PUBLICATION

Development and Use of Retinal Pigmented Epithelial Cell Line from Zebrafish (Danio rerio) for Evaluating the Toxicity of Ultraviolet-B

Authors
Nambi, K.S., Abdul Majeed, S., Taju, G., Sivasubbu, S., Sundar Raj, N., Madan, N., Sahul Hameed, A.S.
ID
ZDB-PUB-141218-6
Date
2015
Source
Zebrafish   12(1): 21-32 (Journal)
Registered Authors
Sivasubbu, Sridhar
Keywords
none
MeSH Terms
  • Animals
  • Cell Survival/radiation effects*
  • Cells, Cultured/radiation effects
  • Retinal Pigment Epithelium/cytology
  • Retinal Pigment Epithelium/radiation effects
  • Toxicity Tests/methods*
  • Ultraviolet Rays/adverse effects*
  • Zebrafish*
PubMed
25517103 Full text @ Zebrafish
Abstract
Abstract Danio rerio retinal pigmented epithelial (DrRPE) cell line, derived from the RPE tissue, was established and characterized. The cells were able to grow at a wide range of temperatures from 25°C to 32°C in Leibovitz's L-15 medium. The DrRPE cell line consists of epithelial cells with a diameter of 15-19 μm. The cell line was characterized by mitochondrial 12S rRNA gene, immunocytochemical analysis, and karyotyping. DrRPE cells treated with 10 μM of all-trans-retinol for 24 h readily formed lipid droplets. DrRPE cells were irradiated with narrowband ultraviolet-B (UV-B) radiation at different time periods of 0, 10, 20, and 40 min. The cells were subsequently examined for changes in morphology, cell viability, phagocytotic activity, mitochondrial distribution, nuclei morphology, generation of reactive oxygen species, and expression of apoptotic-related genes p53 and Cas3 by quantitative polymerase chain reaction. The results demonstrate that UV-B radiation can cause a considerable decrease in DrRPE cell viability as well as in phagocytotic activity. In addition, the results demonstrate that UV-B radiation can induce the degradation of mitochondria and DNA in cultured DrRPE cells.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping