Differential response of Müller cells and microglia in a mouse retinal detachment model and its implications in detached and non-detached regions

Seung Hee Lee, Yong Soo Park, Sun Sook Paik, In Beom Kim

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

Retinal detachment (RD) is a sight-threatening condition, leading to photoreceptor cell death; however, only a few studies provide insight into its effects on the entire retinal region. We examined the spatiotemporal changes in glial responses in a mouse RD model. In electroretinogra-phy, a-and b-waves were reduced in a time-dependent manner. Hematoxylin and eosin staining revealed a gradual decrease in the outer nuclear layer throughout the retinal region. Terminal de-oxynucleotidyltransferase dUTP nick end labeling (TUNEL) assay showed that TUNEL-positive photoreceptors increased 5 days after RD and decreased by 14 days. Glial response was evaluated by immunohistochemistry using antibodies against glial fibrillary acidic protein (GFAP, Müller glial marker) and Iba-1 (microglial marker) and osteopontin (OPN, activated microglial marker). GFAP immunoreactivity increased after 7 days in complete RD, and was retained for 14 days. OPN expression increased in microglial cells 3–7 days after RD, and decreased by 14 days in the detached and border regions. Although OPN was not expressed in the intact region, morphologically activated microglial cells were observed. These retinal glial cell responses and photoreceptor degeneration in the border and intact regions suggest that the effects of RD in the border and intact retinal regions need to be understood further.

Original languageEnglish
Article number1972
JournalCells
Volume10
Issue number8
DOIs
StatePublished - Aug 2021

Bibliographical note

Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.

Keywords

  • GFAP
  • Microglia
  • Müller cells
  • Osteopontin
  • Retinal detachment

Fingerprint

Dive into the research topics of 'Differential response of Müller cells and microglia in a mouse retinal detachment model and its implications in detached and non-detached regions'. Together they form a unique fingerprint.

Cite this