The role of the DAP12 signal in mouse myeloid differentiation

被引:36
作者
Aoki, N
Kimura, S
Takiyama, Y
Atsuta, Y
Abe, A
Sato, K
Katagiri, M
机构
[1] Asahikawa Med Coll, Dept Pathol, Asahikawa, Hokkaido 0788510, Japan
[2] Asahikawa Med Coll, Sch Nursing, Asahikawa, Hokkaido 0788510, Japan
关键词
D O I
10.4049/jimmunol.165.7.3790
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
DAP12. is a recently cloned, immunoreceptor tyrosine-based activation motif-bearing transmembrane adapter molecule that is associated with the NK-activating receptors, Previous reports showed that the DAP12 message could be detected not only in NK cells but also in granulocytes, monocytes, dendritic cells, and macrophages, In this study we found a significant level of DAP12 protein expression in macrophage-related cell lines and organs. Additionally, we observed increased expression of DAP12, after LPS-induced differentiation of M1 cells into macrophages, To examine the role of DAP12 in the myeloid cell lineage, we established M1 FLAG-DAP12 transfectants (FDAP-M1) and demonstrated the marked;morphological changes in FDAP-M1 cells caused by signaling through DAP12 Cell surface phenotypic analysis showed up-regulation of macrophage markers CD11b, 2,4G2, and adhesion molecule B7-2, Additionally, after stimulation through DAP12, phosphorylated FLAG -DAP12 could be immunoprecipitated using anti-phosphotyrosine mAbs, Collectively, these findings indicate that direct DAP12 signaling has an important role in macrophage differentiation.
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收藏
页码:3790 / 3796
页数:7
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