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E. Riboldi, T. Musso, E. Moroni, C. Urbinati, S. Bernasconi, M. Rusnati, L. Adorini, M. Presta, S. Sozzani (2005)
Cutting Edge: Proangiogenic Properties of Alternatively Activated Dendritic Cells1The Journal of Immunology, 175
A. Ruddell, P. Mezquita, Kimberly Brandvold, A. Farr, B. Iritani (2003)
B lymphocyte-specific c-Myc expression stimulates early and functional expansion of the vasculature and lymphatics during lymphomagenesis.The American journal of pathology, 163 6
T. Mempel, S. Henrickson, U. Andrian (2004)
T-cell priming by dendritic cells in lymph nodes occurs in three distinct phasesNature, 427
M. Bajénoff, S. Granjeaud, S. Guerder (2003)
The Strategy of T Cell Antigen-presenting Cell Encounter in Antigen-draining Lymph Nodes Revealed by Imaging of Initial T Cell ActivationThe Journal of Experimental Medicine, 198
Weili Zhao, S. Mourah, N. Mounier, C. Leboeuf, M. Daneshpouy, L. Legrès, V. Meignin, É. Oksenhendler, Christine Maignin, F. Calvo, J. Brière, C. Gisselbrecht, A. Janin (2004)
Vascular endothelial growth factor-A is expressed both on lymphoma cells and endothelial cells in angioimmunoblastic T-cell lymphoma and related to lymphoma progressionLaboratory Investigation, 84
P. Carmeliet (2003)
Angiogenesis in health and diseaseNature Medicine, 9
B. Trowbridge (1978)
Interspecies spleen-myeloma hybrid producing monoclonal antibodies against mouse lymphocyte surface glycoprotein, T200The Journal of Experimental Medicine, 148
T. Curiel, P. Cheng, P. Mottram, Xavier Alvarez, L. Moons, Melina Evdemon-Hogan, Shuang Wei, L. Zou, Ilona Kryczek, G. Hoyle, A. Lackner, P. Carmeliet, W. Zou (2004)
Dendritic Cell Subsets Differentially Regulate Angiogenesis in Human Ovarian CancerCancer Research, 64
Jun-ichiro Nishi, K. Arimura, A. Utsunomiya, S. Yonezawa, K. Kawakami, N. Maeno, O. Ijichi, N. Ikarimoto, Masanori Nakata, I. Kitajima, T. Fukushige, Hideo Takamatsu, K. Miyata, I. Maruyama (1999)
Expression of vascular endothelial growth factor in sera and lymph nodes of the plasma cell type of Castleman's diseaseBritish Journal of Haematology, 104
K. Nishioka, I. Katayama (1978)
Angiogenic activity in culture supernatant of antigen‐stimulated lymph node cellsThe Journal of Pathology, 126
A. Luttun, M. Tjwa, L. Moons, Yan Wu, A. Angelillo-Scherrer, F. Liao, J. Nagy, A. Hooper, J. Priller, Bert Klerck, V. Compernolle, E. Daci, P. Bőhlen, M. Dewerchin, J. Herbert, R. Fava, P. Matthys, G. Carmeliet, D. Collen, H. Dvorak, D. Hicklin, P. Carmeliet (2002)
Revascularization of ischemic tissues by PlGF treatment, and inhibition of tumor angiogenesis, arthritis and atherosclerosis by anti-Flt1Nature Medicine, 8
V. Angeli, F. Ginhoux, Jaime Llodrá, L. Quéméneur, P. Frenette, M. Skobe, R. Jessberger, M. Merad, G. Randolph (2006)
B cell-driven lymphangiogenesis in inflamed lymph nodes enhances dendritic cell mobilization.Immunity, 24 2
M. Lutz, N. Kukutsch, A. Ogilvie, S. Rössner, F. Koch, N. Romani, G. Schuler (1999)
An advanced culture method for generating large quantities of highly pure dendritic cells from mouse bone marrow.Journal of immunological methods, 223 1
K. Soderberg, G. Payne, A. Sato, R. Medzhitov, S. Segal, A. Iwasaki (2005)
Innate control of adaptive immunity via remodeling of lymph node feed arteriole.Proceedings of the National Academy of Sciences of the United States of America, 102 45
P. Streeter, B. Rouse, E. Butcher (1988)
Immunohistologic and functional characterization of a vascular addressin involved in lymphocyte homing into peripheral lymph nodesThe Journal of Cell Biology, 107
S. Hemmerich, A. Bistrup, M. Singer, A. Zante, Jin Lee, D. Tsay, Meredith Peters, Janet Carminati, Thomas Brennan, K. Carver-Moore, Michael Leviten, Maria Fuentes, N. Ruddle, S. Rosen (2001)
Sulfation of L-selectin ligands by an HEV-restricted sulfotransferase regulates lymphocyte homing to lymph nodes.Immunity, 15 2
H. Foss, I. Araújo, G. Demel, Heike Klotzbach, M. Hummel, H. Stein (1997)
Expression of vascular endothelial growth factor in lymphomas and castleman's diseaseThe Journal of Pathology, 183
T. Eubank, Michelle Galloway, Christine Montague, W. Waldman, Clay Marsh (2003)
M-CSF Induces Vascular Endothelial Growth Factor Production and Angiogenic Activity From Human Monocytes 1The Journal of Immunology, 171
J. Fries, A. Williams, R. Atkins, Walter, Newman, M. Lipscomb, T. Collins (1993)
Expression of VCAM-1 and E-selectin in an in vivo model of endothelial activation.The American journal of pathology, 143 3
P. Baluk, T. Tammela, Erin Ator, Natalya Lyubynska, M. Achen, D. Hicklin, M. Jeltsch, T. Petrova, B. Pytowski, S. Stacker, S. Ylä-Herttuala, D. Jackson, K. Alitalo, D. McDonald (2005)
Pathogenesis of persistent lymphatic vessel hyperplasia in chronic airway inflammation.The Journal of clinical investigation, 115 2
J. Banchereau, R. Steinman (1998)
Dendritic cells and the control of immunityNature, 392
R. Burwell (1962)
STUDIES OF THE PRIMARY AND THE SECONDARY IMMUNE RESPONSES OF LYMPH NODES DRAINING HOMOGRAFTS OF FRESH CANCELLOUS BONE (WITH PARTICULAR REFERENCE TO MECHANISMS OF LYMPH NODE REACTIVITY)Annals of the New York Academy of Sciences, 99
L. Fina, H. Molgaard, D. Robertson, Bradley Nj, P. Monaghan, D. Delia, Sutherland Dr, Baker Ma, M. Greaves (1990)
Expression of the CD34 gene in vascular endothelial cells.Blood, 75 12
Suneale Banerji, J. Ni, Shu-Xia Wang, S. Clasper, Jeffrey Su, R. Tammi, Margaret Jones, D. Jackson (1999)
LYVE-1, a New Homologue of the CD44 Glycoprotein, Is a Lymph-specific Receptor for HyaluronanThe Journal of Cell Biology, 144
Li Yang, L. Debusk, Koari Fukuda, B. Fingleton, B. Green-Jarvis, Y. Shyr, L. Matrisian, D. Carbone, P. Lin (2004)
Expansion of myeloid immune suppressor Gr+CD11b+ cells in tumor-bearing host directly promotes tumor angiogenesis.Cancer cell, 6 4
S. Hirakawa, S. Kodama, R. Kunstfeld, K. Kajiya, L. Brown, M. Detmar (2005)
VEGF-A induces tumor and sentinel lymph node lymphangiogenesis and promotes lymphatic metastasisThe Journal of Experimental Medicine, 201
P. Mombaerts, J. Iacomini, R. Johnson, K. Herrup, S. Tonegawa, V. Papaioannou (1992)
RAG-1-deficient mice have no mature B and T lymphocytesCell, 68
T. Asahara, T. Murohara, A. Sullivan, Marcy Silver, R. Zee, Tong Li, B. Witzenbichler, G. Schatteman, J. Isner (1997)
Isolation of Putative Progenitor Endothelial Cells for AngiogenesisScience, 275
D. Steeber, C. Erickson, K. Hodde, R. Albrecht (1987)
Vascular changes in popliteal lymph nodes due to antigen challenge in normal and lethally irradiated mice.Scanning microscopy, 1 2
M. Gimbrone, S. Leapman, R. Cotran, J. Folkman (1972)
TUMOR DORMANCY IN VIVO BY PREVENTION OF NEOVASCULARIZATIONThe Journal of Experimental Medicine, 136
J. Hay, B. Hobbs (1977)
The flow of blood to lymph nodes and its relation to lymphocyte traffic and the immune responseThe Journal of Experimental Medicine, 145
A. Martín-Fontecha, L. Thomsen, S. Brett, C. Gerard, M. Lipp, A. Lanzavecchia, F. Sallusto (2004)
Induced recruitment of NK cells to lymph nodes provides IFN-gamma for T(H)1 priming.Nature immunology, 5 12
M. Grunewald, I. Avraham, Y. Dor, E. Bachar-Lustig, A. Itin, S. Yung, S. Chimenti, Limor Landsman, R. Abramovitch, E. Keshet (2006)
VEGF-Induced Adult Neovascularization: Recruitment, Retention, and Role of Accessory CellsCell, 124
N. Ferrara, K. Carver-Moore, Helen Chen, M. Dowd, Lucy Lu, K. O'shea, L. Powell-Braxton, K. Hillan, M. Moore (1996)
Heterozygous embryonic lethality induced by targeted inactivation of the VEGF geneNature, 380
W. Gallatin, I. Weissman, E. Butcher (1983)
A cell-surface molecule involved in organ-specific homing of lymphocytesNature, 304
J. Conejo-Garcia, F. Benencia, M. Courreges, E. Kang, A. Mohamed-Hadley, R. Buckanovich, David Holtz, Ann Jenkins, Hana Na, Lin Zhang, D. Wagner, D. Katsaros, Richard Caroll, G. Coukos (2004)
Tumor-infiltrating dendritic cell precursors recruited by a β-defensin contribute to vasculogenesis under the influence of Vegf-ANature Medicine, 10
S. Luther, A. Gulbranson‐Judge, H. Acha-Orbea, I. Maclennan (1997)
Viral Superantigen Drives Extrafollicular and Follicular B Cell Differentiation Leading to Virus-specific Antibody ProductionThe Journal of Experimental Medicine, 185
P. Herman, I. Yamamoto, H. Mellins (1972)
BLOOD MICROCIRCULATION IN THE LYMPH NODE DURING THE PRIMARY IMMUNE RESPONSEThe Journal of Experimental Medicine, 136
Srully Blotnick, G. Peoples, Michael Freeman, Timothy Eberlein, Michael Klagsbrun (1994)
T lymphocytes synthesize and export heparin-binding epidermal growth factor-like growth factor and basic fibroblast growth factor, mitogens for vascular cells and fibroblasts: differential production and release by CD4+ and CD8+ T cells.Proceedings of the National Academy of Sciences of the United States of America, 91
P. Carmeliet, Valérie Ferreira, G. Breier, S. Pollefeyt, L. Kieckens, M. Gertsenstein, M. Fahrig, A. Vandenhoeck, K. Harpal, Carmen Eberhardt, C. Declercq, J. Pawling, L. Moons, D. Collen, W. Risau, A. Nagy (1996)
Abnormal blood vessel development and lethality in embryos lacking a single VEGF alleleNature, 380
J. Conejo-Garcia, R. Buckanovich, F. Benencia, M. Courreges, S. Rubin, R. Carroll, G. Coukos (2005)
Vascular leukocytes contribute to tumor vascularization.Blood, 105 2
M. Lampugnani, M. Resnati, M. Raiteri, R. Pigott, A. Pisacane, G. Houen, L. Ruco, E. Dejana (1992)
A novel endothelial-specific membrane protein is a marker of cell-cell contactsThe Journal of Cell Biology, 118
Bert Oosthuyse, L. Moons, E. Storkebaum, H. Beck, D. Nuyens, K. Brusselmans, J. Dorpe, P. Hellings, M. Gorselink, S. Heymans, G. Theilmeier, M. Dewerchin, V. Laudenbach, P. Vermylen, H. Raat, T. Acker, V. Vleminckx, L. Bosch, N. Cashman, H. Fujisawa, M. Drost, R. Sciot, F. Bruyninckx, D. Hicklin, C. Ince, P. Gressens, F. Lupu, K. Plate, W. Robberecht, J. Herbert, D. Collen, P. Carmeliet (2001)
Deletion of the hypoxia-response element in the vascular endothelial growth factor promoter causes motor neuron degenerationNature Genetics, 28
Minghui Zhang, Hua Tang, Zhenhong Guo, Huazhang An, Xuejun Zhu, Wengang Song, Jun Guo, Xin Huang, Taoyong Chen, Jianli Wang, Xuetao Cao (2004)
Splenic stroma drives mature dendritic cells to differentiate into regulatory dendritic cellsNature Immunology, 5
F. Mor, F. Quintana, I. Cohen (2004)
Angiogenesis-Inflammation Cross-Talk: Vascular Endothelial Growth Factor Is Secreted by Activated T Cells and Induces Th1 PolarizationThe Journal of Immunology, 172
P. Newman, M. Berndt, Jack Gorski, G. White, S. Lyman, C. Paddock, W. Muller (1990)
PECAM-1 (CD31) cloning and relation to adhesion molecules of the immunoglobulin gene superfamily.Science, 247 4947
P. Scapini, M. Morini, C. Tecchio, S. Minghelli, E. Carlo, E. Tanghetti, A. Albini, C. Lowell, G. Berton, D. Noonan, M. Cassatella (2004)
CXCL1/Macrophage Inflammatory Protein-2-Induced Angiogenesis In Vivo Is Mediated by Neutrophil-Derived Vascular Endothelial Growth Factor-A1The Journal of Immunology, 172
R. Palframan, Steffen Jung, G. Cheng, W. Weninger, Yi Luo, M. Dorf, D. Littman, B. Rollins, H. Zweerink, A. Rot, U. Andrian (2001)
Inflammatory Chemokine Transport and Presentation in HEVThe Journal of Experimental Medicine, 194
H. Hashizume, P. Baluk, S. Morikawa, J. Mclean, G. Thurston, S. Roberge, R. Jain, D. McDonald (2000)
Openings between defective endothelial cells explain tumor vessel leakiness.The American journal of pathology, 156 4
M. Pliskin, S. Ginsberg, N. Carp (1980)
Induction of neovascularization by mitogen-activated spleen cells and their supernatants.Transplantation, 29 3
M. Bandt, M. Mahdi, V. Ollivier, M. Grossin, M. Dupuis, M. Gaudry, P. Bőhlen, K. Lipson, A. Rice, Yan Wu, M. Gougerot-Pocidalo, C. Pasquier (2003)
Blockade of Vascular Endothelial Growth Factor Receptor I (VEGF-RI), but not VEGF-RII, Suppresses Joint Destruction in the K/BxN Model of Rheumatoid Arthritis 1The Journal of Immunology, 171
Cornelia Berlin-Rufenach, F. Otto, M. Mathies, J. Westermann, M. Owen, A. Hamann, N. Hogg (1999)
Lymphocyte Migration in Lymphocyte Function-associated Antigen (LFA)-1–deficient MiceThe Journal of Experimental Medicine, 189
B. Osogoe, FC Courtice (1968)
The effects of occlusion of the blood supply to the popliteal lymph node of the rabbit on the cell and protein content of the lymph and on the histology of the node.The Australian journal of experimental biology and medical science, 46 5
N. Anderson, A. Anderson, R. Wyllie (1975)
Microvascular changes in lymph nodes draining skin allografts.The American journal of pathology, 81 1
N. Ferrara, Helen Chen, T. Davis-Smyth, H. Gerber, Thuy-Nhung Nguyen, D. Peers, V. Chisholm, K. Hillan, R. Schwall (1998)
Vascular endothelial growth factor is essential for corpus luteum angiogenesisNature Medicine, 4
B. Rollins, T. Yoshimura, J. Edward, Leonard, Jordan Pobert (1990)
Cytokine-activated human endothelial cells synthesize and secrete a monocyte chemoattractant, MCP-1/JE.The American journal of pathology, 136 6
M. Arbonés, D. Ord, K. Ley, H. Ratech, Catherine Maynard-Curry, G. Otten, D. Capon, Thomas Teddert (1994)
Lymphocyte homing and leukocyte rolling and migration are impaired in L-selectin-deficient mice.Immunity, 1 4
Michele Palma, M. Venneri, R. Galli, Lucia Sergi, L. Politi, M. Sampaolesi, L. Naldini (2005)
Tie2 identifies a hematopoietic lineage of proangiogenic monocytes required for tumor vessel formation and a mesenchymal population of pericyte progenitors.Cancer cell, 8 3
A. Martín-Fontecha, S. Sebastiani, U. Höpken, M. Uguccioni, M. Lipp, A. Lanzavecchia, F. Sallusto (2003)
Regulation of Dendritic Cell Migration to the Draining Lymph NodeThe Journal of Experimental Medicine, 198
Steffen Jung, D. Unutmaz, P. Wong, G. Sano, K. Santos, T. Sparwasser, Shengjia Wu, Srilatha Vuthoori, K. Ko, F. Zavala, E. Pamer, D. Littman, R. Lang (2002)
In vivo depletion of CD11c+ dendritic cells abrogates priming of CD8+ T cells by exogenous cell-associated antigens.Immunity, 17 2
U. Andrian, T. Mempel (2003)
Homing and cellular traffic in lymph nodesNature Reviews Immunology, 3
Lymph nodes grow rapidly and robustly at the initiation of an immune response, and this growth is accompanied by growth of the blood vessels. Although the vessels are critical for supplying nutrients and for controlling cell trafficking, the regulation of lymph node vascular growth is not well understood. We show that lymph node endothelial cells begin to proliferate within 2 d of immunization and undergo a corresponding expansion in cell numbers. Endothelial cell proliferation is dependent on CD11c+ dendritic cells (DCs), and the subcutaneous injection of DCs is sufficient to trigger endothelial cell proliferation and growth. Lymph node endothelial cell proliferation is dependent on vascular endothelial growth factor (VEGF), and DCs are associated with increased lymph node VEGF levels. DC-induced endothelial cell proliferation and increased VEGF levels are mediated by DC-induced recruitment of blood-borne cells. Vascular growth in the draining lymph node includes the growth of high endothelial venule endothelial cells and is functionally associated with increased cell entry into the lymph node. Collectively, our results suggest a scenario whereby endothelial cell expansion in the draining lymph node is induced by DCs as part of a program that optimizes the microenvironment for the ensuing immune response.
The Journal of Experimental Medicine – Pubmed Central
Published: Aug 7, 2006
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