PERITONEAL-MACROPHAGES PLAY AN IMPORTANT ROLE IN ELIMINATING HUMAN-CELLS FROM SEVERE COMBINED IMMUNODEFICIENT MICE TRANSPLANTED WITH HUMAN PERIPHERAL-BLOOD LYMPHOCYTES

Citation
S. Shibata et al., PERITONEAL-MACROPHAGES PLAY AN IMPORTANT ROLE IN ELIMINATING HUMAN-CELLS FROM SEVERE COMBINED IMMUNODEFICIENT MICE TRANSPLANTED WITH HUMAN PERIPHERAL-BLOOD LYMPHOCYTES, Immunology, 93(4), 1998, pp. 524-532
Citations number
31
Categorie Soggetti
Immunology
Journal title
ISSN journal
00192805
Volume
93
Issue
4
Year of publication
1998
Pages
524 - 532
Database
ISI
SICI code
0019-2805(1998)93:4<524:PPAIRI>2.0.ZU;2-X
Abstract
To elucidate che mechanism of human cell elimination from severe combi ned immunodeficient (SCID) mice transplanted with human peripheral blo od lymphocytes (hu-PBL-SCID mice), we explored the immunocytes in the peritoneal cavity in SCID mice where human PBL were transferred. When the phenotype of peritoneal exudate cells (PEC) was compared by flow c ytometry among three congenic strains of SCID mice that differ in thei r acceptability for human PBL, the PEC in NOD-scid mice, which exhibit the highest acceptability, contained the smallest number of F4/80(lot -)Mac-1(+)-activated macrophages. Moreover, the proportions of natural killer cells in PEC of the three strains of SCID mice were not always correlated with the acceptability. These findings suggest the possibi lity that peritoneal macrophages eliminate human cells in hu-PBL-SCID mice. To verify this hypothesis, we evaluated the engraftment of human PBL into SCID mice that were treated with liposome-encapsulated dichl oromethylene diphosphonate, which selectively depletes macrophages by inducing apoptosis, or S-aminoguanidine hemisulphate salt, an inhibito r of inducible nitric oxide synthase of macrophages. As a result, both of these regimens improved engraftment of human PBL: indicating that peritoneal macrophages take part in human cell elimination in the peri toneal cavity of bu-PBL-SCID mice and that it is mediated, at least in part, by direct macrophage cytotoxicity utilizing nitric oxide.