Overexpression of AML1 transcription factor drives thymocytes into the CD8 single-positive lineage

被引:54
作者
Hayashi, K
Abe, N
Watanabe, T
Obinata, M
Ito, M
Sato, T
Habu, S
Satake, M
机构
[1] Tohoku Univ, Dept Mol Immunol, Inst Dev Aging & Canc, Aoba Ku, Sendai, Miyagi 9808575, Japan
[2] Tohoku Univ, Dept Cell Biol, Inst Dev Aging & Canc, Aoba Ku, Sendai, Miyagi 9808575, Japan
[3] Cent Inst Expt Anim, Kawasaki, Kanagawa, Japan
[4] Tokai Univ, Sch Med, Dept Immunol, Isehara, Kanagawa 25911, Japan
关键词
D O I
10.4049/jimmunol.167.9.4957
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To understand the gene regulation involved in the development of single-positive (SP) thymocytes, we generated transgenic mice in which the AML1 transcription factor is overexpressed. In these mice the number of CD8 SP thymocytes was greatly increased, and this continued to be true even when MHC class I was absent. This promotion to the CDS SP lineage was not, however, observed when both class I and class II were absent. Furthermore, even thymocytes carrying MHC class II-restricted TCR differentiated into the CD8 SP lineage when AML1 was overexpressed. The selected CD8 SP cells were, however, unable to mature, as judged by the expression level of heat-stable Ag. Thus, overexpression of AML1 is able to skew class II-restricted thymocytes into the CD8 SP lineage, but not to drive the maturation of resulting selected CDS SP cells.
引用
收藏
页码:4957 / 4965
页数:9
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