Two waves of pro-inflammatory factors are released during the influenza A virus (IAV)-driven pulmonary immunopathogenesis
Two waves of pro-inflammatory factors are released during the influenza A virus (IAV)-driven pulmonary immunopathogenesis
复制标题
甲型流感病毒 (IAV) 驱动的肺部免疫发病过程中释放两波促炎因子
DOI:
10.1371/journal.ppat.1008334
复制
发表时间:
2020-02
期刊:
影响因子:
6.7
通讯作者:
Zhang Hui
中科院分区:
文献类型:
--
作者:
Zhang Junsong;Liu Jun;Yuan Yaochang;Huang Feng;Ma Rong;Luo Baohong;Xi Zhihui;Pan Ting;Liu Bingfeng;Zhang Yiwen;Zhang Xu;Luo Yuewen;Wang Jin;Zhao Meng;Lu Gen;Deng Kai;Zhang Hui
Influenza A virus (IAV) infection is a complicated process. After IAVs spread to the lung, extensive pro-inflammatory cytokines and chemokines are released, which largely determine the outcome of infection. Using a single-cell RNA sequencing (scRNA-seq) assay, we systematically and sequentially analyzed the transcriptome of more than 16,000 immune cells in the pulmonary tissue of infected mice, and demonstrated that two waves of pro-inflammatory factors were released. A group of IAV-infected PD-L1+ neutrophils were the major contributor to the first wave at an earlier stage (day 1–3 post infection). Notably, at a later stage (day 7 post infection) when IAV was hardly detected in the immune cells, a group of platelet factor 4-positive (Pf4+)-macrophages generated another wave of pro-inflammatory factors, which were probably the precursors of alveolar macrophages (AMs). Furthermore, single-cell signaling map identified inter-lineage crosstalk between different clusters and helped better understand the signature of PD-L1+ neutrophils and Pf4+-macrophages. Our data characteristically clarified the infiltrated immune cells and their production of pro-inflammatory factors during the immunopathogenesis development, and deciphered the important mechanisms underlying IAV-driven inflammatory reactions in the lung.
登录
查看更多内容
DOI:
10.4337/9781783474684.00062
发表时间:
2019
期刊:
Concepts for International Law
影响因子:
--
作者:
Mario Prost
通讯作者:
Mario Prost
DOI:
10.1126/science.1247651
发表时间:
2014-02-14
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Jaitin DA;Kenigsberg E;Keren-Shaul H;Elefant N;Paul F;Zaretsky I;Mildner A;Cohen N;Jung S;Tanay A;Amit I
通讯作者:
Amit I
DOI:
10.1084/jem.20162152
发表时间:
2017-08-07
期刊:
The Journal of experimental medicine
影响因子:
--
作者:
Misharin AV;Morales-Nebreda L;Reyfman PA;Cuda CM;Walter JM;McQuattie-Pimentel AC;Chen CI;Anekalla KR;Joshi N;Williams KJN;Abdala-Valencia H;Yacoub TJ;Chi M;Chiu S;Gonzalez-Gonzalez FJ;Gates K;Lam AP;Nicholson TT;Homan PJ;Soberanes S;Dominguez S;Morgan VK;Saber R;Shaffer A;Hinchcliff M;Marshall SA;Bharat A;Berdnikovs S;Bhorade SM;Bartom ET;Morimoto RI;Balch WE;Sznajder JI;Chandel NS;Mutlu GM;Jain M;Gottardi CJ;Singer BD;Ridge KM;Bagheri N;Shilatifard A;Budinger GRS;Perlman H
通讯作者:
Perlman H
DOI:
10.1073/pnas.1902840116
发表时间:
2019-05-28
影响因子:
11.1
作者:
Kudo, Eriko;Song, Eric;Iwasaki, Akiko
通讯作者:
Iwasaki, Akiko
影响因子:
16.6
作者:
Zheng GX;Terry JM;Belgrader P;Ryvkin P;Bent ZW;Wilson R;Ziraldo SB;Wheeler TD;McDermott GP;Zhu J;Gregory MT;Shuga J;Montesclaros L;Underwood JG;Masquelier DA;Nishimura SY;Schnall-Levin M;Wyatt PW;Hindson CM;Bharadwaj R;Wong A;Ness KD;Beppu LW;Deeg HJ;McFarland C;Loeb KR;Valente WJ;Ericson NG;Stevens EA;Radich JP;Mikkelsen TS;Hindson BJ;Bielas JH
通讯作者:
Bielas JH