Reference : Precise localization of antigens on follicular dendritic cells.
Scientific journals : Article
Life sciences : Anatomy (cytology, histology, embryology...) & physiology
http://hdl.handle.net/2268/23228
Precise localization of antigens on follicular dendritic cells.
English
Radoux, D. [ > > ]
Heinen, Ernst mailto [Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Histologie humaine >]
Kinet-Denoel, C. [> > > >]
Tihange, E. [> > > >]
Simar, L. [> > > >]
1984
Cell & Tissue Research
Springer Science & Business Media B.V.
235
2
267-74
Yes (verified by ORBi)
International
0302-766X
1432-0878
New York
NY
[en] Animals ; Antigens, Surface/analysis ; Female ; Ferritins ; Gold ; Lymph Nodes/immunology/ultrastructure ; Lymphocytes/immunology/ultrastructure ; Mice ; Mice, Inbred C57BL ; Microscopy, Electron ; Serum Albumin
[en] Horse-spleen ferritin or bovine serum albumin conjugated to colloidal gold (BSA-gold) were injected subcutaneously in preimmunized mice. In draining lymph nodes both antigens were located in macrophages or between the cytoplasmic processes of follicular dendritic cells (FDC). Some of the antigens remained trapped on FDC until day 31 after injection. Simultaneous injection of both antigens showed that they were located between the infoldings of the same FDC. These cells are thus able to retain at least two different antigens on their surface. The peculiar arrangement of ferritin between the cytoplasmic infoldings suggests that this antigen is fixed on both cell membranes by specific antibodies. The trapped immune complexes could thus stabilize the FDC membrane system. The antigen retention requires the presence of specific antibodies since BSA-gold or ferritin injected without preimmunization were not found between FDC processes. Nonantigenic materials, such as colloidal gold or carbon particles, are not trapped by FDC, except when injected in large amounts. The antigens were trapped on the surface of FDC, however unfrequently in close contact with lymphocytes. FDC might protect lymphocytes against an excess of immune complexes and act as regulators of contacts between lymphocytes and immune complexes.
http://hdl.handle.net/2268/23228
10.1007/BF00217850

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