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Nerve cell discovery may lead to better treatment of nervous system diseases

Summary: The findings could have implications for new avenues of research for a range of neurodegenerative diseases, including ALS and Alzheimer’s disease.

Source: University of Bath

A discovery that could improve treatment options for patients with neurodegenerative diseases has been made by scientists from King’s College London and the University of Bath in the UK.

This discovery centers on a molecule that plays an important role in nerve cell development and is known to contribute to disease when it malfunctions.

Previously, this molecule was thought to be restricted to the nucleus of the cell (the organelle containing a cell’s DNA and separated from the rest of the cell by a membrane) but this new study confirms an earlier finding by the same team according to which it can also be found in the cytoplasm (the watery interior of a cell).

The study also demonstrates for the first time that the cytoplasmic pool of this protein is functionally active.

This discovery has important implications for research on neurodegenerative diseases such as Alzheimer’s disease and motor neuron disease.

The discovery, described in Current biology was carried out by Professor Corinne Houart of King’s College London in collaboration with Dr Nikolas Nikolaou of the Department of Life Sciences in Bath.

Loss of nerve function

Scientists have known for some time that splicing proteins – the molecules studied in this research – can sometimes aggregate and form insoluble complexes in the cytoplasm of the cell, and that these complexes can interfere with the function of a neuron (nerve cell), eventually causing the neuron to lose function and degenerate.

However, this study is the first to show that a major splicing protein can be found in protein/messenger RNA complexes (called RNA granules) in the axons of nerve cells.

Axons are the long projections that carry electrical impulses away from the body of the nerve cell, connecting neurons to neighboring neurons or transmitting information from neurons to body tissues (eg, muscle or skin).

Axon dysfunction is known to be the cause of many progressive neurological disorders, so the discovery of splicing proteins in this part of the nerve cell provides insight into the mechanism that could give rise to the disease.

Shaping the messenger RNA molecule

The researchers found that the splicing protein SNRNP70 binds to strands of messenger RNA (mRNA) and then shapes them. These strands carry the genetic information of DNA from the nucleus of a cell to the cytoplasm of the cell.

The information carried by mRNA is used to create other proteins, the building blocks of life. The team also found that the splicing protein is necessary for mRNA to move from the nerve cell body along axons to more peripheral parts of a neuron.

See also

This shows motor neurons
A zebrafish trunk segment. Motor neurons (green) send axons that innervate muscle fibers (red). 1 credit

Commenting on this research, which uses zebrafish as a genetic model system, Dr Nikolaou said: “When we interfered with the function of the splice protein, we found that motor neurons were not forming well. They failed to make connections where they should have, and they lost other important connections. This type of behavior is also seen in human neurodegeneration.

“However, when SNRNP70 was reintroduced only into the cytoplasm and axons of these neurons, it was sufficient to restore motor connectivity and neuronal function again”

Although a small freshwater fish, the zebrafish is a species with a nervous system remarkably similar to that found in humans.

In the next phase of this research, Dr. Nikolaou plans to explore the precise function of this protein in axons. “We know that proteins interact with other proteins, so what proteins does this molecule interact with? And what happens when we remove these complexes from the cytoplasm – how does this affect neuronal function? »

He added: “Now that we know that these types of molecules have a function outside the nucleus, we will have to approach neurodegeneration from a different angle, asking ourselves how these pathogenic aggregates interfere with the function of these proteins not only in the nucleus but also in the cytoplasm, and what role they play in the degradation of neurons. This is something that has not been thought of before.”

About this neuroscience research news

Author: Chris Melvin
Source: University of Bath
Contact: Chris Melvin – University of Bath
Image: Image is credited to Nikolas Nikolaou

Original research: The findings will appear in Current biology

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