疟蚊 NF-κB 调控的剪接因子指导高度可变的模式识别受体 AgDscam 产生病原体特异性的反应谱。

Anopheles NF-κB-regulated splicing factors direct pathogen-specific repertoires of the hypervariable pattern recognition receptor AgDscam.

机构信息

W. Harry Feinstone Department of Molecular Microbiology and Immunology, Bloomberg School of Public Health, Johns Hopkins University, 615 North Wolfe Street, Baltimore, MD 21205-2179, USA.

出版信息

Cell Host Microbe. 2012 Oct 18;12(4):521-30. doi: 10.1016/j.chom.2012.09.004.

Abstract

Insects rely on innate immune responses controlled by the immune deficiency (IMD), Toll, and other immune signaling pathways to combat infection by a broad spectrum of pathogens. These pathways signal to downstream NF-κB family transcription factors that control specific antipathogen action via direct transcriptional control of immune effectors, hematopoiesis, and melanization. Here we show that in the Anopheles malaria vector, IMD and Toll pathways mediate species-specific defenses against Plasmodium and bacteria through the transcriptional regulation of splicing factors Caper and IRSF1 that, in turn, determine the production of pathogen-specific splice variant repertoires of the hypervariable pattern recognition receptor AgDscam. This mechanism represents an additional level of immune response regulation that may provide a previously unrecognized level of plasticity to the insect immune pathway-regulated antipathogen defenses.

摘要

昆虫依赖于先天免疫反应,这些反应由免疫缺陷(IMD)、Toll 和其他免疫信号通路控制,以抵御广谱病原体的感染。这些通路向下游 NF-κB 家族转录因子发出信号,通过直接转录控制免疫效应物、造血和黑化来控制特定的抗病原体作用。在这里,我们表明在疟疾病媒按蚊中,IMD 和 Toll 通路通过剪接因子 Caper 和 IRSF1 的转录调控来介导针对疟原虫和细菌的种特异性防御,而剪接因子 Caper 和 IRSF1 又决定了高度可变的模式识别受体 AgDscam 的病原体特异性剪接变体谱的产生。这种机制代表了免疫反应调节的另一个层次,可能为昆虫免疫途径调节的抗病原体防御提供了以前未被认识到的可塑性水平。

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