Frontiers in Immunology (Mar 2021)

Anti-Inflammatory (M2) Response Is Induced by a sp2-Iminosugar Glycolipid Sulfoxide in Diabetic Retinopathy

  • Fátima Cano-Cano,
  • Fátima Cano-Cano,
  • Elena Alcalde-Estévez,
  • Laura Gómez-Jaramillo,
  • Laura Gómez-Jaramillo,
  • Marta Iturregui,
  • Marta Iturregui,
  • Elena M. Sánchez-Fernández,
  • José M. García Fernández,
  • Carmen Ortiz Mellet,
  • Antonio Campos-Caro,
  • Antonio Campos-Caro,
  • Cristina López-Tinoco,
  • Manuel Aguilar-Diosdado,
  • Manuel Aguilar-Diosdado,
  • Ángela M. Valverde,
  • Ángela M. Valverde,
  • Ana I. Arroba,
  • Ana I. Arroba

DOI
https://doi.org/10.3389/fimmu.2021.632132
Journal volume & issue
Vol. 12

Abstract

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Diabetic retinopathy (DR) is one of the most common complications of Diabetes Mellitus (DM) and is directly associated with inflammatory processes. Currently, neuro-inflammation is considered an early event in DR and proceeds via microglia polarization. A hallmark of DR is the presence of retinal reactive gliosis. Here we report the beneficial effect of (SS,1R)-1-docecylsulfiny-5N,6O-oxomethylidenenojirimycin ((Ss)-DS-ONJ), a member of the sp2-iminosugar glycolipid (sp2-IGL) family, by decreasing iNOS and inflammasome activation in Bv.2 microglial cells exposed to pro-inflammatory stimuli. Moreover, pretreatment with (Ss)-DS-ONJ increased Heme-oxygenase (HO)-1 as well as interleukin 10 (IL10) expression in LPS-stimulated microglial cells, thereby promoting M2 (anti-inflammatory) response by the induction of Arginase-1. The results strongly suggest that this is the likely molecular mechanism involved in the anti-inflammatory effects of (SS)-DS-ONJ in microglia. (SS)-DS-ONJ further reduced gliosis in retinal explants from type 1 diabetic BB rats, which is consistent with the enhanced M2 response. In conclusion, targeting microglia polarization dynamics in M2 status by compounds with anti-inflammatory activities offers promising therapeutic interventions at early stages of DR.

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