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The nerve growth factor signaling and its potential as therapeutic target for glaucoma

journal contribution
posted on 2024-11-01, 17:00 authored by haitao Wang, Rikang Wang, Thilini ThrimawithanaThilini Thrimawithana, Peter Little AMPeter Little AM, Jiangping Xu, Zhong Ping Feng, Wenhua Zheng
Neuroprotective therapies which focus on factors leading to retinal ganglion cells (RGCs) degeneration have been drawing more and more attention. The beneficial effects of nerve growth factor (NGF) on the glaucoma have been recently suggested, but its effects on eye tissue are complex and controversial in various studies. Recent clinical trials of systemically and topically administrated NGF demonstrate that NGF is effective in treating several ocular diseases, including glaucoma. NGF has two receptors named high affinity NGF tyrosine kinase receptor TrkA and low affinity receptor p75NTR. Both receptors exist in cells in retina like RGC (expressing TrkA) and glia cells (expressing p75NTR). NGF functions by binding to TrkA or p75NTR alone or both together. The binding of NGF to TrkA alone in RGC promotes RGC's survival and proliferation through activation of TrkA and several prosurvival pathways. In contrast, the binding of NGF to p75NTR leads to apoptosis although it also promotes survival in some cases. Binding of NGF to both TrkA and p75NTR at the same time leads to survival in which p75NTR functions as a TrkA helping receptor. This review discusses the current understanding of the NGF signaling in retina and the therapeutic implications in the treatment of glaucoma.

History

Related Materials

  1. 1.
    DOI - Is published in 10.1155/2014/759473
  2. 2.
    ISSN - Is published in 23146141

Journal

BioMed Research International

Volume

2014

Number

759473

Start page

1

End page

10

Total pages

10

Publisher

Hindawi Publishing Corporation

Place published

United States

Language

English

Copyright

© 2014 HaitaoWang et al.

Former Identifier

2006049445

Esploro creation date

2020-06-22

Fedora creation date

2015-01-21

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