Lee J R, Koretzky G A
Department of Internal Medicine, College of Medicine, University of Iowa, Iowa City 52242, USA.
Eur J Immunol. 1998 Dec;28(12):4188-97. doi: 10.1002/(SICI)1521-4141(199812)28:12<4188::AID-IMMU4188>3.0.CO;2-B.
Recent studies indicate that reactive oxygen intermediates (ROI) serve as second messengers in cell signaling. ROI have been implicated in the activation of NF-kappaB as well as c-Jun N-terminal kinase (JNK) in response to IL-1 and TNF-alpha stimulation. In this report we examine whether intracellular ROI are involved in CD40 receptor signaling. We show that CD40 engagement on resting splenic B lymphocytes and murine B lymphoma WEHI 231 cells generates ROI. Blocking ROI production by preincubation with the antioxidant N-acetyl-L-cysteine inhibits JNK activation, NF-kappaB-driven luciferase activity, and IL-6 secretion following CD40 ligation, suggesting a role for ROI in CD40-mediated signaling events. Furthermore, transfection of WEHI 231 cells with a plasmid encoding Mn-superoxide dismutase interferes with CD40-induced NF-kappaB activation, providing further support for ROI involvement in this pathway. Collectively, these data demonstrate that ROI may serve as second messengers linking CD40 engagement on B cells to important downstream activation events.
最近的研究表明,活性氧中间体(ROI)在细胞信号传导中充当第二信使。ROI与在对IL-1和TNF-α刺激的应答中NF-κB以及c-Jun N端激酶(JNK)的激活有关。在本报告中,我们研究细胞内ROI是否参与CD40受体信号传导。我们发现,在静息脾B淋巴细胞和鼠B淋巴瘤WEHI 231细胞上CD40的结合会产生ROI。用抗氧化剂N-乙酰-L-半胱氨酸预孵育来阻断ROI的产生,会抑制CD40连接后的JNK激活、NF-κB驱动的荧光素酶活性以及IL-6分泌,提示ROI在CD40介导的信号事件中发挥作用。此外,用编码锰超氧化物歧化酶的质粒转染WEHI 231细胞会干扰CD40诱导的NF-κB激活,为ROI参与此途径提供了进一步支持。总体而言,这些数据表明ROI可能作为第二信使,将B细胞上CD40的结合与重要的下游激活事件联系起来。