Suppression of microglial activation is neuroprotective in a mouse model of human retinitis pigmentosa

Bo Peng, Jia Xiao, Ke Wang, Kwok Fai So, George L. Tipoe, Bin Lin

Research output: Journal article publicationJournal articleAcademic researchpeer-review

181 Citations (Scopus)


Retinitis pigmentosa (RP) is a photoreceptor-degenerative disease caused by various mutations and is characterized by death of rod photoreceptor cell followed by gradual death of cone photoreceptors. The molecular mechanisms that lead to rod and cone death are not yet fully understood. Neuroinflammation contributes to the progression of many chronic neurodegenerative disorders. However, it remains to be determined how microglia contribute to photoreceptor disruption in RP. In this study, we explored the role of microglia as a contributor to photoreceptor degeneration in the rd10 mouse model of RP. First,wedemonstrated that microglia activation was an early alteration in RP retinas. Inhibition of microglia activation by minocycline reduced photoreceptor apoptosis and significantly improved retinal structure and function and visual behavior in rd10 mice. Second, we identified that minocycline exerted its neuroprotective effects through both anti-inflammatory and anti-apoptotic mechanisms. Third, we found that Cx3cr1 deficiency dysregulated microglia activation and subsequently resulted in increased photoreceptor vulnerability in rd10 mice, suggesting that the Cx3cl1/Cx3cr1 signaling pathway might protect against microglia neurotoxicity. We concluded that suppression of neuroinflammatory responses could be a potential treatment strategy aimed at improving photoreceptor survival in human RP.
Original languageEnglish
Pages (from-to)8139-8150
Number of pages12
JournalJournal of Neuroscience
Issue number24
Publication statusPublished - 1 Jan 2014
Externally publishedYes


  • Cx3cr1
  • Microglia
  • Minocycline
  • Photoreceptor degeneration
  • Rd10 mice

ASJC Scopus subject areas

  • Neuroscience(all)


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