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Neuroprotective Mechanisms of Ciliary Neurotrophic Factor in Retinal Ganglion Cells: Insights from Microarray Analysis

Authors
 Seungyeon Lee  ;  Jin-Ok Choi  ;  Ahreum Hwang  ;  Chan Yun Kim  ;  Kwanghyun Lee 
Citation
 Korean Journal of Ophthalmology, Vol.39(2) : 125-133, 2025-04 
Journal Title
Korean Journal of Ophthalmology
ISSN
 1011-8942 
Issue Date
2025-04
MeSH
Animals ; Animals, Newborn ; Cells, Cultured ; Ciliary Neurotrophic Factor* / genetics ; Ciliary Neurotrophic Factor* / pharmacology ; Disease Models, Animal ; Gene Expression Profiling ; Gene Expression Regulation* ; Microarray Analysis ; Oligonucleotide Array Sequence Analysis ; Rats ; Rats, Sprague-Dawley ; Retinal Ganglion Cells* / drug effects ; Retinal Ganglion Cells* / metabolism ; Retinal Ganglion Cells* / pathology
Keywords
Ciliary neurotrophic factor ; Microarray analysis ; Retinal ganglion cells
Abstract
Purpose: This study investigated the changes in gene expression in retinal ganglion cells (RGCs) following ciliary neurotrophic factor (CNTF) treatment to elucidate the underlying mechanisms contributing to its neuroprotective effects.

Methods: RGCs isolated from Sprague-Dawley rat pups were treated with recombinant CNTF. Gene expression was analyzed via microarray. Differentially expressed genes (DEGs) were defined as those with a fold change greater than 2 or less than -2. The DEGs were further explored using Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses.

Results: Our analysis identified 71 upregulated and 58 downregulated genes. A2m exhibited the highest increase, with a fold change of 4.97, whereas Rho displayed the most significant decrease in expression, with a fold change of -6.38. GO and KEGG pathway analyses revealed substantial involvement in sensory organ development and the phototransduction pathway.

Conclusions: This study provides new insights into the impact of CNTF on gene expression in RGCs, suggesting broader neuroprotective mechanisms that could inform future therapeutic strategies for retinal degenerative diseases. Our findings emphasize the importance of further investigation into the complex gene network responses to CNTF treatment.
Files in This Item:
T202507697.pdf Download
DOI
10.3341/kjo.2024.0148
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Ophthalmology (안과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Chan Yun(김찬윤) ORCID logo https://orcid.org/0000-0002-8373-9999
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/209388
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