选择素促进SARS-CoV-2与血小板和内皮的相互作用
Cesar L Moreno1,2, Fernanda Vs Castanheira3, Alberto Ospina Stella2
1Dr. John and Anne Chong Lab for Functional Genomics, Charles Perkins Centre and School of Life and Environmental Sciences, The University of Sydney, Sydney, New South Wales, Australia.
研究人员确定了与SARS-CoV-2感染作斗争的宿主基因. 发现P selectin是一种先天性免疫受体,可以阻止病毒的进入和感染,为冠状病毒疾病提供潜在的治疗标.
科学领域:
- 病毒学 病毒学
- 免疫学 免疫学 免疫学
- 遗传学 遗传学 是一个
背景情况:
- 宿主-病原体相互作用对于理解病毒感染至关重要.
- 影响SARS-CoV-2感染的特定宿主因素在很大程度上仍未被描述.
研究的目的:
- 使用CRISPR激活屏幕识别提供对SARS-CoV-2感染耐药性的宿主基因.
- 阐明已识别的基因,特别是P选择素在SARS-CoV-2病变发生过程中的作用.
主要方法:
- 克里斯普尔激活查以确定影响SARS-CoV-2耐药性的宿主基因.
- 使用真实SARS-CoV-2的候选基因验证.
- 评估P选择素在病毒结合,感染和血小板/内皮相互作用中的作用.
主要成果:
- 发现了34个新的候选宿主基因.
- 包括P selectin在内的7个基因被证实可以抑制SARS-CoV-2感染.
- 选择因增强SARS-CoV-2尖端与细胞和血小板的结合,促进体内病毒的归宿,并阻止这些相互作用清除感染.
结论:
- 素在SARS-CoV-2感染中发挥着重要作用,通过调解与血小板和内皮的病毒相互作用.
- 素的功能扩展到其他致病性冠状病毒.
- 涉及Pselectin调节的治疗策略,如mRNA驱动的表达,显示出阻断SARS-CoV-2感染的希望.
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