APCs in the anterior uveal tract do not migrate to draining lymph nodes

被引:34
作者
Dullforce, PA
Garman, KL
Seitz, GW
Fleischmann, RJ
Crespo, SM
Planck, SR
Parker, DC
Rosenbaum, JT
机构
[1] Oregon Hlth & Sci Univ, Casey Eye Inst, Dept Ophthalmol, Portland, OR 97239 USA
[2] Oregon Hlth & Sci Univ, Casey Eye Inst, Dept Cell & Dev Biol, Portland, OR 97239 USA
[3] Oregon Hlth & Sci Univ, Casey Eye Inst, Dept Med, Portland, OR 97239 USA
[4] Oregon Hlth & Sci Univ, Casey Eye Inst, Dept Mol Biol & Immunol, Portland, OR 97239 USA
关键词
D O I
10.4049/jimmunol.172.11.6701
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The migration of APCs from sites of infection and their maturation are critical elements in the generation of immune responses. However, the paths by which intraocular Ags migrate to draining lymph nodes are not known because the eye has limited lymphatic vessels. To date, only dendritic cells from the cornea and conjunctiva have been shown to emigrate. We demonstrate that phagocytic APCs in the anterior uveal tissues of the murine eye that ingest fluorescent latex beads do not migrate to regional lymph nodes. The beads are ingested in the uveal tract by cells expressing MHC class II, CD11c, or F4/80. Using intravital time-lapse videomicroscopy to monitor iris APC migration after anterior chamber injection of fluorescent Ag, fluorescently labeled APCs fail to move at multiple observation times, even in the presence of Ag and LPS. Whereas an as yet unidentified ocular nonphagocytic APC subset might migrate from the anterior uveal tissues, it is more probable that immune responses in the draining lymph nodes are engendered by soluble Ag escaping the eye through interstitial spaces. The inability of anterior uveal tissue APCs to migrate to lymph nodes may contribute to deviant immune responses that dominate after Ags are introduced into the anterior chamber.
引用
收藏
页码:6701 / 6708
页数:8
相关论文
共 56 条
[1]   Regulation of T-cell responses by CNS antigen-presenting cells: different roles for microglia and astrocytes [J].
Aloisi, F ;
Ria, F ;
Adorini, L .
IMMUNOLOGY TODAY, 2000, 21 (03) :141-147
[2]   Mouse type IIFN-producing cells are immature APCs with plasmacytoid morphology [J].
Asselin-Paturel, C ;
Boonstra, A ;
Dalod, M ;
Durand, I ;
Yessaad, N ;
Dezutter-Dambuyant, C ;
Vicari, A ;
O'Garra, A ;
Biron, C ;
Brière, F ;
Trinchieri, G .
NATURE IMMUNOLOGY, 2001, 2 (12) :1144-1150
[3]   The strategy of T cell antigen-presenting cell encounter in antigen-draining lymph nodes revealed by imaging of initial T cell activation [J].
Bajénoff, M ;
Granjeaud, S ;
Guerder, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 198 (05) :715-724
[4]   Digital video-imaging of leukocyte migration in the iris: intravital microscopy in a physiological model during the onset of endotoxin-induced uveitis [J].
Becker, MD ;
Nobiling, R ;
Planck, SR ;
Rosenbaum, JT .
JOURNAL OF IMMUNOLOGICAL METHODS, 2000, 240 (1-2) :23-37
[5]  
Becker MD, 2000, INVEST OPHTH VIS SCI, V41, P1812
[6]   Immunohistology of antigen-presenting cells in vivo: A novel method for serial observation of fluorescently labeled cells [J].
Becker, MD ;
Planck, SR ;
Crespo, S ;
Garman, K ;
Fleischman, RJ ;
Dullforce, P ;
Seitz, GW ;
Martin, TM ;
Parker, DC ;
Rosenbaum, JT .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2003, 44 (05) :2004-2009
[9]   The distribution of antigen in lymphoid tissues following its injection into the anterior chamber of the rat eye [J].
Camelo, S ;
Shanley, A ;
Voon, ASP ;
McMenamin, PG .
JOURNAL OF IMMUNOLOGY, 2004, 172 (09) :5388-5395
[10]  
Chen L, 2002, CLIN IMMUNOL, V103, pS16