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Notch 调控早期胸腺细胞发育。

Notch regulation of early thymocyte development.

机构信息

The Department of Pathology & Laboratory Medicine and the Abramson Family Cancer Research Institute at the University of Pennsylvania School of Medicine, Philadelphia, PA, USA.

出版信息

Semin Immunol. 2010 Oct;22(5):261-9. doi: 10.1016/j.smim.2010.04.015. Epub 2010 Jul 13.

DOI:10.1016/j.smim.2010.04.015
PMID:20630772
Abstract

Notch signaling plays multiple roles in T cell development. Following thymic entry, Notch signals are required to specify the T cell fate from a multipotent hematopoietic progenitor. At subsequent steps in early T cell development, Notch provides important differentiation, survival, proliferation and metabolic signals. This review focuses on the multiple functions of Notch in early T cell development, from T cell specification in the thymus through beta selection.

摘要

Notch 信号通路在 T 细胞发育中发挥多种作用。在进入胸腺后,Notch 信号对于从多能造血祖细胞中特异性指定 T 细胞命运是必需的。在早期 T 细胞发育的后续步骤中,Notch 提供了重要的分化、存活、增殖和代谢信号。本综述重点介绍了 Notch 在早期 T 细胞发育中的多种功能,从胸腺中的 T 细胞特异性到β选择。

相似文献

1
Notch regulation of early thymocyte development.Notch 调控早期胸腺细胞发育。
Semin Immunol. 2010 Oct;22(5):261-9. doi: 10.1016/j.smim.2010.04.015. Epub 2010 Jul 13.
2
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Microenvironmental regulation of T cell development in the thymus.胸腺中T细胞发育的微环境调节
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Delta-like 4 is indispensable in thymic environment specific for T cell development.Delta样蛋白4在胸腺环境中对T细胞发育具有不可或缺的作用。
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Differential requirements for Wnt and Notch signaling in hematopoietic versus thymic niches.造血微环境与胸腺微环境中 Wnt 和 Notch 信号的差异需求。
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Delta-like 4-mediated Notch signaling is required for early T-cell development in a three-dimensional thymic structure.Delta样4介导的Notch信号对于三维胸腺结构中早期T细胞发育是必需的。
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Fate of hematopoietic stem cells determined by Notch1 signaling (Review).
Notch1信号通路决定造血干细胞的命运(综述)
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MicroRNAs as Modulators of the Immune Response in T-Cell Acute Lymphoblastic Leukemia.微小 RNA 作为 T 细胞急性淋巴细胞白血病免疫反应的调节剂。
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PHF6 Expression Levels Impact Human Hematopoietic Stem Cell Differentiation.PHF6表达水平影响人类造血干细胞分化。
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How transcription factors drive choice of the T cell fate.转录因子如何驱动 T 细胞命运的选择。
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Quantitative analysis reveals reciprocal regulations underlying recovery dynamics of thymocytes and thymic environment in mice.定量分析揭示了小鼠胸腺细胞和胸腺微环境恢复动态的相互调节作用。
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