tetano
Editor, Senior Moderator
Sci Rep
. 2024 Aug 24;14(1):19703.
doi: 10.1038/s41598-024-70612-2. Premature aging effects on COVID-19 pathogenesis: new insights from mouse models
Wu Haoyu[SUP] #[/SUP][SUP] 1 [/SUP], Liu Meiqin[SUP] #[/SUP][SUP] 2 3 [/SUP], Sun Jiaoyang[SUP] 4 [/SUP], Hong Guangliang[SUP] 4 [/SUP], Lin Haofeng[SUP] 2 [/SUP], Chen Pan[SUP] 5 [/SUP], Quan Xiongzhi[SUP] 5 [/SUP], Wu Kaixin[SUP] 6 [/SUP], Hu Mingli[SUP] 5 [/SUP], Yang Xuejie[SUP] 5 [/SUP], Ingo Lämmermann[SUP] 7 [/SUP], Johannes Grillari[SUP] 8 9 10 [/SUP], Shi Zhengli[SUP] 2 [/SUP], Chen Jiekai[SUP] 11 12 [/SUP], Wu Guangming[SUP] 13 14 [/SUP]
Affiliations
Aging is identified as a significant risk factor for severe coronavirus disease-2019 (COVID-19), often resulting in profound lung damage and mortality. Yet, the biological relationship between aging, aging-related comorbidities, and COVID-19 remains incompletely understood. This study aimed to elucidate the age-related COVID19 pathogenesis using an Hutchinson-Gilford progeria syndrome (HGPS) mouse model, a premature aging disease model, with humanized ACE2 receptors. Pathological features were compared between young, aged, and HGPS hACE2 mice following SARS-CoV-2 challenge. We demonstrated that young mice display robust interferon response and antiviral activity, whereas this response is attenuated in aged mice. Viral infection in aged mice results in severe respiratory tract hemorrhage, likely contributing a higher mortality rate. In contrast, HGPS hACE2 mice exhibit milder disease manifestations characterized by minor immune cell infiltration and dysregulation of multiple metabolic processes. Comprehensive transcriptome analysis revealed both shared and unique gene expression dynamics among different mouse groups. Collectively, our studies evaluated the impact of SARS-CoV-2 infection on progeroid syndromes using a HGPS hACE2 mouse model, which holds promise as a useful tool for investigating COVID-19 pathogenesis in individuals with premature aging.
Keywords: Aging; HGPS; Premature aging; Progeria; SARS-CoV-2; hACE2 mice.
. 2024 Aug 24;14(1):19703.
doi: 10.1038/s41598-024-70612-2. Premature aging effects on COVID-19 pathogenesis: new insights from mouse models
Wu Haoyu[SUP] #[/SUP][SUP] 1 [/SUP], Liu Meiqin[SUP] #[/SUP][SUP] 2 3 [/SUP], Sun Jiaoyang[SUP] 4 [/SUP], Hong Guangliang[SUP] 4 [/SUP], Lin Haofeng[SUP] 2 [/SUP], Chen Pan[SUP] 5 [/SUP], Quan Xiongzhi[SUP] 5 [/SUP], Wu Kaixin[SUP] 6 [/SUP], Hu Mingli[SUP] 5 [/SUP], Yang Xuejie[SUP] 5 [/SUP], Ingo Lämmermann[SUP] 7 [/SUP], Johannes Grillari[SUP] 8 9 10 [/SUP], Shi Zhengli[SUP] 2 [/SUP], Chen Jiekai[SUP] 11 12 [/SUP], Wu Guangming[SUP] 13 14 [/SUP]
Affiliations
- PMID: 39181932
- DOI: 10.1038/s41598-024-70612-2
Aging is identified as a significant risk factor for severe coronavirus disease-2019 (COVID-19), often resulting in profound lung damage and mortality. Yet, the biological relationship between aging, aging-related comorbidities, and COVID-19 remains incompletely understood. This study aimed to elucidate the age-related COVID19 pathogenesis using an Hutchinson-Gilford progeria syndrome (HGPS) mouse model, a premature aging disease model, with humanized ACE2 receptors. Pathological features were compared between young, aged, and HGPS hACE2 mice following SARS-CoV-2 challenge. We demonstrated that young mice display robust interferon response and antiviral activity, whereas this response is attenuated in aged mice. Viral infection in aged mice results in severe respiratory tract hemorrhage, likely contributing a higher mortality rate. In contrast, HGPS hACE2 mice exhibit milder disease manifestations characterized by minor immune cell infiltration and dysregulation of multiple metabolic processes. Comprehensive transcriptome analysis revealed both shared and unique gene expression dynamics among different mouse groups. Collectively, our studies evaluated the impact of SARS-CoV-2 infection on progeroid syndromes using a HGPS hACE2 mouse model, which holds promise as a useful tool for investigating COVID-19 pathogenesis in individuals with premature aging.
Keywords: Aging; HGPS; Premature aging; Progeria; SARS-CoV-2; hACE2 mice.