Queen Mary University of London, William Harvey Research Institute, UK.
Autoimmun Rev. 2012 Sep;11(11):795-8. doi: 10.1016/j.autrev.2012.02.007. Epub 2012 Feb 12.
CD5(+) B lymphocytes have distinct functional properties compared with B lymphocytes that lack CD5. However, it remains unclear if and how the CD5 molecule modulates B lymphocyte biology and responses. Our recent studies have revealed that CD5 promotes constitutive activation of multiple signaling pathways including extracellular signal-regulated kinases (ERK1/2), phosphatidylinositol 3-kinase (PI-3K)/mammalian target of rapamycin (mTOR) and calcineurin-NFAT signaling pathways. Further, changes in cytokine production including the production of IL-10 are related to the activation of the transcription factors NFAT2 and STAT3. All in all, these studies provide a framework for understanding how CD5 impacts B lymphocyte biology and responses.
CD5(+) B 淋巴细胞与缺乏 CD5 的 B 淋巴细胞具有明显不同的功能特性。然而,目前尚不清楚 CD5 分子是否以及如何调节 B 淋巴细胞的生物学和反应。我们最近的研究表明,CD5 促进包括细胞外信号调节激酶 (ERK1/2)、磷脂酰肌醇 3-激酶 (PI-3K)/雷帕霉素靶蛋白 (mTOR) 和钙调神经磷酸酶-NFAT 信号通路在内的多种信号通路的组成性激活。此外,细胞因子产生的变化,包括 IL-10 的产生,与转录因子 NFAT2 和 STAT3 的激活有关。总而言之,这些研究为理解 CD5 如何影响 B 淋巴细胞的生物学和反应提供了一个框架。