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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.

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。

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