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Graft‐versus‐host‐disease‐associated donor cell engraftment in an F 1 hybrid model is dependent upon the Fas pathway
Author(s) -
Iwasaki T.,
Hamano T.,
Saheki K.,
Kuroiwa T.,
Kataoka Y.,
Takemoto Y.,
Ogata A.,
Fujimoto J.,
Kakishita E.
Publication year - 2000
Publication title -
immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.297
H-Index - 133
eISSN - 1365-2567
pISSN - 0019-2805
DOI - 10.1046/j.1365-2567.2000.00919.x
Subject(s) - fas ligand , haematopoiesis , apoptosis , spleen , immunology , biology , bone marrow , fas receptor , tumor necrosis factor alpha , interferon , progenitor cell , graft versus host disease , stem cell , microbiology and biotechnology , programmed cell death , genetics
Summary The graft‐versus‐host disease (GVHD) generated in BDF 1 mice by the injection of spleen cells from the C57BL/6 parental strain induces a direct cell‐mediated attack on host lymphohaematopoietic populations, resulting in the reconstitution of the host with donor cells. We examined Fas–Fas ligand (FasL) interactions in donor and host haematopoietic cells over a prolonged period of parental‐induced GVHD. Fas expression on bone marrow cells of both donor and host origin increased at 2 weeks. Host cell incubation with anti‐Fas antibody induced apoptosis, and the number of haematopoietic progenitor cells decreased. Fas‐induced apoptosis by the repopulating donor cells, however, did not increase until 12 weeks, when more than 90% of the cells were donor cells. The expression of various cytokines, such as interferon‐γ (IFN‐γ) and tumour necrosis factor‐α (TNF‐α), and FasL gene expression in the bone marrow increased concomitantly. To examine directly whether FasL has a major role in the development of donor cell engraftment, FasL‐deficient ( gld ) mice were used as donors. Injection of B6/ gld spleen cells induced significantly less host lymphohaematopoietic depletion, resulting in a failure of donor cell engraftment. Furthermore, injection of IFN‐γ gene knockout ( gko ) B6 spleen cells failed to augment Fas and FasL expression in recipient mice, resulting in a failure of donor cell engraftment. This suggests that the induction of apoptosis by Fas–FasL interactions in host cells may contribute to a reconstitution of the host with donor cells and that donor‐derived IFN‐γ plays a significant role for Fas–FasL interactions in host cells during parental‐induced GVHD.