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Stat5a通过多种不同机制调节辅助性T细胞分化。

Stat5a regulates T helper cell differentiation by several distinct mechanisms.

作者信息

Kagami S, Nakajima H, Suto A, Hirose K, Suzuki K, Morita S, Kato I, Saito Y, Kitamura T, Iwamoto I

机构信息

Department of Internal Medicine II, Chiba University School of Medicine, Japan.

出版信息

Blood. 2001 Apr 15;97(8):2358-65. doi: 10.1182/blood.v97.8.2358.

Abstract

We have previously shown that CD4(+) T cell-mediated allergic inflammation is diminished in signal transducer and activator of transcription (Stat)5a-deficient (Stat5a(-/-)) mice. To determine whether Stat5a regulates T helper cell differentiation, we studied T helper (Th)1 and Th2 cell differentiation of Stat5a(-/-)CD4(+) T cells at single-cell levels. First, Th2 cell differentiation from antigen-stimulated splenocytes was significantly decreased in Stat5a(-/-) mice as compared with that in wild-type mice. Further, Th2 cell differentiation was also impaired in Stat5a(-/-) mice even when purified CD4(+) T cells were stimulated with anti-CD3 plus anti-CD28 antibodies in the presence of interleukin-4. Moreover, the retrovirus-mediated gene expression of Stat5a in Stat5a(-/-)CD4(+) T cells restored the Th2 cell differentiation at the similar levels to that in wild-type CD4(+) T cells. In addition, interleukin-4 normally phosphorylated Stat6 in CD4(+) T cells from Stat5a(-/-) mice. Second, the development of CD4(+)CD25(+) immunoregulatory T cells was impaired in Stat5a(-/-) mice, as indicated by a significant decrease in the number of CD4(+)CD25(+) T cells in Stat5a(-/-) mice. Furthermore, the depletion of CD4(+)CD25(+) T cells from wild-type splenocytes significantly decreased Th2 cell differentiation but increased Th1 cell differentiation, whereas the depletion of CD4(+)CD25(+) T cells from Stat5a(-/-) splenocytes had no significant effect on the Th1 and Th2 cell differentiation. Together, these results indicate that the intrinsic expression of Stat5a in CD4(+) T cells is required for Th2 cell differentiation and that Stat5a is involved in the development of CD4(+)CD25(+) immunoregulatory T cells that modulate T helper cell differentiation toward Th2 cells.

摘要

我们之前已经表明,在信号转导子和转录激活子(Stat)5a缺陷(Stat5a(-/-))小鼠中,CD4(+) T细胞介导的过敏性炎症有所减轻。为了确定Stat5a是否调节辅助性T细胞分化,我们在单细胞水平研究了Stat5a(-/-) CD4(+) T细胞的辅助性T(Th)1和Th2细胞分化。首先,与野生型小鼠相比,Stat5a(-/-)小鼠中抗原刺激的脾细胞向Th2细胞的分化显著减少。此外,即使在用白细胞介素-4存在的情况下用抗CD3加抗CD28抗体刺激纯化的CD4(+) T细胞时,Stat5a(-/-)小鼠中的Th2细胞分化也受到损害。此外,Stat5a(-/-) CD4(+) T细胞中逆转录病毒介导的Stat5a基因表达将Th2细胞分化恢复到与野生型CD4(+) T细胞相似的水平。另外,白细胞介素-4正常磷酸化Stat5a(-/-)小鼠CD4(+) T细胞中的Stat6。其次,Stat5a(-/-)小鼠中CD4(+)CD25(+)免疫调节性T细胞的发育受损,这表现为Stat5a(-/-)小鼠中CD4(+)CD25(+) T细胞数量显著减少。此外,从野生型脾细胞中耗尽CD4(+)CD25(+) T细胞显著降低Th2细胞分化但增加Th1细胞分化,而从Stat5a(-/-)脾细胞中耗尽CD4(+)CD25(+) T细胞对Th1和Th2细胞分化没有显著影响。总之,这些结果表明CD4(+) T细胞中Stat5a的内在表达是Th2细胞分化所必需的,并且Stat5a参与调节辅助性T细胞向Th2细胞分化的CD4(+)CD25(+)免疫调节性T细胞的发育。

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