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本文引用的文献

1
Mammalian target of rapamycin protein complex 2 regulates differentiation of Th1 and Th2 cell subsets via distinct signaling pathways.雷帕霉素蛋白复合物2的哺乳动物靶点通过不同的信号通路调节Th1和Th2细胞亚群的分化。
Immunity. 2010 Jun 25;32(6):743-53. doi: 10.1016/j.immuni.2010.06.002.
2
E-selectin engages PSGL-1 and CD44 through a common signaling pathway to induce integrin alphaLbeta2-mediated slow leukocyte rolling.E-选择素通过一条共同的信号通路与 PSGL-1 和 CD44 结合,诱导整合素 αLβ2 介导的白细胞缓慢滚动。
Blood. 2010 Jul 22;116(3):485-94. doi: 10.1182/blood-2009-12-259556. Epub 2010 Mar 18.
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CD44 regulates survival and memory development in Th1 cells.CD44 调节 Th1 细胞的存活和记忆发育。
Immunity. 2010 Jan 29;32(1):104-15. doi: 10.1016/j.immuni.2009.10.011. Epub 2010 Jan 14.
4
CD44 costimulation promotes FoxP3+ regulatory T cell persistence and function via production of IL-2, IL-10, and TGF-beta.CD44共刺激通过产生白细胞介素-2、白细胞介素-10和转化生长因子-β促进FoxP3 +调节性T细胞的持久性和功能。
J Immunol. 2009 Aug 15;183(4):2232-41. doi: 10.4049/jimmunol.0900191. Epub 2009 Jul 27.
5
mTOR: taking cues from the immune microenvironment.mTOR:从免疫微环境中获取线索。
Immunology. 2009 Aug;127(4):459-65. doi: 10.1111/j.1365-2567.2009.03125.x.
6
CD44 and its role in inflammation and inflammatory diseases.CD44 及其在炎症和炎性疾病中的作用。
Inflamm Allergy Drug Targets. 2009 Jul;8(3):208-20. doi: 10.2174/187152809788680994.
7
Rheostatic signaling by CD44 and hyaluronan.CD44与透明质酸的变阻信号传导
Cell Signal. 2009 May;21(5):651-5. doi: 10.1016/j.cellsig.2009.01.024. Epub 2009 Jan 13.
8
Mechanisms of chemokine and antigen-dependent T-lymphocyte navigation.趋化因子和抗原依赖性T淋巴细胞导航机制。
Biochem J. 2009 Feb 15;418(1):13-27. doi: 10.1042/BJ20081969.
9
CD44 mediates successful interstitial navigation by killer T cells and enables efficient antitumor immunity.CD44介导杀伤性T细胞成功进行间质导航,并实现高效抗肿瘤免疫。
Immunity. 2008 Dec 19;29(6):971-85. doi: 10.1016/j.immuni.2008.10.015.
10
Hyaluronan induces cell death in activated T cells through CD44.透明质酸通过CD44诱导活化T细胞死亡。
J Immunol. 2008 Nov 15;181(10):7044-54. doi: 10.4049/jimmunol.181.10.7044.

CD44对T细胞的多方面调控

Multifaceted regulation of T cells by CD44.

作者信息

Baaten Bas Jg, Li Cheng-Rui, Bradley Linda M

机构信息

Infectious and Inflammatory Diseases Center; Sanford-Burnham Medical Research Institute; La Jolla, CA USA.

出版信息

Commun Integr Biol. 2010 Nov;3(6):508-12. doi: 10.4161/cib.3.6.13495. Epub 2010 Nov 1.

DOI:10.4161/cib.3.6.13495
PMID:21331226
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3038050/
Abstract

CD44 is a widely-expressed adhesion receptor that is associated with diverse biological processes involving migrating cells, including inflammation, angiogenesis, bone metabolism and wound healing. In the immune system, CD44 is upregulated after activation of naive T lymphocytes during their responses against invading microbes. Once an infection is cleared, elevated levels of CD44 remain on the surface of memory T cells that mediate protection against re-infection. While this has led to the use of highly sustained CD44 expression on T cells as an indicator of a previous immune response, the relevance to T-cell responses or homeostasis has been largely unexplored. Our recent studies demonstrate that CD44 selectively regulates the survival of the Th1 subset of CD4 T cells, but not other T-cell subpopulations. These findings, together with studies of CD44 in other cell types, suggest that differences in the engagement of signaling mechanisms are likely to underlie differential regulation of T-cell responses and underscore the importance of this adhesion receptor to immune cell regulation and protection against viruses and intracellular bacteria.

摘要

CD44是一种广泛表达的黏附受体,与涉及迁移细胞的多种生物学过程相关,包括炎症、血管生成、骨代谢和伤口愈合。在免疫系统中,初始T淋巴细胞在对入侵微生物作出反应时被激活后,CD44表达上调。一旦感染清除,CD44的高水平表达仍保留在介导针对再次感染的保护作用的记忆T细胞表面。虽然这已导致将T细胞上高度持续的CD44表达用作先前免疫反应的指标,但CD44与T细胞反应或稳态的相关性在很大程度上尚未得到探索。我们最近的研究表明,CD44选择性地调节CD4 T细胞的Th1亚群的存活,但不调节其他T细胞亚群。这些发现,连同对其他细胞类型中CD44的研究,表明信号传导机制参与的差异可能是T细胞反应差异调节的基础,并强调了这种黏附受体对免疫细胞调节以及抵抗病毒和细胞内细菌的重要性。