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本文引用的文献

1
The essential role of LAT in thymocyte development during transition from the double-positive to single-positive stage.LAT在胸腺细胞从双阳性向单阳性阶段转变过程中的关键作用。
J Immunol. 2009 May 1;182(9):5596-604. doi: 10.4049/jimmunol.0803170.
2
STAT6 deletion converts the Th2 inflammatory pathology afflicting Lat(Y136F) mice into a lymphoproliferative disorder involving Th1 and CD8 effector T cells.STAT6基因缺失将困扰Lat(Y136F)小鼠的Th2炎症病理转变为一种涉及Th1和CD8效应T细胞的淋巴细胞增殖性疾病。
J Immunol. 2009 Mar 1;182(5):2680-9. doi: 10.4049/jimmunol.0803257.
3
Negative regulation of TCR signaling by linker for activation of X cells via phosphotyrosine-dependent and -independent mechanisms.通过磷酸酪氨酸依赖性和非依赖性机制,X细胞激活连接蛋白对TCR信号传导的负调控。
J Immunol. 2008 Nov 15;181(10):7055-61. doi: 10.4049/jimmunol.181.10.7055.
4
SIT and TRIM determine T cell fate in the thymus.SIT和TRIM决定胸腺中的T细胞命运。
J Immunol. 2008 Nov 1;181(9):5930-9. doi: 10.4049/jimmunol.181.9.5930.
5
Control of lymphocyte development and activation by negative regulatory transmembrane adapter proteins.负性调节跨膜衔接蛋白对淋巴细胞发育和激活的调控
Immunol Rev. 2008 Aug;224:215-28. doi: 10.1111/j.1600-065X.2008.00656.x.
6
Selective impairment of FcepsilonRI-mediated allergic reaction in Gads-deficient mice.Gads基因缺陷小鼠中FcepsilonRI介导的过敏反应的选择性损伤
Int Immunol. 2008 Oct;20(10):1289-97. doi: 10.1093/intimm/dxn085. Epub 2008 Jul 29.
7
Analysis of the linker for activation of T cells and the linker for activation of B cells in natural killer cells reveals a novel signaling cassette, dual usage in ITAM signaling, and influence on development of the Ly49 repertoire.对自然杀伤细胞中T细胞活化连接蛋白和B细胞活化连接蛋白的分析揭示了一种新的信号转导盒、免疫受体酪氨酸活化基序(ITAM)信号传导中的双重作用以及对Ly49受体库发育的影响。
Blood. 2008 Oct 1;112(7):2869-77. doi: 10.1182/blood-2007-11-121590. Epub 2008 Jul 21.
8
Identification of a new transmembrane adaptor protein that constitutively binds Grb2 in B cells.鉴定一种在B细胞中持续结合Grb2的新型跨膜衔接蛋白。
J Leukoc Biol. 2008 Sep;84(3):842-51. doi: 10.1189/jlb.0208087. Epub 2008 Jun 17.
9
Non-T cell activation linker promotes mast cell survival by dampening the recruitment of SHIP1 by linker for activation of T cells.非T细胞激活连接蛋白通过抑制T细胞激活连接蛋白对SHIP1的募集来促进肥大细胞存活。
J Immunol. 2008 Mar 15;180(6):3689-98. doi: 10.4049/jimmunol.180.6.3689.
10
Identification of CKAP4/p63 as a major substrate of the palmitoyl acyltransferase DHHC2, a putative tumor suppressor, using a novel proteomics method.使用一种新型蛋白质组学方法鉴定CKAP4/p63为棕榈酰转移酶DHHC2(一种假定的肿瘤抑制因子)的主要底物。
Mol Cell Proteomics. 2008 Jul;7(7):1378-88. doi: 10.1074/mcp.M800069-MCP200. Epub 2008 Feb 22.

衔接蛋白家族 LAT 在淋巴细胞发育和激活中的调节作用。

Regulation of lymphocyte development and activation by the LAT family of adapter proteins.

机构信息

Department of Immunology, Duke University Medical Center, Durham, NC 27710, USA.

出版信息

Immunol Rev. 2009 Nov;232(1):72-83. doi: 10.1111/j.1600-065X.2009.00828.x.

DOI:10.1111/j.1600-065X.2009.00828.x
PMID:19909357
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3646374/
Abstract

Transmembrane adapter proteins (TRAPs) are critical components of signaling pathways in lymphocytes, linking antigen receptor engagement to downstream cellular processes. While these proteins lack intrinsic enzymatic activity, their phosphorylation following receptor ligation allows them to function as scaffolds for the assembly of multi-molecular signaling complexes. Many TRAPs have recently been discovered, and numerous studies demonstrate their roles in the positive and negative regulation of lymphocyte maturation, activation, and differentiation. One such example is the linker for activation of T cells (LAT) family of adapter proteins. While LAT has been shown to play an indispensable role in T-cell and mast cell function, the other family members, linker for activation of B cells (LAB) and linker for activation of X cells (LAX), are necessary to fine-tune immune responses. In addition to its well-established role in the positive regulation of lymphocyte activation, LAT exerts an inhibitory effect on T-cell receptor-mediated signaling. Furthermore, LAT, along with LAB and LAX, plays a crucial role in establishing and maintaining tolerance. Here, we review recent data concerning the regulation of lymphocyte development and activation by the LAT family of proteins.

摘要

跨膜衔接蛋白(TRAPs)是淋巴细胞信号通路的关键组成部分,将抗原受体的结合与下游细胞过程联系起来。虽然这些蛋白缺乏内在的酶活性,但它们在受体结合后发生的磷酸化使其能够作为多分子信号复合物组装的支架。最近发现了许多 TRAPs,许多研究表明它们在淋巴细胞成熟、激活和分化的正调控和负调控中发挥作用。其中一个例子是 T 细胞激活衔接蛋白(LAT)家族的衔接蛋白。虽然已经证明 LAT 在 T 细胞和肥大细胞功能中发挥不可或缺的作用,但其他家族成员,B 细胞激活衔接蛋白(LAB)和 X 细胞激活衔接蛋白(LAX),对于精细调节免疫反应是必需的。除了其在淋巴细胞激活的正调控中的既定作用外,LAT 对 T 细胞受体介导的信号传递也有抑制作用。此外,LAT 与 LAB 和 LAX 一起,在建立和维持耐受方面发挥着关键作用。在这里,我们回顾了有关 LAT 家族蛋白对淋巴细胞发育和激活的调控的最新数据。