TY - JOUR
T1 - The Four-and-a-Half LIM Domain Protein 2 Supports Influenza A Virus–Induced Lung Inflammation by Restricting the Host Adaptive Immune Response
AU - Masemann, Dörthe
AU - Leite Dantas, Rafael
AU - Sitnik, Siarhei
AU - Schied, Tanja
AU - Nordhoff, Carolin
AU - Ludwig, Stephan
AU - Wixler, Viktor
N1 - Publisher Copyright:
© 2018 American Society for Investigative Pathology
PY - 2018/5/1
Y1 - 2018/5/1
N2 - Four-and-a-half LIM domain protein 2 (FHL2) is a multifunctional adaptor protein with fine-tuning adjustment properties. It acts as a regulator of signaling cascades but also as a cofactor of transcription and controls several anti-inflammatory immune responses. Recently, we described FHL2 as a novel regulator of influenza A virus propagation. We have shown that in vitro FHL2 restricts viral replication by accelerating the interferon regulatory factor 3–dependent transcription of the Ifnb1 gene. In this work, we unraveled an ambiguous role of FHL2 during influenza A virus infection in vivo. Although FHL2 restrained viral replication during the first 24 hours of infection, it significantly delayed viral clearance afterward. Comparison of lung immune status of wild-type and FHL2 knockout mice during influenza virus infection did not acknowledge significant differences in the innate host immune response but revealed an improved migration of dendritic cells from infected lungs into draining lymph nodes as well as increased levels of activated CD8 + T lymphocytes accumulated in the lungs of FHL2 knockout mice.
AB - Four-and-a-half LIM domain protein 2 (FHL2) is a multifunctional adaptor protein with fine-tuning adjustment properties. It acts as a regulator of signaling cascades but also as a cofactor of transcription and controls several anti-inflammatory immune responses. Recently, we described FHL2 as a novel regulator of influenza A virus propagation. We have shown that in vitro FHL2 restricts viral replication by accelerating the interferon regulatory factor 3–dependent transcription of the Ifnb1 gene. In this work, we unraveled an ambiguous role of FHL2 during influenza A virus infection in vivo. Although FHL2 restrained viral replication during the first 24 hours of infection, it significantly delayed viral clearance afterward. Comparison of lung immune status of wild-type and FHL2 knockout mice during influenza virus infection did not acknowledge significant differences in the innate host immune response but revealed an improved migration of dendritic cells from infected lungs into draining lymph nodes as well as increased levels of activated CD8 + T lymphocytes accumulated in the lungs of FHL2 knockout mice.
UR - http://www.scopus.com/inward/record.url?scp=85045072207&partnerID=8YFLogxK
U2 - 10.1016/j.ajpath.2018.02.004
DO - 10.1016/j.ajpath.2018.02.004
M3 - Article
C2 - 29458009
AN - SCOPUS:85045072207
SN - 0002-9440
VL - 188
SP - 1236
EP - 1245
JO - American Journal of Pathology
JF - American Journal of Pathology
IS - 5
ER -