p62/SQSTM1 coding plasmid prevents age related macular degeneration in a rat model

被引:26
作者
Kolosova, Nataliya G. [1 ]
Kozhevnikova, Oyuna S. [1 ]
Telegina, Darya V. [1 ]
Fursova, Anzhela Zh [1 ,2 ]
Stefanova, Natalia A. [1 ]
Muraleva, Natalia A. [1 ]
Venanzi, Franco [4 ]
Sherman, Michael Y. [5 ]
Kolesnikov, Sergey I. [7 ,8 ,9 ]
Sufianov, Albert A. [6 ,11 ]
Gabai, Vladimir L. [3 ,10 ]
Shneider, Alexander M. [3 ,5 ,6 ]
机构
[1] RAS, Inst Cytol & Genet, SB, Novosibirsk, Russia
[2] Novosibirsk State Reg Clin Hosp, Novosibirsk, Russia
[3] CureLab Oncol Inc, Deadham, MA 02492 USA
[4] Univ Camerino, Sch Biosci, Camerino, Italy
[5] Ariel Univ, Dept Mol Biol, Ariel, Israel
[6] Sechenov First Moscow State Med Univ, Moscow, Russia
[7] Russian Acad Sci, Moscow, Russia
[8] Lomonosov Moscow State Univ, Moscow, Russia
[9] Res Ctr Family Hlth & Reprod Problems, Irkutsk, Russia
[10] Boston Univ, Sch Med, Dept Biochem, Boston, MA 02118 USA
[11] Fed Ctr Neurosurg, Tyumen, Russia
来源
AGING-US | 2018年 / 10卷 / 08期
基金
俄罗斯科学基金会;
关键词
p62/SQSTM1; age-related macular degeneration; inflammation; gliosis; OXYS rats; aging; retina; AMD-LIKE RETINOPATHY; ACCELERATED OXYS RATS; RETINAL-PIGMENT EPITHELIUM; CELL-DEATH; P62; PATHWAY; MITOCHONDRIA; INFLAMMATION; MACROPHAGES; EXPRESSION;
D O I
10.18632/aging.101537
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
P62/SQSTM1, a multi-domain protein that regulates inflammation, apoptosis, and autophagy, has been linked to age-related pathologies. For example, previously we demonstrated that administration of p62/SQSTM1-encoding plasmid reduced chronic inflammation and alleviated osteoporosis and metabolic syndrome in animal models. Herein, we built upon these findings to investigate effect of the p62-encoding plasmid on an age-related macular degeneration (AMD), a progressive neurodegenerative ocular disease, using spontaneous retinopathy in senescence-accelerated OXYS rats, as a model. Overall, the p62DNA decreased the incidence and severity of retinopathy. In retinal pigment epithelium (RPE), p62DNA administration slowed down development of the destructive alterations of RPE cells, including loss of regular hexagonal shape, hypertrophy, and multinucleation. In neuroretina, p62DNA prevented gliosis, retinal thinning, and significantly inhibited microglia/macrophages migration to the outer retina, prohibiting their subretinal accumulation. Taken together, our results suggest that the p62DNA has a strong retinoprotective effect in AMD.
引用
收藏
页码:2136 / 2147
页数:12
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