Role of Adiponectin Peptide I (APNp1) in Age-Related Macular Degeneration

被引:6
作者
Logan, Connor [1 ]
Lyzogubov, Valeriy [1 ]
Bora, Nalini [1 ]
Bora, Puran [1 ]
机构
[1] Univ Arkansas Med Sci, Pat & Willard Walker Eye Res Ctr, Jones Eye Inst, Dept Ophthalmol, 4301 West Markham, Little Rock, AR 72205 USA
关键词
age related macular degeneration; adiponectin; adiponectin receptor; neovascularization; adeno-associated virus; topical administration; INDUCED CHOROIDAL NEOVASCULARIZATION; RECEPTOR; MOUSE MODEL; ADIPOR1; CELL; PROLIFERATION; EXPRESSION; TACHYPHYLAXIS; BEVACIZUMAB; INHIBITION;
D O I
10.3390/biom12091232
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
Age-related macular degeneration (AMD) is an eye disease that can cause central vision loss, particularly in the elderly population. There are 2 classes of AMD, wet-type and dry-type. Wet-type involves excess angiogenesis around the macula, referred to as choroidal neovascularization (CNV). This can result in leaky vessels, often causing more severe vision loss than dry-type AMD. Adiponectin peptide 1 (APNp1) has been shown to slow the progression of CNV. Here, we used a mouse model and FITC-labeled APNp1 to determine if APNp1 could be delivered effectively as an eye drop. Our experiment revealed that topically applied FITC-APNp1 could reach the macula of the eye, which is crucial for treating wet-type AMD. We also tested delivery of APNp1 via injection of an adeno-associated virus (AAV) vector in a mouse model of CNV. AAV is a harmless virus easy to manipulate and is very often used for protein or peptide deliveries. Results revealed an increase in the expression of APNp1 in the retina and choroid over a 28-day period. Finally, we investigated the mechanism by which APNp1 affects CNV by examining the expression of adiponectin receptor 1 (AdipoR1) and proliferating cell nuclear antigen (PCNA) in the retinal and choroidal tissue of the mouse eyes. AdipoR1 and PCNA were overexpressed in these tissues in mice with laser-induced CNV compared to naive mice. Based on our data shown here, we think it will enhance our understanding of APNp1 as a therapeutic agent for wet-type AMD and possible treatment alternatives that could be more beneficial for patients.
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页数:10
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