Glucocorticoid regulation of endothelial cell tight junction gene expression: Novel treatments for diabetic retinopathy

被引:75
作者
Felinski, EA [1 ]
Antonetti, DA
机构
[1] Penn State Univ, Coll Med, Dept Cellular & Mol Physiol, Hershey, PA 17033 USA
[2] Penn State Univ, Coll Med, Dept Cellular & Mol Physiol, Hershey, PA 17033 USA
[3] Penn State Univ, Coll Med, Dept Ophthalmol, Hershey, PA 17033 USA
关键词
diabetic retinopathy; glucocorticoids; tight junctions;
D O I
10.1080/02713680500263598
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Loss of blood-retinal barrier (BRB) integrity and vascular permeability characterizes diabetic retinopathy, and new therapies to reverse or prevent vascular permeability are needed to treat this debilitating disease. Glucocorticoids are currently under investigation for use as a local therapeutic treatment for diabetic retinopathy. This review examines the changes that occur to barrier properties in diabetic retinopathy and the potential to use glucocorticoids to restore vascular barrier properties in the retina. Glucocorticoids are useful in preserving the integrity of the blood-brain barrier in the treatment of brain tumors, and these steroids show similar effects on the retinal vasculature suggesting their potential usefulness in treating diabetic retinopathy. Recent progress has been made toward the goal of elucidating the precise mechanism underlying the protective effects of glucocorticoids on the retinal vasculature. Glucocorticoids may act by both suppressing inflammation and by directly affecting the endothelial cells by regulating phosphorylation, organization, and content of tight junction proteins. Further work will advance our understanding of glucocorticoid regulation of barrier properties allowing the ultimate goal of developing a specific and safe therapy to treat or prevent loss of the blood-neural barrier in a number of diseases, including brain tumors and diabetic retinopathy.
引用
收藏
页码:949 / 957
页数:9
相关论文
共 83 条
[1]   Diabetic retinopathy [J].
Aiello, LP ;
Gardner, TW ;
King, GL ;
Blankenship, G ;
Cavallerano, JD ;
Ferris, FL ;
Klein, R .
DIABETES CARE, 1998, 21 (01) :143-156
[2]   VASCULAR ENDOTHELIAL GROWTH-FACTOR IN OCULAR FLUID OF PATIENTS WITH DIABETIC-RETINOPATHY AND OTHER RETINAL DISORDERS [J].
AIELLO, LP ;
AVERY, RL ;
ARRIGG, PG ;
KEYT, BA ;
JAMPEL, HD ;
SHAH, ST ;
PASQUALE, LR ;
THIEME, H ;
IWAMOTO, MA ;
PARK, JE ;
NGUYEN, HV ;
AIELLO, LM ;
FERRARA, N ;
KING, GL .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (22) :1480-1487
[3]  
Antcliff R J, 1999, Semin Ophthalmol, V14, P223, DOI 10.3109/08820539909069541
[4]  
Antonetti D A, 1999, Semin Ophthalmol, V14, P240, DOI 10.3109/08820539909069543
[5]   Hydrocortisone decreases retinal endothelial cell water and solute flux coincident with increased content and decreased phosphorylation of occludin [J].
Antonetti, DA ;
Wolpert, EB ;
DeMaio, L ;
Harhaj, NS ;
Scaduto, RC .
JOURNAL OF NEUROCHEMISTRY, 2002, 80 (04) :667-677
[6]   Vascular endothelial growth factor induces rapid phosphorylation of tight junction proteins occludin and zonula occluden 1 - A potential mechanism for vascular permeability in diabetic retinopathy and tumors [J].
Antonetti, DA ;
Barber, AJ ;
Hollinger, LA ;
Wolpert, EB ;
Gardner, TW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (33) :23463-23467
[7]   Nuclear hormone receptors and gene expression [J].
Aranda, A ;
Pascual, A .
PHYSIOLOGICAL REVIEWS, 2001, 81 (03) :1269-1304
[8]   Lipid hydroperoxide stimulates retinal neovascularization in rabbit retina through expression of tumor necrosis factor-α, vascular endothelial growth factor and platelet-derived growth factor [J].
Armstrong D. ;
Ueda T. ;
Ueda T. ;
Aljada A. ;
Browne R. ;
Fukuda S. ;
Spengler R. ;
Chou R. ;
Hartnett M. ;
Buch P. ;
Dandona P. ;
Sasisekharan R. ;
Dorey C.K. .
Angiogenesis, 1998, 2 (1) :93-104
[9]  
Bakri SJ, 2003, OPHTHALMIC SUR LA IM, V34, P386
[10]   Molecular mechanisms of dissociative glucocorticoid activity [J].
Bamberger, CM ;
Schulte, HM .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2000, 30 :6-9