4.6 Article

Microglial Activation Is Associated With Vasoprotection in a Rat Model of Inflammatory Retinal Vasoregression

Journal

FRONTIERS IN PHYSIOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fphys.2021.660164

Keywords

retinopathy; pericyte; microglia; vasoregression; clodronate

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Funding

  1. Deutsche Forschungsgemeinschaft (DFG) within the International Research Training Group 1874 Diabetic Microvascular Complications [Fe 969/2-1, HA 1755/10-1]
  2. European Foundation for the Study of Diabetes (EFSD)

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Vascular dysfunction and vasoregression are characteristics of various inflammatory central nervous system disorders and inflammation-related retinal diseases. Activation of microglia and the humoral innate immune system play contributing roles. In this study, clodronate treatment led to an increase in activated CD74(+) microglia and prevented acellular capillaries and pericyte loss, indicating a shift towards induction of pleiotropic protective pathways supporting vasoprotection in neurovascular retinal diseases.
Vascular dysfunction and vasoregression are hallmarks of a variety of inflammatory central nervous system disorders and inflammation-related retinal diseases like diabetic retinopathy. Activation of microglia and the humoral innate immune system are contributing factors. Anti-inflammatory approaches have been proposed as therapies for neurovascular diseases, which include the modulation of microglial activation. The present study aimed at investigating the effects of microglial activation by clodronate-coated liposomes on vasoregression in a model of retinal degeneration. Clodronate treatment over 5 weeks led to an increase in activated CD74(+) microglia and completely prevented acellular capillaries and pericyte loss. Gene expression analyses indicated that vasoprotection was due to the induction of vasoprotective factors such as Egr1, Stat3, and Ahr while expression of pro-inflammatory genes remained unchanged. We concluded that activated microglia led to a shift toward induction of pleiotropic protective pathways supporting vasoprotection in neurovascular retinal diseases.

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