Infection-Induced Regulation of Natural Killer Cells by Macrophages and Collagen at the Lymph Node Subcapsular Sinus

Infection leads to heightened activation of natural killer (NK) cells, a process that likely involves direct cell-to-cell contact, but how this occurs in vivo is poorly understood. We have used two-photon laser-scanning microscopy in conjunction with Toxoplasma gondii mouse infection models to addre...

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Published inCell reports (Cambridge) Vol. 2; no. 1; pp. 124 - 135
Main Authors Coombes, Janine L., Han, Seong-Ji, van Rooijen, Nico, Raulet, David H., Robey, Ellen A.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 26.07.2012
Elsevier
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Abstract Infection leads to heightened activation of natural killer (NK) cells, a process that likely involves direct cell-to-cell contact, but how this occurs in vivo is poorly understood. We have used two-photon laser-scanning microscopy in conjunction with Toxoplasma gondii mouse infection models to address this question. We found that after infection, NK cells accumulated in the subcapsular region of the lymph node, where they formed low-motility contacts with collagen fibers and CD169+ macrophages. We provide evidence that interactions with collagen regulate NK cell migration, whereas CD169+ macrophages increase the activation state of NK cells. Interestingly, a subset of CD169+ macrophages that coexpress the inflammatory monocyte marker Ly6C had the most potent ability to activate NK cells. Our data reveal pathways through which NK cell migration and function are regulated after infection and identify an important accessory cell population for activation of NK cell responses in lymph nodes. [Display omitted] ► Infection-induced lymph node changes impact natural killer (NK) cell responses ► Following infection, NK cells interact with macrophages near the lymph node capsule ► Inflammatory macrophages activate NK cells ► Interaction with collagen may promote NK cell retention near infection foci The natural killer (NK) cell response to infection is regulated by interactions with cells and components of the extracellular matrix. Robey and colleagues used two-photon laser-scanning microscopy to investigate how these interactions influence NK cell responses to Toxoplasma gondii infection. The authors found that NK cells formed low-motility contacts with collagen fibers and CD169+ macrophages in the subcapsular region of the lymph node, and they show that these interactions regulate NK cell localization and activation, respectively.
AbstractList Infection leads to heightened activation of natural killer (NK) cells, a process that likely involves direct cell-to-cell contact, but how this occurs in vivo is poorly understood. We have used two-photon laser-scanning microscopy in conjunction with Toxoplasma gondii mouse infection models to address this question. We found that after infection, NK cells accumulated in the subcapsular region of the lymph node, where they formed low-motility contacts with collagen fibers and CD169+ macrophages. We provide evidence that interactions with collagen regulate NK cell migration, whereas CD169+ macrophages increase the activation state of NK cells. Interestingly, a subset of CD169+ macrophages that coexpress the inflammatory monocyte marker Ly6C had the most potent ability to activate NK cells. Our data reveal pathways through which NK cell migration and function are regulated after infection and identify an important accessory cell population for activation of NK cell responses in lymph nodes. [Display omitted] ► Infection-induced lymph node changes impact natural killer (NK) cell responses ► Following infection, NK cells interact with macrophages near the lymph node capsule ► Inflammatory macrophages activate NK cells ► Interaction with collagen may promote NK cell retention near infection foci The natural killer (NK) cell response to infection is regulated by interactions with cells and components of the extracellular matrix. Robey and colleagues used two-photon laser-scanning microscopy to investigate how these interactions influence NK cell responses to Toxoplasma gondii infection. The authors found that NK cells formed low-motility contacts with collagen fibers and CD169+ macrophages in the subcapsular region of the lymph node, and they show that these interactions regulate NK cell localization and activation, respectively.
Infection leads to heightened activation of natural killer (NK) cells, a process that likely involves direct cell-to-cell contact, but how this occurs in vivo is poorly understood. We have used two-photon laser-scanning microscopy in conjunction with Toxoplasma gondii mouse infection models to address this question. We found that after infection, NK cells accumulated in the subcapsular region of the lymph node, where they formed low-motility contacts with collagen fibers and CD169(+) macrophages. We provide evidence that interactions with collagen regulate NK cell migration, whereas CD169(+) macrophages increase the activation state of NK cells. Interestingly, a subset of CD169(+) macrophages that coexpress the inflammatory monocyte marker Ly6C had the most potent ability to activate NK cells. Our data reveal pathways through which NK cell migration and function are regulated after infection and identify an important accessory cell population for activation of NK cell responses in lymph nodes.
Infection leads to heightened activation of natural killer (NK) cells, a process that likely involves direct cell-to-cell contact, but how this occurs in vivo is poorly understood. We have used two-photon laser-scanning microscopy in conjunction with Toxoplasma gondii mouse infection models to address this question. We found that after infection, NK cells accumulated in the subcapsular region of the lymph node, where they formed low-motility contacts with collagen fibers and CD169+ macrophages. We provide evidence that interactions with collagen regulate NK cell migration, whereas CD169+ macrophages increase the activation state of NK cells. Interestingly, a subset of CD169+ macrophages that coexpress the inflammatory monocyte marker Ly6C had the most potent ability to activate NK cells. Our data reveal pathways through which NK cell migration and function are regulated after infection and identify an important accessory cell population for activation of NK cell responses in lymph nodes.
Author Coombes, Janine L.
Robey, Ellen A.
van Rooijen, Nico
Han, Seong-Ji
Raulet, David H.
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Snippet Infection leads to heightened activation of natural killer (NK) cells, a process that likely involves direct cell-to-cell contact, but how this occurs in vivo...
Infection leads to heightened activation of natural killer (NK) cells, a process that likely involves direct cell-to-cell contact, but how this occurs in vivo...
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SubjectTerms Accessory cells
Animal models
Animals
Cell activation
Cells, Cultured
Collagen
Collagen - pharmacology
Collagen - physiology
Data processing
Fibers
Infection
Inflammation
Killer Cells, Natural - immunology
Killer Cells, Natural - pathology
Leukocyte migration
Lymph nodes
Lymph Nodes - cytology
Lymph Nodes - drug effects
Lymph Nodes - immunology
Lymph Nodes - pathology
Lymphocyte Activation - drug effects
Lymphocyte Activation - immunology
Macrophages
Macrophages - immunology
Macrophages - pathology
Macrophages - physiology
Mice
Mice, Inbred C57BL
Mice, Inbred CBA
Mice, Transgenic
Microscopy
Models, Biological
Monocytes
Natural killer cells
Sinus
Toxoplasma - growth & development
Toxoplasma - immunology
Toxoplasma gondii
Toxoplasmosis - immunology
Toxoplasmosis - pathology
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Title Infection-Induced Regulation of Natural Killer Cells by Macrophages and Collagen at the Lymph Node Subcapsular Sinus
URI https://dx.doi.org/10.1016/j.celrep.2012.06.001
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