tetano
Editor, Senior Moderator
Life Sci Alliance
. 2023 Apr 18;6(7):e202201837.
doi: 10.26508/lsa.202201837. Print 2023 Jul.
The pro-inflammatory response to influenza A virus infection is fueled by endothelial cells
Lisa Bauer[SUP] 1 [/SUP], Laurine C Rijsbergen[SUP] 2 [/SUP], Lonneke Leijten[SUP] 2 [/SUP], Feline Fw Benavides[SUP] 2 [/SUP], Danny Noack[SUP] 2 [/SUP], Mart M Lamers[SUP] 2 [/SUP], Bart L Haagmans[SUP] 2 [/SUP], Rory D de Vries[SUP] 2 [/SUP], Rik L de Swart[SUP] 2 [/SUP], Debby van Riel[SUP] 3 [/SUP]
Affiliations
Abstract
Morbidity and mortality from influenza are associated with high levels of systemic inflammation. Endothelial cells play a key role in systemic inflammatory responses during severe influenza A virus (IAV) infections, despite being rarely infected in humans. How endothelial cells contribute to systemic inflammatory responses is unclear. Here, we developed a transwell system in which airway organoid-derived differentiated human lung epithelial cells were co-cultured with primary human lung microvascular endothelial cells (LMECs). We compared the susceptibility of LMECs to pandemic H1N1 virus and recent seasonal H1N1 and H3N2 viruses and assessed the associated pro-inflammatory responses. Despite the detection of IAV nucleoprotein in LMEC mono-cultures, there was no evidence for productive infection. In epithelial-endothelial co-cultures, abundant IAV infection of epithelial cells resulted in the breakdown of the epithelial barrier, but infection of LMECs was rarely detected. We observed a significantly higher secretion of pro-inflammatory cytokines in LMECs when co-cultured with IAV-infected epithelial cells than LMEC mono-cultures exposed to IAV. Taken together, our data show that LMECs are abortively infected by IAV but can fuel the inflammatory response.
. 2023 Apr 18;6(7):e202201837.
doi: 10.26508/lsa.202201837. Print 2023 Jul.
The pro-inflammatory response to influenza A virus infection is fueled by endothelial cells
Lisa Bauer[SUP] 1 [/SUP], Laurine C Rijsbergen[SUP] 2 [/SUP], Lonneke Leijten[SUP] 2 [/SUP], Feline Fw Benavides[SUP] 2 [/SUP], Danny Noack[SUP] 2 [/SUP], Mart M Lamers[SUP] 2 [/SUP], Bart L Haagmans[SUP] 2 [/SUP], Rory D de Vries[SUP] 2 [/SUP], Rik L de Swart[SUP] 2 [/SUP], Debby van Riel[SUP] 3 [/SUP]
Affiliations
- PMID: 37072183
- DOI: 10.26508/lsa.202201837
Abstract
Morbidity and mortality from influenza are associated with high levels of systemic inflammation. Endothelial cells play a key role in systemic inflammatory responses during severe influenza A virus (IAV) infections, despite being rarely infected in humans. How endothelial cells contribute to systemic inflammatory responses is unclear. Here, we developed a transwell system in which airway organoid-derived differentiated human lung epithelial cells were co-cultured with primary human lung microvascular endothelial cells (LMECs). We compared the susceptibility of LMECs to pandemic H1N1 virus and recent seasonal H1N1 and H3N2 viruses and assessed the associated pro-inflammatory responses. Despite the detection of IAV nucleoprotein in LMEC mono-cultures, there was no evidence for productive infection. In epithelial-endothelial co-cultures, abundant IAV infection of epithelial cells resulted in the breakdown of the epithelial barrier, but infection of LMECs was rarely detected. We observed a significantly higher secretion of pro-inflammatory cytokines in LMECs when co-cultured with IAV-infected epithelial cells than LMEC mono-cultures exposed to IAV. Taken together, our data show that LMECs are abortively infected by IAV but can fuel the inflammatory response.