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T细胞分化的分子层面

Molecular aspects of T-cell differentiation.

作者信息

Rao A, Avni O

机构信息

Center for Blood Research, Department of Pathology, Harvard Medical School, Warren Alpert Building, 200 Longwood Avenue, Boston, MA 02115, USA.

出版信息

Br Med Bull. 2000;56(4):969-84. doi: 10.1258/0007142001903634.

Abstract

Differentiated T helper 1 (Th1) and T helper 2 (Th2) T-cells show striking differences in their patterns of cytokine expression. This process is initiated by stimulation with antigen and the cytokines IL-12 and IL-4, respectively, and requires antigen-induced transcription factors such as NFAT and cytokine-induced transcription factors such as STAT4, induced by IL-12, and STAT6, induced by IL-4. This results in induction and maintained expression of subset-specific transcription factors including T-bet in Th1 cells and GATA3 in Th2 cells, which are involved in ensuring the commitment of T-cells to Th1 or Th2 lineages. Here we review the signalling pathways and transcription factors that mediate T-cell differentiation, and describe the epigenetic changes in chromatin structure, locus accessibility and DNA methylation that are known to accompany this process.

摘要

分化的辅助性T细胞1(Th1)和辅助性T细胞2(Th2)在细胞因子表达模式上表现出显著差异。这个过程分别由抗原以及细胞因子白细胞介素12(IL-12)和白细胞介素4(IL-4)刺激启动,并且需要抗原诱导的转录因子如活化T细胞核因子(NFAT)以及细胞因子诱导的转录因子,如IL-12诱导的信号转导和转录激活因子4(STAT4)和IL-4诱导的STAT6。这导致了子集特异性转录因子的诱导和持续表达,包括Th1细胞中的T-bet和Th2细胞中的GATA3,它们参与确保T细胞向Th1或Th2谱系的分化。在这里,我们综述了介导T细胞分化的信号通路和转录因子,并描述了已知伴随这一过程的染色质结构、基因座可及性和DNA甲基化的表观遗传变化。

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