Abstract
Hair growth abnormalities in mice usually are accompanied by histologic abnormalities as well. Recently, however, we reported a mouse model in which an arrest of the hair cycle and diffuse shedding of the hair without pathologic features induced alopecia in interferon-γ -/- (IFN-γ -/-) C57BL/6 (B6) mice. Here, we explored the cellular origin of IFN-γ. When bone marrow from IFN-γ -/- B6 mice was transplanted into lethally irradiated IFN-γ +/+ B6 mice, the level of IFN-γ mRNA expression in the skin or peripheral blood mononuclear cells (PBMCs) of recipient mouse was markedly reduced, suggesting that IFN-γ is normally produced by bone marrow-derived cells. Although severe combined immunodeficiency (SCID) mice lack mature T cells and B cells, IFN-γ-dependent hair regrowth was induced in SCID mice by depilation, which caused alopecia in IFN-γ -/- B6 mice. Consistently, IFN-γ mRNA expression in the skin or PBMC from SCID mice was comparable to that from their genetic counterpart (BALB/c mice), suggesting IFN-γ production by non-T cells. RT-PCR analyses after separation of PBMC from SCID mice into eight fractions by a cell sorter revealed that Mac-1+ cells were the major origin of IFN-γ.
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