生物
内部收益率3
甲型流感病毒
病毒
病毒复制
免疫学
干扰素
电池类型
病毒学
先天免疫系统
免疫系统
细胞
遗传学
作者
Z. Joel,Wy Ching Ng,Luke Zappia,Linden J. Gearing,Moshe Olshansky,Kym Pham,Karey Cheong,Arthur Hsu,Stephen T. Turner,Odilia L. C. Wijburg,Sarah L. Londrigan,Andrëw G. Brööks,Patrick C. Reading
摘要
Airway epithelial cells (AEC) and airway macrophages (AM) represent major targets of influenza A virus (IAV) infection in the lung, yet the two cell types respond very differently to IAV infection. We have used RNA sequencing to define the host transcriptional responses in each cell type under steady-state conditions as well as following IAV infection. To do this, different cell subsets isolated from the lungs of mock- and IAV-infected mice were subjected to RNA sequencing. Under steady-state conditions, AM and AEC express distinct transcriptional activities, consistent with distinct physiological roles in the airways. Not surprisingly, these cells also exhibited major differences in transcriptional responses following IAV infection. These studies shed light on how the different transcriptional architectures of airway cells from two different lineages drive transcriptional responses to IAV infection.
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