Search

Eine normale histologische Struktur und eine damit verbundene Schutzfunktion von Milzautotransplantaten hangt wesentlich vom Alter des Organismus zum Zeitpunkt der Operation ab. Die im Tierexperiment

Lymphocyte subsets leave the blood and appear in the thoracic duct of normal rats at different rates. The aim of the present study was to investigate their migration pattern through blood, spleen, bone marrow, mesenteric lymph nodes, and Peyer's patches in normal Lewis rats and to study the role of the spleen using splenectomized and spleen-transplanted animals. Fluorescein isothiocyanate (FITC)-labelled thoracic duct lymphocytes (TDL) were injected intravenously into rats and after 15 min, 1, 6, and 24 h the percentages of B, T, T helper (TH) and T-cytotoxic/suppressor (TC/S) lymphocytes in the FITC+ cells were determined in cell suspensions by means of monoclonal antibodies. B and T lymphocytes are preferentially localized in different organs, e.g. B cells in Peyer's patches and T cells in mesenteric lymph nodes. The migration of TH lymphocytes differed from that of TC/S lymphocytes in all the organs investigated. In the late phase after injection the migration of B and TH lymphocytes was influenced by the spleen, since after splenectomy the number of injected B lymphocytes increased and that of TH lymphocytes decreased in all organs investigated except the bone marrow. Splenic autotransplantation could not normalize the disturbed migration.

Immunohistochemical methods are described for the detection and characterization of fluorescein isothiocyanate (FITC)-labelled lymphocytes on cryostat sections using an anti-FITC antibody. As a model, the localization of thoracic duct lymphocytes (TDL) in the rat spleen was examined at three time intervals. The kinetic patterns observed clearly differed between the four splenic compartments examined, namely: the red pulp, the marginal zone, the periarteriolar lymphatic sheath (PALS) and the follicle. Furthermore, the subset composition of the immigrant lymphocytes was determined by two colour immunohistochemical staining, which permitted simultaneous detection of the FITC label and surface markers. The results suggest that this method is a fast, easy and inexpensive approach to studies of lymphocyte migration.