| Ganglion cell | |
| Location: | Varies by type |
| Function: | Varies but often excitatory projection |
| Neurotransmitter: | Varies but often glutamate |
| Morphology: | Varies |
In neurophysiology, a ganglion cell is a cell found in a ganglion (a cluster of neurons in the peripheral nervous system). Examples of ganglion cells include:
During the late 1800s, early 1900s, Spanish Neuroscientist and Pathologist Santiago Ramón y Cajal proposed Neuron theory which basically introduced the idea that the Nervous system contained cells called the Neuron. The process he used was called Golgi staining of the vertebrae retina. Cajal was able to differentiate between different types of Ganglion cell based on dendritic morphology, cell body and dendritic tree size, and number of sub layers in which they arborize/stratification layers. Through this study, he discovered that the ganglion cell distribution amongst vertebrates were pretty similar minus the Rods and cones in the retinas.
In the 1940s, American Neurologist Stephen Polyak[3] produced description of the Golgi-impregnated Cells that helped further classify types of Ganglion Cells. This data helped scientists get a better understanding of the ganglion cells present in the retinas of Mammals and Primates
In 1974, Boycott and Wassle created a scheme for the classification of Ganglion Cells that was found to be in the cat retina. These cells, alpha, beta, delta and gamma are seen to be linked with the X,Y and W types of physiology. Boycott and Wassle confirmed the idea of Cajal's Ox and Dog retina idea by naming the alpha and beta.
In 1978, the idea of the alpha and beta ganglion cells could be divided into different subgroups, sublamina a and sublamina b. Sublamina a contains dendrite cells containing OFF-center receptive fields while the Sublamina b contains On-center receptive fields.[4]
Glaucoma is a collection of diseases that damages the nerve in the eye / retina. The damage in the nerve has the possibility to cause blindness. You may not know you have a Glaucoma without an in-depth eye exam normally using the dilation method. There is no cure for a Glaucoma, but it may be treated if found early. It is unknown the cause of a Glaucoma, but those who may be at risk include:
Hereditary optic neuroretinopathy
There are two different types of Hereditary Optic Neuroretinopathy, those including Leber's hereditary optic neuropathy and Autosomal Dominant Optic Atrophy. The Leber's Neuropathy is caused by a mutation in the Mitochondrial DNA (the DNA located inside the chromosome) This is only obtainable through the mother. Some individuals are carriers and experience no symptoms. Symptoms of individuals who are affected by Leber's Neuropathy include:
Autosomal Dominant Optic Atrophy is a mutated gene in the autosomes (not sex-linked genes in humans chromosome pairs 1-22). This trait is present in anyone with the mutation in the autosome. The individual only needs one mutated gene to be affected. Symptoms of this condition include:
These diseases can be examined by tests such as Eye exams, Image testing and a look through family history.[6]
Parkinson's Disease is a condition that originates in the Nervous System and affects parts controlled by the nervous system. This disease is progressive, meaning it progressively gets worse overtime. A slow loss of Retinal Ganglion Cells may be observed overtime. List of symptoms include:
Those who are at risk include genes (through family members), toxins from the environment, and the presence of Lewy bodies.[7] [8]