• FluTrackers.com Inc. does not provide medical advice. Information on this web site is collected from various internet resources, and the FluTrackers board of directors makes no warranty to the safety, efficacy, correctness or completeness of the information posted on this site by any author or poster. The information collated here is for instructional and/or discussion purposes only and is NOT intended to diagnose or treat any disease, illness, or other medical condition. Every individual reader or poster should seek advice from their personal physician/healthcare practitioner before considering or using any interventions that are discussed on this website. By continuing to access this website you agree to consult your personal physican before using any interventions posted on this website, and you agree to hold harmless FluTrackers.com Inc., the board of directors, the members, and all authors and posters for any effects from use of any medication, supplement, vitamin or other substance, device, intervention, etc. mentioned in posts on this website, or other internet venues referenced in posts on this website.
  • We are not asking for any donations. Do not donate to any entity who says they are raising funds for us.

Cell Death Dis . SARS-CoV-2 infection induces persistent adipose tissue damage in aged golden Syrian hamsters

tetano

Editor, Senior Moderator
Cell Death Dis


. 2023 Feb 1;14(2):75.
doi: 10.1038/s41419-023-05574-w.
SARS-CoV-2 infection induces persistent adipose tissue damage in aged golden Syrian hamsters


Gemma Bogard[SUP] #[/SUP][SUP] 1 [/SUP], Johanna Barthelemy[SUP] #[/SUP][SUP] 1 [/SUP], Aline Hantute-Ghesquier[SUP] 2 [/SUP], Valentin Sencio[SUP] 1 [/SUP], Patricia Brito-Rodrigues[SUP] 1 [/SUP], Karin Séron[SUP] 1 [/SUP], Cyril Robil[SUP] 1 [/SUP], Anne Flourens[SUP] 2 [/SUP], Florence Pinet[SUP] 3 [/SUP], Delphine Eberlé[SUP] 4 [/SUP], François Trottein[SUP] 1 [/SUP], Martine Duterque-Coquillaud[SUP] 2 [/SUP], Isabelle Wolowczuk[SUP] 5 [/SUP]



Affiliations

Abstract

Coronavirus disease 2019 (COVID-19, caused by severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2)) is primarily a respiratory illness. However, various extrapulmonary manifestations have been reported in patients with severe forms of COVID-19. Notably, SARS-CoV-2 was shown to directly trigger white adipose tissue (WAT) dysfunction, which in turn drives insulin resistance, dyslipidemia, and other adverse outcomes in patients with COVID-19. Although advanced age is the greatest risk factor for COVID-19 severity, published data on the impact of SARS-CoV-2 infection on WAT in aged individuals are scarce. Here, we characterized the response of subcutaneous and visceral WAT depots to SARS-CoV-2 infection in young adult and aged golden hamsters. In both age groups, infection was associated with a decrease in adipocyte size in the two WAT depots; this effect was partly due to changes in tissue's lipid metabolism and persisted for longer in aged hamsters than in young-adult hamsters. In contrast, only the subcutaneous WAT depot contained crown-like structures (CLSs) in which dead adipocytes were surrounded by SARS-CoV-2-infected macrophages, some of them forming syncytial multinucleated cells. Importantly, older age predisposed to a unique manifestation of viral disease in the subcutaneous WAT depot during SARS-CoV-2 infection; the persistence of very large CLSs was indicative of an age-associated defect in the clearance of dead adipocytes by macrophages. Moreover, we uncovered age-related differences in plasma lipid profiles during SARS-CoV-2 infection. These data suggest that the WAT's abnormal response to SARS-CoV-2 infection may contribute to the greater severity of COVID-19 observed in elderly patients.
 
Back
Top Bottom