Journal of the Korean Ophthalmological Society 1998;39(2):292-301.
Published online February 1, 1998.
Activation of Protein Tyrosine Kinase Pathway after Cat BRVO.
Hyung Chan Kim, Eugene De Juan
1Department of Ophthalmology, Kangnam Sacred Hear Hospital, Hallym University, Seoul, Korea.
2The Wilmer Eye Institute, Johns Hopkins University, Baltimore, MD, USA.
고양이망막분지정맥폐쇄후 Protein Tyrosine Kinase Pathway의 활성화
김형찬(Hyung Chan Kim) , (Eugene de Juan)
Abstract
To examine the effect of retinal branch vein occlusion (BRVO) on protein tyrosine phosphorylation, production of angiogenic growth factors, and activation of signal proteins in the tyrosine kinase pathways in the retina, BRVO was induced in cat retina by coagulation of retinal veins with diathermy. At 2 days, 1, 3, and 6 weeks after induction of BRVO, the retina was divided into 3 parts; a part within the distribution of the occluded vein [BRVO(IN)] or a part outside the distribution of the occluded vein [BRVO(OUT)], an prepared for western blot analysis. Overall, tyrosine-phosphorylated proteins were increased after BRVO, especially in BRVO(IN) at 2 days and 1 week. The vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (bFGF) were also increased in BRVO(IN) at 1 week and 2 days, respectively. The phospholipase Cgamma(PLCgamma) and mitogen-activated protein kinase (MAPK) were activated at these points. In this study, we concluded that the BRVO increased overall protein tyrosine phosphorylation in the cat retina in association with the increase of angiogenic growth factors (VEGF, bFGF) and activation of 2 signal proteins (PLCgamma and MAPK)in the tyrosine kinase pathways. These results suggest that the protein tyrosine phosphorylation may in part play an important role in mitogenesis of vascular endothelial cells and other retinal responses after BRVO.
Key Words: Angiogenic growth factor;BRVO;Protein tyrosine kinase pathway;Signal protein;Tyrosine phosphorylation


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