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Light-induced CREB phosphorylation and gene expression in rat retinal cells
K Yoshida1, J Imaki, H Matsuda
1Department of Ophthalmology, Hokkaido University School of Medicine, Sapporo, Japan.
Journal of Neurochemistry
|October 1, 1995
Summary
Light exposure triggers c-fos and somatostatin (SS) gene expression in rat retinal cells via CREB phosphorylation. This pathway involves Ca2+ channels and calmodulin kinase II in amacrine and ganglion cells.
Area of Science:
- Neuroscience
- Molecular Biology
- Cell Biology
Background:
- Light-induced gene expression is crucial for retinal function.
- The c-fos and somatostatin (SS) genes are implicated in neuronal responses.
- Cyclic AMP response elements (CRE) in gene promoters suggest a role for CRE-binding protein (CREB).
Purpose of the Study:
- To investigate the signaling pathway for light-induced c-fos and SS expression in rat retinal cells.
- To determine the role of CREB phosphorylation in this light-induced pathway.
Main Methods:
- Utilized flashing light stimuli on rat retinal cells.
- Administered the L-type Ca2+ channel activator Bay K 8644.
- Employed phospho-CREB-specific antibodies and anti-calmodulin kinase II (CaM kinase II) antibodies for immunofluorescence.
- Analyzed mRNA expression of c-fos and SS.
Main Results:
- Flashing light induced c-fos and SS mRNA in the inner nuclear and ganglion cell layers.
- Both light and Bay K 8644 induced CREB phosphorylation in amacrine and ganglion cells.
- Phosphorylated CREB (Ser133) and CaM kinase II colocalized in the neural retina.
Conclusions:
- Light-induced c-fos and SS expression in rat retinal cells is mediated by CREB phosphorylation.
- L-type Ca2+ channels and CaM kinase II are involved in this signaling pathway.
- This study elucidates a key molecular mechanism in retinal light response.