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本文引用的文献

1
Notch signaling and T-helper cells in EAE/MS.实验性自身免疫性脑脊髓炎/多发性硬化症中的Notch信号通路与辅助性T细胞
Clin Dev Immunol. 2013;2013:570731. doi: 10.1155/2013/570731. Epub 2013 Nov 14.
2
IRF4 controls the positioning of mature B cells in the lymphoid microenvironments by regulating NOTCH2 expression and activity.IRF4 通过调节 NOTCH2 的表达和活性来控制成熟 B 细胞在淋巴微环境中的定位。
J Exp Med. 2013 Dec 16;210(13):2887-902. doi: 10.1084/jem.20131026. Epub 2013 Dec 9.
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Regulation of innate and adaptive immunity by Notch.Notch 对固有免疫和适应性免疫的调节。
Nat Rev Immunol. 2013 Jun;13(6):427-37. doi: 10.1038/nri3445. Epub 2013 May 13.
4
The kinase PDK1 is essential for B-cell receptor mediated survival signaling.蛋白激酶 PDK1 是 B 细胞受体介导的存活信号转导所必需的。
PLoS One. 2013;8(2):e55378. doi: 10.1371/journal.pone.0055378. Epub 2013 Feb 5.
5
Characterization of CSL (CBF-1, Su(H), Lag-1) mutants reveals differences in signaling mediated by Notch1 and Notch2.CSL(CBF-1、Su(H)、Lag-1)突变体的特征分析揭示了 Notch1 和 Notch2 介导的信号转导的差异。
J Biol Chem. 2012 Oct 12;287(42):34904-34916. doi: 10.1074/jbc.M112.403287. Epub 2012 Aug 22.
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The Notch signalling system: recent insights into the complexity of a conserved pathway.Notch 信号通路系统:对保守通路复杂性的最新见解。
Nat Rev Genet. 2012 Sep;13(9):654-66. doi: 10.1038/nrg3272. Epub 2012 Aug 7.
7
Notch receptor-ligand interactions during T cell development, a ligand endocytosis-driven mechanism.Notch 受体-配体相互作用在 T 细胞发育过程中,是一种配体内吞驱动的机制。
Curr Top Microbiol Immunol. 2012;360:19-46. doi: 10.1007/82_2012_225.
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Notch ligands expressed by follicular dendritic cells protect germinal center B cells from apoptosis.滤泡树突状细胞表达的Notch配体可保护生发中心B细胞免于凋亡。
J Immunol. 2009 Jul 1;183(1):352-8. doi: 10.4049/jimmunol.0803183.
9
Constitutively activated Notch signaling is involved in survival and apoptosis resistance of B-CLL cells.组成性激活的Notch信号通路参与B细胞慢性淋巴细胞白血病(B-CLL)细胞的存活和抗凋亡过程。
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10
Aberrant expression of Notch1 interferes with the B-lymphoid phenotype of neoplastic B cells in classical Hodgkin lymphoma.Notch1的异常表达会干扰经典型霍奇金淋巴瘤中肿瘤性B细胞的B淋巴细胞表型。
Leukemia. 2008 Aug;22(8):1587-94. doi: 10.1038/leu.2008.101. Epub 2008 May 1.

Notch1是Notch配体增强B细胞活化和抗体分泌的重要介质。

Notch1 is an important mediator for enhancing of B-cell activation and antibody secretion by Notch ligand.

作者信息

Kang Jung-Ah, Kim Woo-Seok, Park Sung-Gyoo

机构信息

School of Life Sciences, Gwangju Institute of Science and Technology (GIST), Gwangju, Korea; Bio Imaging Research Centre and Immune Synapse Research Centre, Gwangju Institute of Science and Technology (GIST), Gwangju, Korea.

出版信息

Immunology. 2014 Dec;143(4):550-9. doi: 10.1111/imm.12333.

DOI:10.1111/imm.12333
PMID:24913005
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4253503/
Abstract

The roles of Notch1 and Notch2 in T-cell function have been well studied, but the functional roles of Notch in B cells have not been extensively investigated, except for Notch2 involvement in peripheral marginal zone B-cell differentiation. This study examined the roles of Notch1 in murine primary B cells. During B-cell activation by B-cell receptor ligation, Notch1 was up-regulated while Notch2 was not. In addition, Notch1 up-regulation itself did not contribute to the further activation of B cells, but the Notch ligand was important for Notch1-mediated further B-cell activation. Moreover, Notch1 deficiency significantly decreased B-cell activation and antibody secretion under the presence of Notch ligand. These data suggest that Notch1 is an important mediator for enhancing B-cell activation and antibody secretion by Notch ligand.

摘要

Notch1和Notch2在T细胞功能中的作用已得到充分研究,但除了Notch2参与外周边缘区B细胞分化外,Notch在B细胞中的功能作用尚未得到广泛研究。本研究检测了Notch1在小鼠原代B细胞中的作用。在通过B细胞受体连接激活B细胞的过程中,Notch1上调而Notch2未上调。此外,Notch1上调本身并不有助于B细胞的进一步激活,但Notch配体对于Notch1介导的B细胞进一步激活很重要。此外,在存在Notch配体的情况下,Notch1缺陷显著降低了B细胞激活和抗体分泌。这些数据表明,Notch1是Notch配体增强B细胞激活和抗体分泌的重要介质。