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Электронный каталог: Chistyakov, D. V. - A Role of Pigment Epithelium-Derived Factor in Zinc-Mediated Mechanism of Neurodegeneration in Gl...
Chistyakov, D. V. - A Role of Pigment Epithelium-Derived Factor in Zinc-Mediated Mechanism of Neurodegeneration in Gl...

Статья
Автор: Chistyakov, D. V.
Communications Biology: A Role of Pigment Epithelium-Derived Factor in Zinc-Mediated Mechanism of Neurodegeneration in Gl...
б.г.
ISBN отсутствует
Автор: Chistyakov, D. V.
Communications Biology: A Role of Pigment Epithelium-Derived Factor in Zinc-Mediated Mechanism of Neurodegeneration in Gl...
б.г.
ISBN отсутствует
Статья
Chistyakov, D.V.
A Role of Pigment Epithelium-Derived Factor in Zinc-Mediated Mechanism of Neurodegeneration in Glaucoma / D.V.Chistyakov, V.Borshchevskiy, [a.o.]. – Text : electronic // Communications Biology. – 2025. – Vol. 8. – P. 965. – URL: https://doi.org/10.1038/s42003-025-08370-8. – Bibliogr.: 161.
Glaucoma is a neurodegenerative condition involving optic nerve damage and retinal ganglion cells death. Animal studies suggested that the pathway linking these events can be mediated by mobile zinc secreted into the intraretinal space and exerting cytotoxic effects. Whether this mechanism is relevant for human glaucoma and what are the targets of extracellular zinc is unknown. We report that increased zinc content in the aqueous humor and retina is indeed a characteristic of glaucomatous neuropathy, and excess extracellular zinc may be recognized by the key retinal neurotrophic factor PEDF. Biophysical and X-ray crystallographic studies show that PEDF coordinates zinc ions in five types of intermolecular high-affinity sites, leading to a decrease in negative surface charge and reversible oligomerization of the protein, thereby masking the target recognition sites responsible for its neurotrophic and antiangiogenic activities and collagen binding. Notably, PEDF secretion is enhanced in both glaucoma and retinal cell models in response to zinc stress; however, zinc binding negatively affects axogenic, differentiative and prosurvival functions of PEDF by suppressing its ability to activate receptor PEDF-R/PNPLA2. We suggest that glaucomatous neurodegeneration is associated with direct inhibition of PEDF signaling by extracellular zinc, making their complex a promising target for neuroprotective therapy.
ОИЯИ = ОИЯИ (JINR)2025
Chistyakov, D.V.
A Role of Pigment Epithelium-Derived Factor in Zinc-Mediated Mechanism of Neurodegeneration in Glaucoma / D.V.Chistyakov, V.Borshchevskiy, [a.o.]. – Text : electronic // Communications Biology. – 2025. – Vol. 8. – P. 965. – URL: https://doi.org/10.1038/s42003-025-08370-8. – Bibliogr.: 161.
Glaucoma is a neurodegenerative condition involving optic nerve damage and retinal ganglion cells death. Animal studies suggested that the pathway linking these events can be mediated by mobile zinc secreted into the intraretinal space and exerting cytotoxic effects. Whether this mechanism is relevant for human glaucoma and what are the targets of extracellular zinc is unknown. We report that increased zinc content in the aqueous humor and retina is indeed a characteristic of glaucomatous neuropathy, and excess extracellular zinc may be recognized by the key retinal neurotrophic factor PEDF. Biophysical and X-ray crystallographic studies show that PEDF coordinates zinc ions in five types of intermolecular high-affinity sites, leading to a decrease in negative surface charge and reversible oligomerization of the protein, thereby masking the target recognition sites responsible for its neurotrophic and antiangiogenic activities and collagen binding. Notably, PEDF secretion is enhanced in both glaucoma and retinal cell models in response to zinc stress; however, zinc binding negatively affects axogenic, differentiative and prosurvival functions of PEDF by suppressing its ability to activate receptor PEDF-R/PNPLA2. We suggest that glaucomatous neurodegeneration is associated with direct inhibition of PEDF signaling by extracellular zinc, making their complex a promising target for neuroprotective therapy.
ОИЯИ = ОИЯИ (JINR)2025