Evidence for the involvement of interleukin-1α during development of experimental cytomegalovirus retinitis in immunosuppressed mice

Cytokine. 2021 Aug:144:155596. doi: 10.1016/j.cyto.2021.155596. Epub 2021 May 30.

Abstract

Interleukin-1α (IL-1α) is an alarmin involved in the recruitment of macrophages and neutrophils during tissue inflammation. IL-1α can undergo cleavage by proteases, such as calpain-1, that enhances IL-1α binding to its receptor, although proteolytic cleavage is not necessary for biological activity. Macrophages and neutrophils are involved in the retinal inflammation associated with development of AIDS-related human cytomegalovirus (HCMV) retinitis. We therefore performed studies to test the hypothesis that IL-1α gene expression is stimulated intraocularly during retinitis development using two mouse models of murine cytomegalovirus (MCMV) retinitis that differ in method of immunosuppression, one by retrovirus-induced immunosuppression (MAIDS) and the other by corticosteroid-induced immunosuppression. MCMV-infected eyes of groups of retinitis-susceptible mice with MAIDS of 10 weeks duration (MAIDS-10 mice) and retinitis-susceptible corticosteroid-treated mice showed significant stimulation of IL-1α mRNA. Western blot analysis confirmed IL-1α protein production within the MCMV-infected eyes of MAIDS-10 mice. Whereas significant intraocular calpain-1 mRNA and protein production were also observed within MCMV-infected eyes of MAIDS-10 mice, the MCMV-infected eyes of retinitis-susceptible corticosteroid-treated mice showed a pattern of mRNA synthesis equivalent to that found within the MCMV-infected eyes of healthy mice that fail to develop retinitis. Our findings suggest a role for the alarmin IL-1α in the pathogenesis of MCMV retinitis in immunosuppressed mice. These findings may extend to the pathogenesis of HCMV retinitis in patients with AIDS or other forms of immunosuppression.

Keywords: AIDS; Calpain-1; Corticosteroid; Cytomegalovirus; Interleukin-1α; Retinitis.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Cytomegalovirus Retinitis / immunology*
  • Disease Models, Animal
  • Female
  • Immune Tolerance / immunology
  • Immunosuppression Therapy / methods
  • Interleukin-1alpha / immunology*
  • Macrophages / immunology
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Murine Acquired Immunodeficiency Syndrome / immunology*
  • Muromegalovirus / immunology*
  • RNA, Messenger / immunology
  • Retina / immunology*

Substances

  • Interleukin-1alpha
  • RNA, Messenger