Repeated antigen challenge modulates expression of follicular dendritic cell (FDC) related molecule in draining lymph nodes

Citation
Y. Ohmori et al., Repeated antigen challenge modulates expression of follicular dendritic cell (FDC) related molecule in draining lymph nodes, ACT HIST CY, 34(4), 2001, pp. 265-273
Citations number
28
Categorie Soggetti
Medical Research Diagnosis & Treatment
Journal title
ACTA HISTOCHEMICA ET CYTOCHEMICA
ISSN journal
00445991 → ACNP
Volume
34
Issue
4
Year of publication
2001
Pages
265 - 273
Database
ISI
SICI code
0044-5991(2001)34:4<265:RACMEO>2.0.ZU;2-P
Abstract
Follicular dendritic cells (FDC) play a pivotal role in the regulation of h umoral immunity, yet the regulatory mechanism of FDC remains largely unknow n. Repeated antigen stimulation of 20 injections of HRP reduces the exchang e of extant for newly arrived antigen on FDCs. This phenomenon might be rel ated to the feedback regulation of FDC under extensive antigen stimuli. In the present study, for better understanding of the phenomenon, we observed the localization of fluorescence-labeled HRP injected after HRP stimuli of up to 40 injections with HRP under a fluorescent microscope, and examined a ntigen exchange on FDCs. Further, we also investigated the expression of ma rker proteins on FDCs in popliteal lymph nodes after repeated injections of HRP into the rat footpad. The decreased accumulation of fluorescent materi al in the germinal center (GMC) of lymph nodes indicated suppressed antigen exchange on FDCs after 20 and 40 antigen stimulations. S-100 protein react ions remained unchanged throughout the study, suggesting that the FDC popul ation was preserved in GMC. On the other hand, EDS positivity peaked and th e reaction area was largest after 20 antigen injections, but weakened after 40 injections. MRC OX-2 reactions in GMC were decreased in 4 of 6 animals given 40 injections, but were positive in other animals. Decreased antigen exchange on FDC and its altered phenotype may play a role in the regulation of FDC function after repeated antigen stimuli.