A role for LFA‐1 in delaying T‐lymphocyte egress from lymph nodes
Abstract Lymphocytes use the integrin leukocyte function‐associated antigen‐1 (LFA‐1) to cross the vasculature into lymph nodes (LNs), but it has been uncertain whether their migration within LN is also LFA‐1 dependent. We show that LFA‐1 mediates prolonged LN residence as LFA‐1−/− CD4 T cells have...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Reichardt, Peter [verfasserIn] Patzak, Irene [verfasserIn] Jones, Kristian [verfasserIn] Etemire, Eloho [verfasserIn] Gunzer, Matthias [verfasserIn] Hogg, Nancy [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2013 |
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| Schlagwörter: |
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| Anmerkung: |
© European Molecular Biology Organization 2013 |
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| Übergeordnetes Werk: |
Enthalten in: The EMBO Journal - Nature Publishing Group UK, 2023, 32(2013), 6 vom: 26. Feb., Seite 829-843 |
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| Übergeordnetes Werk: |
volume:32 ; year:2013 ; number:6 ; day:26 ; month:02 ; pages:829-843 |
| Links: |
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| DOI / URN: |
10.1038/emboj.2013.33 |
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| Katalog-ID: |
SPR057956251 |
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| 245 | 1 | 0 | |a A role for LFA‐1 in delaying T‐lymphocyte egress from lymph nodes |
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| 520 | |a Abstract Lymphocytes use the integrin leukocyte function‐associated antigen‐1 (LFA‐1) to cross the vasculature into lymph nodes (LNs), but it has been uncertain whether their migration within LN is also LFA‐1 dependent. We show that LFA‐1 mediates prolonged LN residence as LFA‐1−/− CD4 T cells have significantly decreased dwell times compared with LFA‐1+/+ T cells, a distinction lost in hosts lacking the major LFA‐1 ligand ICAM‐1. Intra‐vital two‐photon microscopy revealed that LFA‐1+/+ and LFA‐1−/− T cells reacted differently when probing the ICAM‐1‐expressing lymphatic network. While LFA‐1+/+ T cells returned to the LN parenchyma with greater frequency, LFA‐1−/− T cells egressed promptly. This difference in exit behaviour was a feature of egress through all assessed lymphatic exit sites. We show that use of LFA‐1 as an adhesion receptor amplifies the number of T cells returning to the LN parenchyma that can lead to increased effectiveness of T‐cell response to antigen. Thus, we identify a novel function for LFA‐1 in guiding T cells at the critical point of LN egress when they either exit or return into the LN for further interactions. | ||
| 520 | |a Abstract The integrin LFA‐1 mediates the adhesion of T cells to lymphatic vessels expressing the LFA‐1 ligand ICAM‐1, prolonging T‐cell retention in lymph nodes to increase their chances of encountering foreign antigens. | ||
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| 700 | 1 | |a Patzak, Irene |e verfasserin |4 aut | |
| 700 | 1 | |a Jones, Kristian |e verfasserin |4 aut | |
| 700 | 1 | |a Etemire, Eloho |e verfasserin |4 aut | |
| 700 | 1 | |a Gunzer, Matthias |e verfasserin |4 aut | |
| 700 | 1 | |a Hogg, Nancy |e verfasserin |4 aut | |
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10.1038/emboj.2013.33 doi (DE-627)SPR057956251 (SPR)emboj.2013.33-e DE-627 ger DE-627 rakwb eng Reichardt, Peter verfasserin aut A role for LFA‐1 in delaying T‐lymphocyte egress from lymph nodes 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Molecular Biology Organization 2013 Abstract Lymphocytes use the integrin leukocyte function‐associated antigen‐1 (LFA‐1) to cross the vasculature into lymph nodes (LNs), but it has been uncertain whether their migration within LN is also LFA‐1 dependent. We show that LFA‐1 mediates prolonged LN residence as LFA‐1−/− CD4 T cells have significantly decreased dwell times compared with LFA‐1+/+ T cells, a distinction lost in hosts lacking the major LFA‐1 ligand ICAM‐1. Intra‐vital two‐photon microscopy revealed that LFA‐1+/+ and LFA‐1−/− T cells reacted differently when probing the ICAM‐1‐expressing lymphatic network. While LFA‐1+/+ T cells returned to the LN parenchyma with greater frequency, LFA‐1−/− T cells egressed promptly. This difference in exit behaviour was a feature of egress through all assessed lymphatic exit sites. We show that use of LFA‐1 as an adhesion receptor amplifies the number of T cells returning to the LN parenchyma that can lead to increased effectiveness of T‐cell response to antigen. Thus, we identify a novel function for LFA‐1 in guiding T cells at the critical point of LN egress when they either exit or return into the LN for further interactions. Abstract The integrin LFA‐1 mediates the adhesion of T cells to lymphatic vessels expressing the LFA‐1 ligand ICAM‐1, prolonging T‐cell retention in lymph nodes to increase their chances of encountering foreign antigens. LFA‐1 (dpeaa)DE-He213 lymphatics (dpeaa)DE-He213 lymph node (dpeaa)DE-He213 migration (dpeaa)DE-He213 T cells (dpeaa)DE-He213 Patzak, Irene verfasserin aut Jones, Kristian verfasserin aut Etemire, Eloho verfasserin aut Gunzer, Matthias verfasserin aut Hogg, Nancy verfasserin aut Enthalten in The EMBO Journal Nature Publishing Group UK, 2023 32(2013), 6 vom: 26. Feb., Seite 829-843 (DE-627)266022529 (DE-600)1467419-1 1460-2075 nnns volume:32 year:2013 number:6 day:26 month:02 pages:829-843 https://dx.doi.org/10.1038/emboj.2013.33 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_72 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_252 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4116 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4155 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4313 GBV_ILN_4314 GBV_ILN_4318 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4598 GBV_ILN_4700 AR 32 2013 6 26 02 829-843 |
| spelling |
10.1038/emboj.2013.33 doi (DE-627)SPR057956251 (SPR)emboj.2013.33-e DE-627 ger DE-627 rakwb eng Reichardt, Peter verfasserin aut A role for LFA‐1 in delaying T‐lymphocyte egress from lymph nodes 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Molecular Biology Organization 2013 Abstract Lymphocytes use the integrin leukocyte function‐associated antigen‐1 (LFA‐1) to cross the vasculature into lymph nodes (LNs), but it has been uncertain whether their migration within LN is also LFA‐1 dependent. We show that LFA‐1 mediates prolonged LN residence as LFA‐1−/− CD4 T cells have significantly decreased dwell times compared with LFA‐1+/+ T cells, a distinction lost in hosts lacking the major LFA‐1 ligand ICAM‐1. Intra‐vital two‐photon microscopy revealed that LFA‐1+/+ and LFA‐1−/− T cells reacted differently when probing the ICAM‐1‐expressing lymphatic network. While LFA‐1+/+ T cells returned to the LN parenchyma with greater frequency, LFA‐1−/− T cells egressed promptly. This difference in exit behaviour was a feature of egress through all assessed lymphatic exit sites. We show that use of LFA‐1 as an adhesion receptor amplifies the number of T cells returning to the LN parenchyma that can lead to increased effectiveness of T‐cell response to antigen. Thus, we identify a novel function for LFA‐1 in guiding T cells at the critical point of LN egress when they either exit or return into the LN for further interactions. Abstract The integrin LFA‐1 mediates the adhesion of T cells to lymphatic vessels expressing the LFA‐1 ligand ICAM‐1, prolonging T‐cell retention in lymph nodes to increase their chances of encountering foreign antigens. LFA‐1 (dpeaa)DE-He213 lymphatics (dpeaa)DE-He213 lymph node (dpeaa)DE-He213 migration (dpeaa)DE-He213 T cells (dpeaa)DE-He213 Patzak, Irene verfasserin aut Jones, Kristian verfasserin aut Etemire, Eloho verfasserin aut Gunzer, Matthias verfasserin aut Hogg, Nancy verfasserin aut Enthalten in The EMBO Journal Nature Publishing Group UK, 2023 32(2013), 6 vom: 26. Feb., Seite 829-843 (DE-627)266022529 (DE-600)1467419-1 1460-2075 nnns volume:32 year:2013 number:6 day:26 month:02 pages:829-843 https://dx.doi.org/10.1038/emboj.2013.33 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_72 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_252 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4116 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4155 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4313 GBV_ILN_4314 GBV_ILN_4318 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4598 GBV_ILN_4700 AR 32 2013 6 26 02 829-843 |
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10.1038/emboj.2013.33 doi (DE-627)SPR057956251 (SPR)emboj.2013.33-e DE-627 ger DE-627 rakwb eng Reichardt, Peter verfasserin aut A role for LFA‐1 in delaying T‐lymphocyte egress from lymph nodes 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Molecular Biology Organization 2013 Abstract Lymphocytes use the integrin leukocyte function‐associated antigen‐1 (LFA‐1) to cross the vasculature into lymph nodes (LNs), but it has been uncertain whether their migration within LN is also LFA‐1 dependent. We show that LFA‐1 mediates prolonged LN residence as LFA‐1−/− CD4 T cells have significantly decreased dwell times compared with LFA‐1+/+ T cells, a distinction lost in hosts lacking the major LFA‐1 ligand ICAM‐1. Intra‐vital two‐photon microscopy revealed that LFA‐1+/+ and LFA‐1−/− T cells reacted differently when probing the ICAM‐1‐expressing lymphatic network. While LFA‐1+/+ T cells returned to the LN parenchyma with greater frequency, LFA‐1−/− T cells egressed promptly. This difference in exit behaviour was a feature of egress through all assessed lymphatic exit sites. We show that use of LFA‐1 as an adhesion receptor amplifies the number of T cells returning to the LN parenchyma that can lead to increased effectiveness of T‐cell response to antigen. Thus, we identify a novel function for LFA‐1 in guiding T cells at the critical point of LN egress when they either exit or return into the LN for further interactions. Abstract The integrin LFA‐1 mediates the adhesion of T cells to lymphatic vessels expressing the LFA‐1 ligand ICAM‐1, prolonging T‐cell retention in lymph nodes to increase their chances of encountering foreign antigens. LFA‐1 (dpeaa)DE-He213 lymphatics (dpeaa)DE-He213 lymph node (dpeaa)DE-He213 migration (dpeaa)DE-He213 T cells (dpeaa)DE-He213 Patzak, Irene verfasserin aut Jones, Kristian verfasserin aut Etemire, Eloho verfasserin aut Gunzer, Matthias verfasserin aut Hogg, Nancy verfasserin aut Enthalten in The EMBO Journal Nature Publishing Group UK, 2023 32(2013), 6 vom: 26. Feb., Seite 829-843 (DE-627)266022529 (DE-600)1467419-1 1460-2075 nnns volume:32 year:2013 number:6 day:26 month:02 pages:829-843 https://dx.doi.org/10.1038/emboj.2013.33 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_72 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_252 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4116 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4155 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4313 GBV_ILN_4314 GBV_ILN_4318 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4598 GBV_ILN_4700 AR 32 2013 6 26 02 829-843 |
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10.1038/emboj.2013.33 doi (DE-627)SPR057956251 (SPR)emboj.2013.33-e DE-627 ger DE-627 rakwb eng Reichardt, Peter verfasserin aut A role for LFA‐1 in delaying T‐lymphocyte egress from lymph nodes 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Molecular Biology Organization 2013 Abstract Lymphocytes use the integrin leukocyte function‐associated antigen‐1 (LFA‐1) to cross the vasculature into lymph nodes (LNs), but it has been uncertain whether their migration within LN is also LFA‐1 dependent. We show that LFA‐1 mediates prolonged LN residence as LFA‐1−/− CD4 T cells have significantly decreased dwell times compared with LFA‐1+/+ T cells, a distinction lost in hosts lacking the major LFA‐1 ligand ICAM‐1. Intra‐vital two‐photon microscopy revealed that LFA‐1+/+ and LFA‐1−/− T cells reacted differently when probing the ICAM‐1‐expressing lymphatic network. While LFA‐1+/+ T cells returned to the LN parenchyma with greater frequency, LFA‐1−/− T cells egressed promptly. This difference in exit behaviour was a feature of egress through all assessed lymphatic exit sites. We show that use of LFA‐1 as an adhesion receptor amplifies the number of T cells returning to the LN parenchyma that can lead to increased effectiveness of T‐cell response to antigen. Thus, we identify a novel function for LFA‐1 in guiding T cells at the critical point of LN egress when they either exit or return into the LN for further interactions. Abstract The integrin LFA‐1 mediates the adhesion of T cells to lymphatic vessels expressing the LFA‐1 ligand ICAM‐1, prolonging T‐cell retention in lymph nodes to increase their chances of encountering foreign antigens. LFA‐1 (dpeaa)DE-He213 lymphatics (dpeaa)DE-He213 lymph node (dpeaa)DE-He213 migration (dpeaa)DE-He213 T cells (dpeaa)DE-He213 Patzak, Irene verfasserin aut Jones, Kristian verfasserin aut Etemire, Eloho verfasserin aut Gunzer, Matthias verfasserin aut Hogg, Nancy verfasserin aut Enthalten in The EMBO Journal Nature Publishing Group UK, 2023 32(2013), 6 vom: 26. Feb., Seite 829-843 (DE-627)266022529 (DE-600)1467419-1 1460-2075 nnns volume:32 year:2013 number:6 day:26 month:02 pages:829-843 https://dx.doi.org/10.1038/emboj.2013.33 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_72 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_252 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4116 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4155 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4313 GBV_ILN_4314 GBV_ILN_4318 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4598 GBV_ILN_4700 AR 32 2013 6 26 02 829-843 |
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10.1038/emboj.2013.33 doi (DE-627)SPR057956251 (SPR)emboj.2013.33-e DE-627 ger DE-627 rakwb eng Reichardt, Peter verfasserin aut A role for LFA‐1 in delaying T‐lymphocyte egress from lymph nodes 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Molecular Biology Organization 2013 Abstract Lymphocytes use the integrin leukocyte function‐associated antigen‐1 (LFA‐1) to cross the vasculature into lymph nodes (LNs), but it has been uncertain whether their migration within LN is also LFA‐1 dependent. We show that LFA‐1 mediates prolonged LN residence as LFA‐1−/− CD4 T cells have significantly decreased dwell times compared with LFA‐1+/+ T cells, a distinction lost in hosts lacking the major LFA‐1 ligand ICAM‐1. Intra‐vital two‐photon microscopy revealed that LFA‐1+/+ and LFA‐1−/− T cells reacted differently when probing the ICAM‐1‐expressing lymphatic network. While LFA‐1+/+ T cells returned to the LN parenchyma with greater frequency, LFA‐1−/− T cells egressed promptly. This difference in exit behaviour was a feature of egress through all assessed lymphatic exit sites. We show that use of LFA‐1 as an adhesion receptor amplifies the number of T cells returning to the LN parenchyma that can lead to increased effectiveness of T‐cell response to antigen. Thus, we identify a novel function for LFA‐1 in guiding T cells at the critical point of LN egress when they either exit or return into the LN for further interactions. Abstract The integrin LFA‐1 mediates the adhesion of T cells to lymphatic vessels expressing the LFA‐1 ligand ICAM‐1, prolonging T‐cell retention in lymph nodes to increase their chances of encountering foreign antigens. LFA‐1 (dpeaa)DE-He213 lymphatics (dpeaa)DE-He213 lymph node (dpeaa)DE-He213 migration (dpeaa)DE-He213 T cells (dpeaa)DE-He213 Patzak, Irene verfasserin aut Jones, Kristian verfasserin aut Etemire, Eloho verfasserin aut Gunzer, Matthias verfasserin aut Hogg, Nancy verfasserin aut Enthalten in The EMBO Journal Nature Publishing Group UK, 2023 32(2013), 6 vom: 26. Feb., Seite 829-843 (DE-627)266022529 (DE-600)1467419-1 1460-2075 nnns volume:32 year:2013 number:6 day:26 month:02 pages:829-843 https://dx.doi.org/10.1038/emboj.2013.33 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_72 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_252 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4116 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4155 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4313 GBV_ILN_4314 GBV_ILN_4318 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4598 GBV_ILN_4700 AR 32 2013 6 26 02 829-843 |
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Enthalten in The EMBO Journal 32(2013), 6 vom: 26. Feb., Seite 829-843 volume:32 year:2013 number:6 day:26 month:02 pages:829-843 |
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Reichardt, Peter @@aut@@ Patzak, Irene @@aut@@ Jones, Kristian @@aut@@ Etemire, Eloho @@aut@@ Gunzer, Matthias @@aut@@ Hogg, Nancy @@aut@@ |
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Reichardt, Peter |
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Reichardt, Peter misc LFA‐1 misc lymphatics misc lymph node misc migration misc T cells A role for LFA‐1 in delaying T‐lymphocyte egress from lymph nodes |
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A role for LFA‐1 in delaying T‐lymphocyte egress from lymph nodes LFA‐1 (dpeaa)DE-He213 lymphatics (dpeaa)DE-He213 lymph node (dpeaa)DE-He213 migration (dpeaa)DE-He213 T cells (dpeaa)DE-He213 |
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a role for lfa‐1 in delaying t‐lymphocyte egress from lymph nodes |
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A role for LFA‐1 in delaying T‐lymphocyte egress from lymph nodes |
| abstract |
Abstract Lymphocytes use the integrin leukocyte function‐associated antigen‐1 (LFA‐1) to cross the vasculature into lymph nodes (LNs), but it has been uncertain whether their migration within LN is also LFA‐1 dependent. We show that LFA‐1 mediates prolonged LN residence as LFA‐1−/− CD4 T cells have significantly decreased dwell times compared with LFA‐1+/+ T cells, a distinction lost in hosts lacking the major LFA‐1 ligand ICAM‐1. Intra‐vital two‐photon microscopy revealed that LFA‐1+/+ and LFA‐1−/− T cells reacted differently when probing the ICAM‐1‐expressing lymphatic network. While LFA‐1+/+ T cells returned to the LN parenchyma with greater frequency, LFA‐1−/− T cells egressed promptly. This difference in exit behaviour was a feature of egress through all assessed lymphatic exit sites. We show that use of LFA‐1 as an adhesion receptor amplifies the number of T cells returning to the LN parenchyma that can lead to increased effectiveness of T‐cell response to antigen. Thus, we identify a novel function for LFA‐1 in guiding T cells at the critical point of LN egress when they either exit or return into the LN for further interactions. Abstract The integrin LFA‐1 mediates the adhesion of T cells to lymphatic vessels expressing the LFA‐1 ligand ICAM‐1, prolonging T‐cell retention in lymph nodes to increase their chances of encountering foreign antigens. © European Molecular Biology Organization 2013 |
| abstractGer |
Abstract Lymphocytes use the integrin leukocyte function‐associated antigen‐1 (LFA‐1) to cross the vasculature into lymph nodes (LNs), but it has been uncertain whether their migration within LN is also LFA‐1 dependent. We show that LFA‐1 mediates prolonged LN residence as LFA‐1−/− CD4 T cells have significantly decreased dwell times compared with LFA‐1+/+ T cells, a distinction lost in hosts lacking the major LFA‐1 ligand ICAM‐1. Intra‐vital two‐photon microscopy revealed that LFA‐1+/+ and LFA‐1−/− T cells reacted differently when probing the ICAM‐1‐expressing lymphatic network. While LFA‐1+/+ T cells returned to the LN parenchyma with greater frequency, LFA‐1−/− T cells egressed promptly. This difference in exit behaviour was a feature of egress through all assessed lymphatic exit sites. We show that use of LFA‐1 as an adhesion receptor amplifies the number of T cells returning to the LN parenchyma that can lead to increased effectiveness of T‐cell response to antigen. Thus, we identify a novel function for LFA‐1 in guiding T cells at the critical point of LN egress when they either exit or return into the LN for further interactions. Abstract The integrin LFA‐1 mediates the adhesion of T cells to lymphatic vessels expressing the LFA‐1 ligand ICAM‐1, prolonging T‐cell retention in lymph nodes to increase their chances of encountering foreign antigens. © European Molecular Biology Organization 2013 |
| abstract_unstemmed |
Abstract Lymphocytes use the integrin leukocyte function‐associated antigen‐1 (LFA‐1) to cross the vasculature into lymph nodes (LNs), but it has been uncertain whether their migration within LN is also LFA‐1 dependent. We show that LFA‐1 mediates prolonged LN residence as LFA‐1−/− CD4 T cells have significantly decreased dwell times compared with LFA‐1+/+ T cells, a distinction lost in hosts lacking the major LFA‐1 ligand ICAM‐1. Intra‐vital two‐photon microscopy revealed that LFA‐1+/+ and LFA‐1−/− T cells reacted differently when probing the ICAM‐1‐expressing lymphatic network. While LFA‐1+/+ T cells returned to the LN parenchyma with greater frequency, LFA‐1−/− T cells egressed promptly. This difference in exit behaviour was a feature of egress through all assessed lymphatic exit sites. We show that use of LFA‐1 as an adhesion receptor amplifies the number of T cells returning to the LN parenchyma that can lead to increased effectiveness of T‐cell response to antigen. Thus, we identify a novel function for LFA‐1 in guiding T cells at the critical point of LN egress when they either exit or return into the LN for further interactions. Abstract The integrin LFA‐1 mediates the adhesion of T cells to lymphatic vessels expressing the LFA‐1 ligand ICAM‐1, prolonging T‐cell retention in lymph nodes to increase their chances of encountering foreign antigens. © European Molecular Biology Organization 2013 |
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6 |
| title_short |
A role for LFA‐1 in delaying T‐lymphocyte egress from lymph nodes |
| url |
https://dx.doi.org/10.1038/emboj.2013.33 |
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| author2 |
Patzak, Irene Jones, Kristian Etemire, Eloho Gunzer, Matthias Hogg, Nancy |
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10.1038/emboj.2013.33 |
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2024-10-22T04:52:18.069Z |
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| score |
7.4003124 |