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Loss of a single Zn finger, but not that of two Zn fingers, of GATA3 drives skin inflammation
被引:0
|作者:
Iguchi, Tomohiro
[1
]
Toma-Hirano, Makiko
[2
]
Takanashi, Masakatsu
[3
]
Masai, Hisao
[1
]
Miyatake, Shoichiro
[1
,4
]
机构:
[1] Tokyo Metropolitan Inst Med Sci, Dept Basic Med Sci, Genome Dynam Project, Tokyo, Japan
[2] Teikyo Univ, Fac Med, Dept Otolaryngol, Tokyo, Japan
[3] Azabu Univ, Grad Sch Environm Hlth Sci, Dept Pathol, Sagamihara, Japan
[4] Azabu Univ, Grad Sch Environm Hlth Sci, Dept Immunol, Sagamihara, Japan
基金:
日本学术振兴会;
关键词:
dermatitis;
GATA3;
LAG3;
MHC class II;
S100;
proteins;
Zn finger;
TRANSCRIPTION FACTOR GATA-3;
T-CELLS;
ACTIVATION;
EXPRESSION;
PROTEOMICS;
BINDING;
PROTEIN;
D O I:
10.1111/gtc.13171
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Transcription factor GATA3 is essential for the developmental processes of T cells. Recently, the silencer of a cytokine IFN gamma gene was identified, the inhibitory activity of which requires GATA3. GATA3 has 2 Zn fingers and the commonly used GATA3 deficient mice lack both fingers (D2). We have established a mouse line that lacks only one Zn finger close to the C terminus (D1). The D1 mice line developed dermatitis, which was not observed in D2 mice. The expression of S100a8/S100a9 was elevated in D1 to a level higher than in D2, suggesting their roles in dermatitis development. CD8 T cells of both D1 and D2 lines expressed inhibitory receptors associated with the exhausted state. In the absence of MHC class II, the skin inflammation was exacerbated in both lines. The gene expression pattern of CD8 T cells became similar to that of effector T cells. Blocking Ab against LAG3 upregulated the expression of the effector molecules of T cells. These results suggest that the disfunction of GATA3 can lead to the spontaneous activation of CD8 T cells that causes skin inflammation, and that suppressive activity of MHC class II - LAG3 interaction ameliorates dermatitis development.
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页码:1173 / 1189
页数:17
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