Scientists at the University of Manchester have uncovered how the internal mechanisms in nerve cells wire the brain. The  findings open up new avenues in the investigation of neurodegenerative  diseases by analysing the cellular processes underlying these  conditions.
Dr Andreas Prokop and his team at the Faculty of Life Sciences have been  studying the growth of axons, the thin cable-like extensions of nerve  cells that wire the brain. If axons don't develop properly this can lead  to birth disorders, mental and physical impairments and the gradual  decay of brain capacity during aging.
Axon growth is directed by the hand shaped growth cone which sits in the  tip of the axon. It is well documented how growth cones perceive  signals from the outside to follow pathways to specific targets, but  very little is known about the internal machinery that dictates their  behaviour.
Dr Prokop has been studying the key driver of growth cone movements, the  cytoskeleton. The cytoskeleton helps to maintain a cell's shape and is  made up of the protein filaments, actin and microtubules. Microtubules  are the key driving force of axon growth whilst actin helps to regulate  the direction the axon grows.
Dr Prokop and his team used fruit flies to analyse how actin and  microtubule proteins combine in the cytoskeleton to coordinate axon  growth. They focussed on the multifunctional proteins called  spectraplakins which are essential for axonal growth and have known  roles in neurodegeneration and wound healing of the skin.
What the team demonstrate in this recent paper is that spectraplakins  link microtubules to actin to help them extend in the direction the axon  is growing. If this link is missing then microtubule networks show  disorganised criss-crossed arrangements instead of parallel bundles and  axon growth is hampered.
By understanding the molecular detail of these interactions the team  made a second important finding. Spectraplakins collect not only at the  tip of microtubules but also along the shaft, which helps to stabilise  them and ensure they act as a stable structure within the axon.
This additional function of spectraplakins relates them to a class of  microtubule-binding proteins including Tau. Tau is an important player  in neurodegenerative diseases, such as Alzheimer's, which is still  little understood. In support of the author's findings, another  publication has just shown that the human spectraplakin, Dystonin,  causes neurodegeneration when affected in its linkage to microtubules.
Talking about his research Dr Prokop said: "Understanding cytoskeletal machinery at the cell level is a holy grail of current cell research that will have powerful clinical applications. Thus, cytoskeleton  is crucially involved in virtually all aspects of a cell's life,  including cell shape changes, cell division, cell movement, contacts and  signalling between cells, and dynamic transport events within cells.  Accordingly, the cytoskeleton lies at the root of many brain disorders. Therefore,  deciphering the principles of cytoskeletal machinery during the  fundamental process of axon growth will essentially help research into  the causes of a broad spectrum of diseases. Spectraplakins like at the heart of this machinery and our research opens up new avenues for its investigation"
What Dr Prokop's paper in the Journal of Neuroscience also demonstrates  is the successful research technique using the fruit fly Drosophila. The  team was able to replicate its findings regarding axon growth in mice  which in turn means the findings can be translated to humans.
Dr Prokop points out fruit flies provide ideal means to make sense of  these findings and essentially help to unravel the many mysteries of  neurodegeneration.
Dr Prokop continues: "Understanding how spectraplakins perform their  cellular functions has important implications for basic as well as  biomedical research. Thus, besides their roles during axon growth,  spectraplakins of mice and humans are clinically important for a number  of conditions and processes including skin blistering,  neuro-degeneration, wound healing, synapse formation and neuron  migration during brain development. Understanding spectraplakins in one  biological process will instruct research on the other clinically  relevant roles of these proteins."