Polyinosinic: Polycytidylic Acid and Murine Cytomegalovirus Modulate Expression of Murine IL-10 and IL-21 in White Adipose Tissue.

Viruses

Experimental Therapeutics Laboratory, UniSA Cancer Research Institute, Clinical and Health Sciences, University of South Australia, Adelaide 5000, Australia.

Published: May 2020

AI Article Synopsis

  • * Researchers used in vivo and ex vivo methods to assess how viral stimuli—polyinosinic:polycytidylic acid (poly(I:C)) and murine cytomegalovirus (MCMV)—affect IL-10 production in WAT.
  • * Results showed that while poly(I:C) boosts IL-10 and IL-21 levels, MCMV infections lead to lower IL-10 and fewer regulatory B-cells, indicating differing immune responses to these viral stimuli

Article Abstract

White adipose tissue (WAT) produces interleukin-10 and other immune suppressors in response to pathogen-associated molecular patterns (PAMPs). It also homes a subset of B-cells specialized in the production of IL-10, referred to as regulatory B-cells. We investigated whether viral stimuli, polyinosinic: polycytidylic acid (poly(I:C)) or whole replicative murine cytomegalovirus (MCMV), could stimulate the expression of IL-10 in murine WAT using in vivo and ex vivo approaches. Our results showed that in vivo responses to systemic administration of poly(I:C) resulted in high levels of endogenously-produced IL-10 and IL-21 in WAT. In ex vivo WAT explants, a subset of B-cells increased their endogenous IL-10 expression in response to poly(I:C). Finally, MCMV replication in WAT explants resulted in decreased IL-10 levels, opposite to the effect seen with poly(I:C). Moreover, downregulation of IL-10 correlated with relatively lower number of Bregs. To our knowledge, this is the first report of IL-10 expression by WAT and WAT-associated B-cells in response to viral stimuli.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7290755PMC
http://dx.doi.org/10.3390/v12050569DOI Listing

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