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Bone Morphogenetic Proteins and Diabetic Retinopathy
被引:12
|作者:
Elmasry, Khaled
[1
,2
,3
]
Habib, Samar
[4
,5
]
Moustafa, Mohamed
[2
,6
]
Al-Shabrawey, Mohamed
[1
,2
,6
]
机构:
[1] Augusta Univ, Med Coll Georgia, Dept Cellular Biol & Anat, Augusta, GA 30912 USA
[2] Augusta Univ, Culver Vis Discovery Inst, Augusta, GA 30912 USA
[3] Mansoura Univ, Mansoura Fac Med, Dept Anat, Dakahlia Governorate 35516, Egypt
[4] Mansoura Univ, Mansoura Fac Med, Dept Med Parasitol, Dakahlia Governorate 35516, Egypt
[5] Augusta Univ, Dept Obstet & Gynecol, Med Coll Georgia, Augusta, GA 30912 USA
[6] Augusta Univ, Dept Oral Biol & Diagnost Sci, Dent Coll Georgia, Augusta, GA 30912 USA
关键词:
bone morphognetic proteins;
BMP2;
BMP4;
diabetic retinopathy;
age-related macular degeneration;
D O I:
10.3390/biom11040593
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Bone morphogenetic proteins (BMPs) play an important role in bone formation and repair. Recent studies underscored their essential role in the normal development of several organs and vascular homeostasis in health and diseases. Elevated levels of BMPs have been linked to the development of cardiovascular complications of diabetes mellitus. However, their particular role in the pathogenesis of microvascular dysfunction associated with diabetic retinopathy (DR) is still under-investigated. Accumulated evidence from our and others' studies suggests the involvement of BMP signaling in retinal inflammation, hyperpermeability and pathological neovascularization in DR and age-related macular degeneration (AMD). Therefore, targeting BMP signaling in diabetes is proposed as a potential therapeutic strategy to halt the development of microvascular dysfunction in retinal diseases, particularly in DR. The goal of this review article is to discuss the biological functions of BMPs, their underlying mechanisms and their potential role in the pathogenesis of DR in particular.
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页数:12
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