tetano
Editor, Senior Moderator
Front Immunol
. 2024 Jun 7:15:1397990.
doi: 10.3389/fimmu.2024.1397990. eCollection 2024. Aging is associated with an insufficient early inflammatory response of lung endothelial cells in SARS-CoV-2 infection
Saravanan Subramaniam[SUP] 1 [/SUP], Devin Kenney[SUP] 2 3 [/SUP], Archana Jayaraman[SUP] 1 [/SUP], Aoife Kateri O'Connell[SUP] 2 4 [/SUP], Sarah Walachowski[SUP] 1 5 [/SUP], Paige Montanaro[SUP] 3 4 [/SUP], Christoph Reinhardt[SUP] 5 6 [/SUP], Giuseppe Colucci[SUP] 7 8 [/SUP], Nicholas A Crossland[SUP] 2 3 4 [/SUP], Florian Douam[SUP] 2 3 [/SUP], Markus Bosmann[SUP] 1 2 5 [/SUP]
Affiliations
Advanced age is associated with an increased susceptibility to Coronavirus Disease (COVID)-19 and more severe outcomes, although the underlying mechanisms are understudied. The lung endothelium is located next to infected epithelial cells and bystander inflammation may contribute to thromboinflammation and COVID-19-associated coagulopathy. Here, we investigated age-associated SARS-CoV-2 pathogenesis and endothelial inflammatory responses using humanized K18-hACE2 mice. Survival was reduced to 20% in aged mice (85-112 weeks) versus 50% in young mice (12-15 weeks) at 10 days post infection (dpi). Bulk RNA-sequencing of endothelial cells from mock and infected mice at 2dpi of both age groups (aged: 72-85 weeks; young: 15 weeks) showed substantially lower significant differentially regulated genes in infected aged mice than in young mice (712 versus 2294 genes). Viral recognition and anti-viral pathways such as RIG-I-like receptor signaling, NOD-like receptor signaling and interferon signaling were regulated in response to SARS-CoV-2. Young mice showed several fold higher interferon responses (Ifitm3, Ifit1, Isg15, Stat1) and interferon-induced chemokines (Cxcl10 and Cxcl11) than aged mice. Endothelial cells from infected young mice displayed elevated expression of chemokines (Cxcl9, Ccl2) and leukocyte adhesion markers (Icam1) underscoring that inflammation of lung endothelium during infection could facilitate leukocyte adhesion and thromboinflammation. TREM1 and acute phase response signaling were particularly prominent in endothelial cells from infected young mice. Immunohistochemistry was unable to detect viral protein in pulmonary endothelium. In conclusion, our data demonstrate that the early host response of the endothelium to SARS-CoV-2 infection declines with aging, which could be a potential contributor to disease severity.
Keywords: cytokines; host-pathogen interaction; inflammation; pattern recognition receptors; thromboinflammation.
. 2024 Jun 7:15:1397990.
doi: 10.3389/fimmu.2024.1397990. eCollection 2024. Aging is associated with an insufficient early inflammatory response of lung endothelial cells in SARS-CoV-2 infection
Saravanan Subramaniam[SUP] 1 [/SUP], Devin Kenney[SUP] 2 3 [/SUP], Archana Jayaraman[SUP] 1 [/SUP], Aoife Kateri O'Connell[SUP] 2 4 [/SUP], Sarah Walachowski[SUP] 1 5 [/SUP], Paige Montanaro[SUP] 3 4 [/SUP], Christoph Reinhardt[SUP] 5 6 [/SUP], Giuseppe Colucci[SUP] 7 8 [/SUP], Nicholas A Crossland[SUP] 2 3 4 [/SUP], Florian Douam[SUP] 2 3 [/SUP], Markus Bosmann[SUP] 1 2 5 [/SUP]
Affiliations
- PMID: 38911865
- PMCID: PMC11190167
- DOI: 10.3389/fimmu.2024.1397990
Advanced age is associated with an increased susceptibility to Coronavirus Disease (COVID)-19 and more severe outcomes, although the underlying mechanisms are understudied. The lung endothelium is located next to infected epithelial cells and bystander inflammation may contribute to thromboinflammation and COVID-19-associated coagulopathy. Here, we investigated age-associated SARS-CoV-2 pathogenesis and endothelial inflammatory responses using humanized K18-hACE2 mice. Survival was reduced to 20% in aged mice (85-112 weeks) versus 50% in young mice (12-15 weeks) at 10 days post infection (dpi). Bulk RNA-sequencing of endothelial cells from mock and infected mice at 2dpi of both age groups (aged: 72-85 weeks; young: 15 weeks) showed substantially lower significant differentially regulated genes in infected aged mice than in young mice (712 versus 2294 genes). Viral recognition and anti-viral pathways such as RIG-I-like receptor signaling, NOD-like receptor signaling and interferon signaling were regulated in response to SARS-CoV-2. Young mice showed several fold higher interferon responses (Ifitm3, Ifit1, Isg15, Stat1) and interferon-induced chemokines (Cxcl10 and Cxcl11) than aged mice. Endothelial cells from infected young mice displayed elevated expression of chemokines (Cxcl9, Ccl2) and leukocyte adhesion markers (Icam1) underscoring that inflammation of lung endothelium during infection could facilitate leukocyte adhesion and thromboinflammation. TREM1 and acute phase response signaling were particularly prominent in endothelial cells from infected young mice. Immunohistochemistry was unable to detect viral protein in pulmonary endothelium. In conclusion, our data demonstrate that the early host response of the endothelium to SARS-CoV-2 infection declines with aging, which could be a potential contributor to disease severity.
Keywords: cytokines; host-pathogen interaction; inflammation; pattern recognition receptors; thromboinflammation.