Study finds nerve cells and blood vessels in eye ‘talk’ to prevent disease.
A new study from scientists at The Scripps Research Institute (TSRI) shows that nerve cells and blood vessels in the eye constantly talk to each other to maintain healthy blood flow and prevent disease. The new study found that these neurons produce a chemical critical for the survival of blood vessels and the survival and function of photoreceptors, the most important cells for maintaining sight.
The team state that the study has implications for treating diseases such as diabetic retinopathy and age-related macular degeneration, the leading causes of vision loss in adults. Since the eye is often a good model for understanding the workings of the brain, the findings also provide clues to major neurological diseases such as Alzheimer’s. The opensource study is published in The Journal of Clinical Investigation.
For such a small organ, the eye is extremely complex, explain the team. Light enters through the pupil and passes through four layers in the retina before reaching the light-sensitive photoreceptors. The retina has a very sophisticated architecture. Previous studies show that if there is a little extra fluid, some swelling or a few dead cells, light isn’t going to come through correctly and vision can be impaired. The second, intermediate layer of the retinal blood vessels seems to activate during periods of low oxygen and acts as a ‘reserve’ of blood vessels in the retina. When blood flow and oxygen levels are low, a transcription factor called hypoxia-inducible factor (HIF) triggers the production of a chemical called VEGF. The VEGF then prompts new blood vessel growth, bringing more oxygen to the area.
Unfortunately, these new blood vessels can leak blood and other fluids and obscure vision as shown in past studies. This is the case with age-related macular degeneration, a wet version of which causes vision loss in the center of the eye, and diabetic retinopathy, in which some people with diabetes develop blurry or patchy vision.
In the current study, the team focused on neurons called amacrine cells and horizontal cells, which have a known role in preprocessing, or adjusting, electrical signals transmitted to the brain from the photoreceptors after they have been stimulated by light photons. These cells first caught the researchers’ attention because they appear to wrap themselves around the blood vessels (all together called the vasculature) of the intermediate layer.
The team hypothesized these neurons were actually altering the way the vasculature forms and behaves. To try to find out, in one experiment the researchers knocked out the production of VEGF in the amacrine and horizontal cells in mice before they were born. They found that these mice never developed normal blood vessels in the intermediate layer, leading to degeneration of the photoreceptors and severe vision impairment. This was surprising since previous research had given no clues that these cells were an important source of VEGF.
The team set up further experiments to test whether amacrine and horizontal cells really did provide essential VEGF. Because HIF signals cells to produce VEGF, the researchers wondered whether deleting HIF in amacrine and horizontal cells would also stop the pipeline of VEGF and normal intermediate layer blood vessel development. Indeed, the researchers found that deleting the gene for one form of HIF, called Hif-1α, also led to a lack of blood vessels in this area and subsequent vision problems.
This provided further evidence that VEGF from the amacrine and horizontal cells really does make a difference in blood vessel growth. For an even better understanding of VEGF production in those cells, the researchers investigated the role of a protein called VHL (von Hippel-Lindau), which normally keeps HIF levels low. After knocking out the gene to produce VHL in amacrine and horizontal cells, the researchers observed high HIF levels in the current study, overproduction of VEGF and dangerous blood vessel overgrowth typical of many eye diseases. Finally, they used a technique called genetic ablation to kill the amacrine cells and horizontal cells altogether and found this resulted in a lack of normal vessel growth in the intermediate layer.
Together, the experiments confirmed that neurons and blood vessels in the intermediate layer communicate to keep blood vessels growing normally, striking a balance between providing enough blood and avoiding blood vessel overgrowth. In short the signals from these cells are fine-tuning this layer of the vasculature.
Since the retina is a direct extension of the brain and the only place in the body where the medical community can easily visualize neurons, blood vessels and other neurological players working together, the team state that the study not only has implications for treating vision loss, but also brain diseases such as Alzheimer’s, Parkinson’s and even amyotrophic lateral sclerosis (ALS).
The researchers state that patients with Alzheimer’s get protein deposits in the brain, with the data findings showing similar deposits in the backs of the eyes of patients who have macular degeneration. The team surmise that if they can better understand what leads to accumulations of these abnormal proteins in the eye, that will hopefully also give an insight into how this accumulation begins in the brain.
age-related macular degeneration, diabetic retinopathy, eye sight, genetic ablation, genetics, healthinnovations, manual body regulation, neuroinnovations, transcription factor, vision loss, whole-body manual regulation
Michelle Petersen View All
Michelle is a health industry veteran who taught and worked in the field before training as a science journalist.
Featured by numerous prestigious brands and publishers, she specializes in clinical trial innovation--expertise she gained while working in multiple positions within the private sector, the NHS, and Oxford University.
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