Tools and Biomarkers for the Study of Retinal Ganglion Cell Degeneration.
Ciriaco Corral-DomengePedro de la VillaAlicia MansillaFrancisco GermainPublished in: International journal of molecular sciences (2022)
The retina is part of the central nervous system, its analysis may provide an idea of the health and functionality, not only of the retina, but also of the entire central nervous system, as has been shown in Alzheimer's or Parkinson's diseases. Within the retina, the ganglion cells (RGC) are the neurons in charge of processing and sending light information to higher brain centers. Diverse insults and pathological states cause degeneration of RGC, leading to irreversible blindness or impaired vision. RGCs are the measurable endpoints in current research into experimental therapies and diagnosis in multiple ocular pathologies, like glaucoma. RGC subtype classifications are based on morphological, functional, genetical, and immunohistochemical aspects. Although great efforts are being made, there is still no classification accepted by consensus. Moreover, it has been observed that each RGC subtype has a different susceptibility to injury. Characterizing these subtypes together with cell death pathway identification will help to understand the degenerative process in the different injury and pathological models, and therefore prevent it. Here we review the known RGC subtypes, as well as the diagnostic techniques, probes, and biomarkers for programmed and unprogrammed cell death in RGC.
Keyphrases
- cell death
- optic nerve
- cell cycle arrest
- diabetic retinopathy
- public health
- healthcare
- machine learning
- deep learning
- mental health
- induced apoptosis
- spinal cord
- optical coherence tomography
- stem cells
- white matter
- health information
- cell therapy
- bone marrow
- cell proliferation
- resting state
- quality improvement
- neuropathic pain
- social media
- spinal cord injury
- living cells
- brain injury
- subarachnoid hemorrhage
- signaling pathway