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Neuroprotective Strategies for Retinal Ganglion Cell Degeneration: Current Status and Challenges Ahead
被引:85
作者:

Boia, Raquel
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Univ Coimbra, Fac Med, Coimbra Inst Clin & Biomed Res ICBR, P-3000548 Coimbra, Portugal
Univ Coimbra, Ctr Innovat Biomed & Biotechnol CIBB, P-3000548 Coimbra, Portugal Univ Coimbra, Fac Med, Coimbra Inst Clin & Biomed Res ICBR, P-3000548 Coimbra, Portugal

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Aires, Ines Dinis
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Univ Coimbra, Fac Med, Coimbra Inst Clin & Biomed Res ICBR, P-3000548 Coimbra, Portugal
Univ Coimbra, Ctr Innovat Biomed & Biotechnol CIBB, P-3000548 Coimbra, Portugal Univ Coimbra, Fac Med, Coimbra Inst Clin & Biomed Res ICBR, P-3000548 Coimbra, Portugal

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Ambrosio, Antonio Francisco
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Univ Coimbra, Fac Med, Coimbra Inst Clin & Biomed Res ICBR, P-3000548 Coimbra, Portugal
Univ Coimbra, Ctr Innovat Biomed & Biotechnol CIBB, P-3000548 Coimbra, Portugal
Assoc Innovat & Biomed Res Light & Image AIBILI, P-3000548 Coimbra, Portugal Univ Coimbra, Fac Med, Coimbra Inst Clin & Biomed Res ICBR, P-3000548 Coimbra, Portugal

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Santiago, Ana Raquel
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Univ Coimbra, Fac Med, Coimbra Inst Clin & Biomed Res ICBR, P-3000548 Coimbra, Portugal
Univ Coimbra, Ctr Innovat Biomed & Biotechnol CIBB, P-3000548 Coimbra, Portugal
Assoc Innovat & Biomed Res Light & Image AIBILI, P-3000548 Coimbra, Portugal Univ Coimbra, Fac Med, Coimbra Inst Clin & Biomed Res ICBR, P-3000548 Coimbra, Portugal
机构:
[1] Univ Coimbra, Fac Med, Coimbra Inst Clin & Biomed Res ICBR, P-3000548 Coimbra, Portugal
[2] Univ Coimbra, Ctr Innovat Biomed & Biotechnol CIBB, P-3000548 Coimbra, Portugal
[3] Univ Basque Country UPV EHU, Dept Cell Biol & Histol, Leioa 48940, Vizcaya, Spain
[4] Assoc Innovat & Biomed Res Light & Image AIBILI, P-3000548 Coimbra, Portugal
关键词:
retinal ganglion cells;
neurodegeneration;
axonal regeneration;
neuroprotection;
optic neuropathies;
NITRIC-OXIDE SYNTHASE;
NERVE GROWTH-FACTOR;
CILIARY NEUROTROPHIC FACTOR;
MYELIN-ASSOCIATED GLYCOPROTEIN;
MULLER GLIAL-CELLS;
PROMOTES AXONAL REGENERATION;
VISUAL-SYSTEM DEVELOPMENT;
A(3) ADENOSINE RECEPTOR;
NECROSIS-FACTOR-ALPHA;
FACTOR MESSENGER-RNA;
D O I:
10.3390/ijms21072262
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:
The retinal ganglion cells (RGCs) are the output cells of the retina into the brain. In mammals, these cells are not able to regenerate their axons after optic nerve injury, leaving the patients with optic neuropathies with permanent visual loss. An effective RGCs-directed therapy could provide a beneficial effect to prevent the progression of the disease. Axonal injury leads to the functional loss of RGCs and subsequently induces neuronal death, and axonal regeneration would be essential to restore the neuronal connectivity, and to reestablish the function of the visual system. The manipulation of several intrinsic and extrinsic factors has been proposed in order to stimulate axonal regeneration and functional repairing of axonal connections in the visual pathway. However, there is a missing point in the process since, until now, there is no therapeutic strategy directed to promote axonal regeneration of RGCs as a therapeutic approach for optic neuropathies.
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