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组成型前T细胞受体信号通过钙离子动员以及核因子κB和活化T细胞核因子的激活来促进分化。

Constitutive pre-TCR signaling promotes differentiation through Ca2+ mobilization and activation of NF-kappaB and NFAT.

作者信息

Aifantis I, Gounari F, Scorrano L, Borowski C, von Boehmer H

机构信息

Department of Pathology, Harvard Medical School, Dana-Farber Cancer Institute, Boston, MA 02115, USA.

出版信息

Nat Immunol. 2001 May;2(5):403-9. doi: 10.1038/87704.

Abstract

Pre-T cell antigen receptor (pre-TCR) signaling plays a crucial role in the development of immature T cells. Although certain aspects of proximal pre-TCR signaling have been studied, the intermediate signal transducers and the distal transcription modulators have been poorly characterized. We report here a correlation between pre-TCR signaling and a biphasic rise in the cytosolic Ca2+ concentration. In addition, we show that constitutive pre-TCR signaling is associated with an increased rate of Ca2+ influx through store-operated plasma membrane Ca2+ channels. We show also that the biphasic nature of the observed pre-TCR-induced rise in cytosolic Ca2+ differentially modulates the activities of the transcription factors NF-kappaB and NFAT in developing T cells.

摘要

前T细胞抗原受体(pre-TCR)信号传导在未成熟T细胞的发育中起着关键作用。尽管近端pre-TCR信号传导的某些方面已得到研究,但中间信号转导分子和远端转录调节因子的特征却鲜为人知。我们在此报告pre-TCR信号传导与胞质Ca2+浓度的双相升高之间的相关性。此外,我们表明组成型pre-TCR信号传导与通过储存操纵性质膜Ca2+通道的Ca2+内流速率增加有关。我们还表明,观察到的pre-TCR诱导的胞质Ca2+升高的双相性质在发育中的T细胞中差异调节转录因子NF-κB和NFAT的活性。

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