ; Chemokine CXCL10 - genetics ; Chemokine CXCL10 - immunology ; Female ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Genetics of the immune response ; Humanities and Social Sciences ; Immunobiology ; letter ; Ligands ; Male ; Mice ; Mice, Inbred C57BL ; Models, Immunological ; multidisciplinary ; Receptors, CXCR3 - genetics ; Receptors, CXCR3 - metabolism ; Science ; Science (multidisciplinary) ; Time Factors ; Toxoplasma - growth & development ; Toxoplasma - immunology</subject><ispartof>Nature (London), 2012-06, Vol.486 (7404), p.545-548</ispartof><rights>Springer Nature Limited 2012</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-c8accc0b839f7c94ae178a083c2b3530f1906e8a2cc6ec0ebd14c55ee7ef5e223</citedby><cites>FETCH-LOGICAL-c448t-c8accc0b839f7c94ae178a083c2b3530f1906e8a2cc6ec0ebd14c55ee7ef5e223</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,315,781,785,886,27929,27930</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26036577$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22722867$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Harris, Tajie H.</creatorcontrib><creatorcontrib>Banigan, Edward J.</creatorcontrib><creatorcontrib>Christian, David A.</creatorcontrib><creatorcontrib>Konradt, Christoph</creatorcontrib><creatorcontrib>Tait Wojno, Elia D.</creatorcontrib><creatorcontrib>Norose, Kazumi</creatorcontrib><creatorcontrib>Wilson, Emma H.</creatorcontrib><creatorcontrib>John, Beena</creatorcontrib><creatorcontrib>Weninger, Wolfgang</creatorcontrib><creatorcontrib>Luster, Andrew D.</creatorcontrib><creatorcontrib>Liu, Andrea J.</creatorcontrib><creatorcontrib>Hunter, Christopher A.</creatorcontrib><title>Generalized Lévy walks and the role of chemokines in migration of effector CD8+ T cells</title><title>Nature (London)</title><addtitle>Nature</addtitle><addtitle>Nature</addtitle><description>T cells in the brains of
Toxoplasma
-infected mice are shown to move by Lévy-like walks.
T cells walk the Lévy walk
T cells are an important first point of contact between the immune system and invading pathogens. The currently accepted model of the early stages of the immune reaction, in which the T cells encounter the invader, is that of a Brownian random walk. This paper reports the use of
in vivo
multiphoton microscopy to demonstrate that the chemokine CXCL10 enhances the ability of CD8
+
T cells to control the protozoon pathogen
Toxoplasma gondii
. Surprisingly, the
in vivo
imaging reveals that T cells in the brains of mice infected with
T. gondii
move not by Brownian-type motion but instead follow a Lévy walk pattern of runs punctuated by periodic pauses. Mathematical simulations suggest that this mode of movement increases the chances of finding targets at unknown locations.
Chemokines have a central role in regulating processes essential to the immune function of T cells
1
,
2
,
3
, such as their migration within lymphoid tissues and targeting of pathogens in sites of inflammation. Here we track T cells using multi-photon microscopy to demonstrate that the chemokine CXCL10 enhances the ability of CD8
+
T cells to control the pathogen
Toxoplasma gondii
in the brains of chronically infected mice. This chemokine boosts T-cell function in two different ways: it maintains the effector T-cell population in the brain and speeds up the average migration speed without changing the nature of the walk statistics. Notably, these statistics are not Brownian; rather, CD8
+
T-cell motility in the brain is well described by a generalized Lévy walk. According to our model, this unexpected feature enables T cells to find rare targets with more than an order of magnitude more efficiency than Brownian random walkers. Thus, CD8
+
T-cell behaviour is similar to Lévy strategies reported in organisms ranging from mussels to marine predators and monkeys
4
,
5
,
6
,
7
,
8
,
9
,
10
, and CXCL10 aids T cells in shortening the average time taken to find rare targets.</description><subject>631/250/127/98</subject><subject>631/57</subject><subject>631/80/84</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Brain - immunology</subject><subject>Brain - microbiology</subject><subject>CD8-Positive T-Lymphocytes - cytology</subject><subject>CD8-Positive T-Lymphocytes - immunology</subject><subject>Cell Movement</subject><subject>Chemokine CXCL10 - antagonists & inhibitors</subject><subject>Chemokine CXCL10 - genetics</subject><subject>Chemokine CXCL10 - immunology</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Genetics of the immune response</subject><subject>Humanities and Social Sciences</subject><subject>Immunobiology</subject><subject>letter</subject><subject>Ligands</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Models, Immunological</subject><subject>multidisciplinary</subject><subject>Receptors, CXCR3 - genetics</subject><subject>Receptors, CXCR3 - metabolism</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Time Factors</subject><subject>Toxoplasma - growth & development</subject><subject>Toxoplasma - immunology</subject><issn>0028-0836</issn><issn>1476-4687</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkUFvEzEQhS1ERdPCiTvyBQmpLNjrXdt7QUIB2kqRuBSJm-VMxonbXbvYu0XlH_V38MdwlFBaidMc3qc3M-8R8pKzd5wJ_T7YcUrIOev0EzLjjZJVI7V6SmaM1bpiWshDcpTzJWOs5ap5Rg7rWtW1lmpGvp9iwGR7_wtXdPH77uaW_rT9VaY2rOi4QZpijzQ6Chsc4pUPmKkPdPDrZEcfw1ZC5xDGmOj8kz6hFxSw7_NzcuBsn_HFfh6Tb18-X8zPqsXX0_P5x0UFTaPHCrQFALbUonMKusYiV9qWm6FeilYwxzsmUdsaQCIwXK54A22LqNC1WNfimHzY-V5PywFXgGEs75jr5Aebbk203jxWgt-YdbwxQmglmq4YvNkbpPhjwjyaweftCzZgnLLhrESlpOSqoCc7FFLMOaG7X8OZ2XZhHnRR6FcPL7tn_4ZfgNd7wGawvUs2gM__OMmEbNWWe7vjcpHCGpO5jFMKJdX_7v0DyVCj3g</recordid><startdate>20120628</startdate><enddate>20120628</enddate><creator>Harris, Tajie H.</creator><creator>Banigan, Edward J.</creator><creator>Christian, David A.</creator><creator>Konradt, Christoph</creator><creator>Tait Wojno, Elia D.</creator><creator>Norose, Kazumi</creator><creator>Wilson, Emma H.</creator><creator>John, Beena</creator><creator>Weninger, Wolfgang</creator><creator>Luster, Andrew D.</creator><creator>Liu, Andrea J.</creator><creator>Hunter, Christopher A.</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20120628</creationdate><title>Generalized Lévy walks and the role of chemokines in migration of effector CD8+ T cells</title><author>Harris, Tajie H. ; Banigan, Edward J. ; Christian, David A. ; Konradt, Christoph ; Tait Wojno, Elia D. ; Norose, Kazumi ; Wilson, Emma H. ; John, Beena ; Weninger, Wolfgang ; Luster, Andrew D. ; Liu, Andrea J. ; Hunter, Christopher A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-c8accc0b839f7c94ae178a083c2b3530f1906e8a2cc6ec0ebd14c55ee7ef5e223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>631/250/127/98</topic><topic>631/57</topic><topic>631/80/84</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Brain - immunology</topic><topic>Brain - microbiology</topic><topic>CD8-Positive T-Lymphocytes - cytology</topic><topic>CD8-Positive T-Lymphocytes - immunology</topic><topic>Cell Movement</topic><topic>Chemokine CXCL10 - antagonists & inhibitors</topic><topic>Chemokine CXCL10 - genetics</topic><topic>Chemokine CXCL10 - immunology</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Genetics of the immune response</topic><topic>Humanities and Social Sciences</topic><topic>Immunobiology</topic><topic>letter</topic><topic>Ligands</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Models, Immunological</topic><topic>multidisciplinary</topic><topic>Receptors, CXCR3 - genetics</topic><topic>Receptors, CXCR3 - metabolism</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Time Factors</topic><topic>Toxoplasma - growth & development</topic><topic>Toxoplasma - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Harris, Tajie H.</creatorcontrib><creatorcontrib>Banigan, Edward J.</creatorcontrib><creatorcontrib>Christian, David A.</creatorcontrib><creatorcontrib>Konradt, Christoph</creatorcontrib><creatorcontrib>Tait Wojno, Elia D.</creatorcontrib><creatorcontrib>Norose, Kazumi</creatorcontrib><creatorcontrib>Wilson, Emma H.</creatorcontrib><creatorcontrib>John, Beena</creatorcontrib><creatorcontrib>Weninger, Wolfgang</creatorcontrib><creatorcontrib>Luster, Andrew D.</creatorcontrib><creatorcontrib>Liu, Andrea J.</creatorcontrib><creatorcontrib>Hunter, Christopher A.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nature (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Harris, Tajie H.</au><au>Banigan, Edward J.</au><au>Christian, David A.</au><au>Konradt, Christoph</au><au>Tait Wojno, Elia D.</au><au>Norose, Kazumi</au><au>Wilson, Emma H.</au><au>John, Beena</au><au>Weninger, Wolfgang</au><au>Luster, Andrew D.</au><au>Liu, Andrea J.</au><au>Hunter, Christopher A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Generalized Lévy walks and the role of chemokines in migration of effector CD8+ T cells</atitle><jtitle>Nature (London)</jtitle><stitle>Nature</stitle><addtitle>Nature</addtitle><date>2012-06-28</date><risdate>2012</risdate><volume>486</volume><issue>7404</issue><spage>545</spage><epage>548</epage><pages>545-548</pages><issn>0028-0836</issn><eissn>1476-4687</eissn><coden>NATUAS</coden><abstract>T cells in the brains of
Toxoplasma
-infected mice are shown to move by Lévy-like walks.
T cells walk the Lévy walk
T cells are an important first point of contact between the immune system and invading pathogens. The currently accepted model of the early stages of the immune reaction, in which the T cells encounter the invader, is that of a Brownian random walk. This paper reports the use of
in vivo
multiphoton microscopy to demonstrate that the chemokine CXCL10 enhances the ability of CD8
+
T cells to control the protozoon pathogen
Toxoplasma gondii
. Surprisingly, the
in vivo
imaging reveals that T cells in the brains of mice infected with
T. gondii
move not by Brownian-type motion but instead follow a Lévy walk pattern of runs punctuated by periodic pauses. Mathematical simulations suggest that this mode of movement increases the chances of finding targets at unknown locations.
Chemokines have a central role in regulating processes essential to the immune function of T cells
1
,
2
,
3
, such as their migration within lymphoid tissues and targeting of pathogens in sites of inflammation. Here we track T cells using multi-photon microscopy to demonstrate that the chemokine CXCL10 enhances the ability of CD8
+
T cells to control the pathogen
Toxoplasma gondii
in the brains of chronically infected mice. This chemokine boosts T-cell function in two different ways: it maintains the effector T-cell population in the brain and speeds up the average migration speed without changing the nature of the walk statistics. Notably, these statistics are not Brownian; rather, CD8
+
T-cell motility in the brain is well described by a generalized Lévy walk. According to our model, this unexpected feature enables T cells to find rare targets with more than an order of magnitude more efficiency than Brownian random walkers. Thus, CD8
+
T-cell behaviour is similar to Lévy strategies reported in organisms ranging from mussels to marine predators and monkeys
4
,
5
,
6
,
7
,
8
,
9
,
10
, and CXCL10 aids T cells in shortening the average time taken to find rare targets.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>22722867</pmid><doi>10.1038/nature11098</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 631/250/127/98 631/57 631/80/84 Animals Biological and medical sciences Brain - immunology Brain - microbiology CD8-Positive T-Lymphocytes - cytology CD8-Positive T-Lymphocytes - immunology Cell Movement Chemokine CXCL10 - antagonists & inhibitors Chemokine CXCL10 - genetics Chemokine CXCL10 - immunology Female Fundamental and applied biological sciences. Psychology Fundamental immunology Genetics of the immune response Humanities and Social Sciences Immunobiology letter Ligands Male Mice Mice, Inbred C57BL Models, Immunological multidisciplinary Receptors, CXCR3 - genetics Receptors, CXCR3 - metabolism Science Science (multidisciplinary) Time Factors Toxoplasma - growth & development Toxoplasma - immunology |
title | Generalized Lévy walks and the role of chemokines in migration of effector CD8+ T cells |
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