4.5 Article

Estrogen Protects Optic Nerve Head Astrocytes Against Oxidative Stress by Preventing Caspase-3 Activation, Tau Dephosphorylation at Ser422 and the Formation of Tau Protein Aggregates

期刊

CELLULAR AND MOLECULAR NEUROBIOLOGY
卷 41, 期 3, 页码 449-458

出版社

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s10571-020-00859-6

关键词

Brain; Central nervous system; Eye; Glaucoma; Neurofibrillary tangles; Phosphorylation; 17 beta-estradiol; Retina; Tau cleavage

资金

  1. National Institutes of Health
  2. National Eye Institute Grants [EY014227, EY022774]
  3. National Institute on Aging Grant [AG027956]
  4. National Center for Research Resources/National Institute of General Medical Sciences grant [RR027093]
  5. National Institutes of Health Clinical and Translational Science Award Grant [UL1 TR002366]
  6. Felix and Carmen Sabates Missouri Endowed Chair in Vision Research
  7. Research to Prevent Blindness

向作者/读者索取更多资源

Glaucoma is a neurodegenerative disorder that leads to vision loss due to damage to the optic nerve. Recent studies suggest that estrogen may help prevent neurodegenerative diseases like glaucoma by protecting nerve cells and reducing tau protein cleavage. This research indicates that maintaining estrogen levels could potentially reduce the sensitivity of the optic nerve to glaucomatous damage through controlling posttranslational modifications of tau protein.
Glaucoma is a neurodegenerative disorder that leads to the slow degeneration of retinal ganglion cells, and results in damage to the optic nerve and concomitant vision loss. As in other disorders affecting the viability of central nervous system neurons, neurons affected by glaucoma do not have the ability to regenerate after injury. Recent studies indicate a critical role for optic nerve head astrocytes (ONHAs) in this process of retinal ganglion cell degeneration. Cleavage of tau, a microtubule stabilizing protein and constituent of neurofibrillary tangles (NFT), plays a major part in the mechanisms that lead to toxicity in CNS neurons and astrocytes. Here, we tested the hypothesis that estrogen, a pleiotropic neuro- and cytoprotectant with high efficacy in the CNS, prevents tau cleavage, and hence, protects ONHAs against cell damage caused by oxidative stress. Our results indicate that estrogen prevents caspase-3 mediated tau cleavage, and thereby decreases the levels of the resulting form of proteolytically cleaved tau protein, which leads to a decrease in NFT formation, which requires proteolytically cleaved tau protein. Overall, our data propose that by stopping the reduction of estrogen levels involved with aging the sensitivity of the optic nerve to glaucomatous damage might be reduced. Furthermore, our data suggest that therapeutic use of estrogen may be beneficial in slowing or preventing the onset or severity of neurodegenerative diseases such as glaucoma and potentially also other degenerative diseases of the CNS through direct control of posttranslational modifications of tau protein.

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