Department of Microbiology, Immunology and Infectious Diseases, University of Calgary, Calgary, AB, Canada.
Changzhou Key Laboratory of Molecular Diagnostics and Precision Cancer Medicine, Changzhou Wujin People's Hospital, Changzhou Medical Center, Nanjing Medical University, Changzhou, China.
Methods Mol Biol. 2025;2854:117-125. doi: 10.1007/978-1-0716-4108-8_13.
Beyond its role as the bearer of genetic material, DNA also plays a crucial role in the activation phase of innate immunity. Pathogen recognition receptors (PRRs) and their homologs, pathogen-associated molecular patterns (PAMPs), form the foundation for driving innate immune activation and the induction of immune responses during infection. In the context of DNA viruses or bacterial infections, specific DNA sequences are recognized and bound by DNA sensors, marking the DNA as a PAMP for host recognition and subsequent activation of innate immunity. The primary DNA sensor pathway known to date is cGAS-STING, which can induce Type I interferons (IFN) and innate immune responses against viruses and bacteria. Additionally, the cGAS-STING pathway has been identified to mediate functions in autophagy and senescence. Herein, we introduce methods for using DNA PAMPs as molecular tools to study the role of cGAS-STING and its signaling pathway in regulating innate immunity, both in vitro and in vivo.
除了作为遗传物质的载体外,DNA 在先天免疫的激活阶段也起着至关重要的作用。病原体识别受体(PRRs)及其同源物、病原体相关分子模式(PAMPs)为驱动先天免疫激活和诱导感染期间免疫反应奠定了基础。在 DNA 病毒或细菌感染的情况下,特定的 DNA 序列被 DNA 传感器识别和结合,将 DNA 标记为宿主识别的 PAMP,并随后激活先天免疫。迄今为止已知的主要 DNA 传感器途径是 cGAS-STING,它可以诱导 I 型干扰素(IFN)和针对病毒和细菌的先天免疫反应。此外,cGAS-STING 途径已被确定介导自噬和衰老的功能。本文介绍了使用 DNA PAMPs 作为分子工具的方法,用于研究 cGAS-STING 及其信号通路在调节先天免疫中的作用,包括体外和体内。