Nestin Expression in the Adult Mouse Retina with Pharmaceutically Induced Retinal Degeneration.
Chan Hee MoonHeeyoon ChoYoon Kyung KimTae Kwann ParkPublished in: Journal of Korean medical science (2017)
The present study investigated the temporal pattern and cellular localization of nestin in the adult mouse retina with pharmaceutically induced retinal degeneration using N-methyl-N-nitrosourea (MNU). After a single intraperitoneal injection of MNU in 8-week-old C57BL/6 mice, the animals were sacrificed at 1, 3, 5, 7, and 21 days (n = 6, in each stage). The eyes were examined by means of immunohistochemical tests using nestin, ionized calcium-binding adaptor molecule (Iba-1), CD11b, F4/80, and glial fibrillary acidic protein (GFAP). Western blot analysis and manual cell counting were performed for quantification. Nestin expression was increased after MNU administration. Nestin+/Iba-1+ cells were migrated into outer nuclear layer (ONL) and peaked at day 3 post injection (PI). Nestin+/CD11b+ cells were also mainly identified in ONL at day 3 PI and peaked at day 5. Nestin+/F4/80+ cells were shown in the subretinal space and peaked at day 3 PI. Nestin+/GFAP+ cells were distinctly increased at day 1 PI and peaked at day 5 PI. The up-regulation of nestin expression after MNU administration in adult mouse retinal microglia, and monocyte/macrophage suggests that when retinal degeneration progresses, these cells may revert to a more developmentally immature state. Müller cells also showed reactive gliosis and differentiational changes.
Keyphrases
- induced apoptosis
- cell cycle arrest
- optical coherence tomography
- diabetic retinopathy
- poor prognosis
- endoplasmic reticulum stress
- signaling pathway
- adipose tissue
- binding protein
- single cell
- inflammatory response
- oxidative stress
- young adults
- mass spectrometry
- small molecule
- immune response
- cell proliferation
- transcription factor
- ultrasound guided
- cell therapy
- high glucose
- data analysis
- dna binding