MHC-LINKED COLONIZATION OF THE THYMUS AND THYMOCYTE DEVELOPMENT - EFFECTS OF MATURE T-LYMPHOCYTES

Citation
A. Sharp et al., MHC-LINKED COLONIZATION OF THE THYMUS AND THYMOCYTE DEVELOPMENT - EFFECTS OF MATURE T-LYMPHOCYTES, International archives of allergy and immunology, 106(1), 1995, pp. 13-19
Citations number
29
Categorie Soggetti
Allergy,Immunology
ISSN journal
10182438
Volume
106
Issue
1
Year of publication
1995
Pages
13 - 19
Database
ISI
SICI code
1018-2438(1995)106:1<13:MCOTTA>2.0.ZU;2-V
Abstract
Effects of mature T lymphocytes on thymic colonization by lymphohemopo ietic cells were investigated in an in vitro experimental model, using a variety of experimental strategies. Lymphoid-depleted fetal thymus (FT) explants (C57BL/Ka, Thy1.1, H-2(b)) were incubated with bone mall ow (BM) cells from syngeneic (C57BL/Ka; SBM) and allogeneic (BALB/c, T hy1.2, H-2(d); ABM) donors. Cocultures of FT with SBM and ABM, deplete d of Thy1+ or of CD3+ cells, resulted in equal proportions of lymphocy tes from both BM donors. When peripheral blood lymphocytes (PBL) from synegenic or semi-allogeneic donors (F1[C57BL/KaxC57BL/6J], Thy1.1/Thy 1.2); or F1[C57BL/KaxBALB/c], Thy1.1/Thy1.2, respectively) were added to these cultures, the total lymphocyte count per thymic lobe decrease d and a developmental preference of the SBM-derived cells, as compared to the ABM-derived cells, was noted. Cells of the PBL types were also observed in the cultures. Cocultures of FT with ABM and PBL showed re duced proportions of ABM-derived cells and occurrence of cells of the PBL type. Finally, FT explants partially depleted of lymphocytes by ir radiation (6 Gy), were cocultured with PBL from either syngeneic or al logeneic donors. In the presence of syngeneic PBL, the total number of cells and the proportion of double-positive (CD4+CD8+) T cells were s imilar to those in the FT cultured by itself, whereas in the presence of allogeneic PBL these values were reduced. The study suggests that m ature T lymphocytes may play a role in the developmental processes in the thymus, and points to MHC-linked selective effects.