INVOLVEMENT OF THE PROTEIN KINASE PATHWAY IN MELANIN SYNTHESIS BY CHICK RETINAL PIGMENT EPITHELIAL CELLS
✍ Scribed by Hiroko Kishi; Hiromu K Mishima; Uki Yamashita
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 107 KB
- Volume
- 24
- Category
- Article
- ISSN
- 1065-6995
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Protein kinases are involved in a variety of cellular functions and cell proliferation in eyes. We have explored the involvement of protein kinase C (PKC) in cell proliferation and melanin synthesis by chick retinal pigment epithelial (RPE) cells in vitro. This was achieved by incubation of confluent RPE cells with known inhibitors of protein kinase, H‐7, W‐7, H‐8, and staurosporine. Chick RPE cells were cultured in the presence or absence of the protein kinase inhibitors for a 10‐day period. Effects of the inhibitors on cell proliferation and melanin synthesis, as an indication of cell differentiation, were assessed by counting the number of surviving cells and by measuring the melanin content in the cells, respectively. H‐7, W‐7, and staurosporine inhibited cell proliferation and increased melanin synthesis in a concentration‐dependent manner during culture; however, H‐8 did not produce these cellular effects. These findings indicate that PKC and calcium/calmodulin‐dependent kinase pathways are involved in the proliferation and differentiation of chick RPE cells.
📜 SIMILAR VOLUMES
## Abstract Vascular endothelial growth factor (VEGF) is a major agent in choroidal and retinal neovascularization, events associated with age‐related macular degeneration (AMD) and diabetic retinopathy. Retinal pigment epithelium (RPE), strategically located between retina and choroid, plays a cri
## Abstract Extracellular acidosis (EA) regulates Heme Oxygenase‐1 (HO‐1) expression in vascular smooth muscle cells via transcriptional and posttranscriptional mechanisms but the signaling pathways involved are not known. We examined the role of Mitogen‐Activated Protein Kinase (MAPK) pathways in