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Lymphatic Endothelium Forms Integrin-Engaging 3D Structures during DC Transit across Inflamed Lymphatic Vessels
by
Ochoa, Carmen
, Alfaro, Carlos
, Azpilikueta, Arantza
, Rouzaut, Ana
, Aubá, Cristina
, Rodrigues, Magda
, Teijeira, Álvaro
, Valitutti, Salvatore
, Melero, Ignacio
, Peláez, Rafael
, Marré, Diego
, Garasa, Saray
in
Animals
/ Cell Adhesion - physiology
/ Cell Communication - physiology
/ Cell Differentiation - physiology
/ Cell Movement - physiology
/ Dendritic Cells - cytology
/ Dendritic Cells - metabolism
/ Dermatitis - metabolism
/ Dermatitis - pathology
/ Dermis - cytology
/ Endothelial Cells - cytology
/ Endothelial Cells - drug effects
/ Endothelial Cells - metabolism
/ Humans
/ Imaging, Three-Dimensional - methods
/ Integrins - metabolism
/ Intercellular Adhesion Molecule-1 - metabolism
/ Lymphadenitis - metabolism
/ Lymphadenitis - pathology
/ Lymphatic Vessels - cytology
/ Lymphatic Vessels - physiology
/ Lymphocyte Function-Associated Antigen-1 - metabolism
/ Male
/ Mice
/ Mice, Inbred C57BL
/ Microvilli - physiology
/ Tumor Necrosis Factor-alpha - pharmacology
2013
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Lymphatic Endothelium Forms Integrin-Engaging 3D Structures during DC Transit across Inflamed Lymphatic Vessels
by
Ochoa, Carmen
, Alfaro, Carlos
, Azpilikueta, Arantza
, Rouzaut, Ana
, Aubá, Cristina
, Rodrigues, Magda
, Teijeira, Álvaro
, Valitutti, Salvatore
, Melero, Ignacio
, Peláez, Rafael
, Marré, Diego
, Garasa, Saray
in
Animals
/ Cell Adhesion - physiology
/ Cell Communication - physiology
/ Cell Differentiation - physiology
/ Cell Movement - physiology
/ Dendritic Cells - cytology
/ Dendritic Cells - metabolism
/ Dermatitis - metabolism
/ Dermatitis - pathology
/ Dermis - cytology
/ Endothelial Cells - cytology
/ Endothelial Cells - drug effects
/ Endothelial Cells - metabolism
/ Humans
/ Imaging, Three-Dimensional - methods
/ Integrins - metabolism
/ Intercellular Adhesion Molecule-1 - metabolism
/ Lymphadenitis - metabolism
/ Lymphadenitis - pathology
/ Lymphatic Vessels - cytology
/ Lymphatic Vessels - physiology
/ Lymphocyte Function-Associated Antigen-1 - metabolism
/ Male
/ Mice
/ Mice, Inbred C57BL
/ Microvilli - physiology
/ Tumor Necrosis Factor-alpha - pharmacology
2013
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Lymphatic Endothelium Forms Integrin-Engaging 3D Structures during DC Transit across Inflamed Lymphatic Vessels
by
Ochoa, Carmen
, Alfaro, Carlos
, Azpilikueta, Arantza
, Rouzaut, Ana
, Aubá, Cristina
, Rodrigues, Magda
, Teijeira, Álvaro
, Valitutti, Salvatore
, Melero, Ignacio
, Peláez, Rafael
, Marré, Diego
, Garasa, Saray
in
Animals
/ Cell Adhesion - physiology
/ Cell Communication - physiology
/ Cell Differentiation - physiology
/ Cell Movement - physiology
/ Dendritic Cells - cytology
/ Dendritic Cells - metabolism
/ Dermatitis - metabolism
/ Dermatitis - pathology
/ Dermis - cytology
/ Endothelial Cells - cytology
/ Endothelial Cells - drug effects
/ Endothelial Cells - metabolism
/ Humans
/ Imaging, Three-Dimensional - methods
/ Integrins - metabolism
/ Intercellular Adhesion Molecule-1 - metabolism
/ Lymphadenitis - metabolism
/ Lymphadenitis - pathology
/ Lymphatic Vessels - cytology
/ Lymphatic Vessels - physiology
/ Lymphocyte Function-Associated Antigen-1 - metabolism
/ Male
/ Mice
/ Mice, Inbred C57BL
/ Microvilli - physiology
/ Tumor Necrosis Factor-alpha - pharmacology
2013
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Lymphatic Endothelium Forms Integrin-Engaging 3D Structures during DC Transit across Inflamed Lymphatic Vessels
Journal Article
Lymphatic Endothelium Forms Integrin-Engaging 3D Structures during DC Transit across Inflamed Lymphatic Vessels
2013
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Overview
Dendritic cell (DC) transmigration across the lymphatic endothelium is critical for the initiation and sustenance of immune responses. Under noninflammatory conditions, DC transit across the lymphatic endothelial cell (LEC) has been shown to be integrin independent. In contrast, there is increasing evidence for the participation of integrins and their ligands in DC transit across lymphatic endothelium under inflammation. In this sense, we describe the formation of ICAM-1 (CD54)-enriched three-dimensional structures on LEC/DC contacts, as these DCs adhere to inflamed skin lymphatic vessels and transmigrate into them. In vitro imaging revealed that under inflammation ICAM-1 accumulated on microvilli projections surrounding 60% of adhered DCs. In contrast, these structures were scarcely formed in noninflammatory conditions. Furthermore, ICAM-1-enriched microvilli were important in promoting DC transendothelial migration and DC crawling over the LEC surface. Microvilli formation was dependent on the presence of β-integrins on the DC side and on integrin conformational affinity to ligand. Finally, we observed that LEC microvilli structures appeared in close vicinity of CCL21 depots and that their assembly was partially inhibited by CCL21-neutralizing antibodies. Therefore, under inflammatory conditions, integrin ligands form three-dimensional membrane projections around DCs. These structures offer docking sites for DC transit from the tissue toward the lymphatic vessel lumen.
Publisher
Elsevier Inc,Elsevier Limited
Subject
/ Cell Communication - physiology
/ Cell Differentiation - physiology
/ Dendritic Cells - metabolism
/ Endothelial Cells - cytology
/ Endothelial Cells - drug effects
/ Endothelial Cells - metabolism
/ Humans
/ Imaging, Three-Dimensional - methods
/ Intercellular Adhesion Molecule-1 - metabolism
/ Lymphatic Vessels - cytology
/ Lymphatic Vessels - physiology
/ Lymphocyte Function-Associated Antigen-1 - metabolism
/ Male
/ Mice
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