A protein controlling complex neuronal branching identified!

A protein controlling complex neuronal branching identified!

A protein called "MetastasisMetastasis-suppressor 1" (MTSS1) activates one pathway and inhibits another competing pathway, thus playing a dual role that determines how neuron branches in the brain form, according to research published in the journal Cell Reports.

Researchers wanted to investigate the role of MTSS1 in neuron branch development in Purkinje cells. These neurons are among the largest in the human brain, occupying the outer layer of the cerebellum, which is located at the brain's base. Purkinje cells are comprised of a large cell body and an intricate tree-shaped portion of branches. These branches grow to completely fill available space in order to uniformly receive information from the surrounding environment. But they also retract if they come into contact with other branches. This process allows the neurons to control branch growth to be able to cover the maximum area possible while minimizing inefficient redundancies.

Previous studies have shown that MTSS1 may be involved in Purkinje branch development, but the details of how it is involved were lacking.

The team found that inhibiting MTSS1 expression in Purkinje cells in baby mice led to incomplete growth of Purkinje branches, indicating MTSS1 is an important regulator of branch development. Computer simulations showed similar results.

Upon further investigation, they found that MTSS1 regulates actin, the protein that forms a skeletal basis of neuron branches, by two competing pathways. They showed that in Purkinje cells, MTSS1 activates a pathway called ARP2/3, which initiates growth of new actin filaments at a 70° angle from the 'mother filament'. MTSS1 also binds to and inhibits a protein, called DAAM1, which forms straight unbranched actin filaments, and thought to compete with ARP2/3.

Inhibiting MTSS1 was found to stimulate the growth of dendrites until they contact neighboring ones, causing them to retract. Authors show that MTSS1’s C terminus binds to DAAM1 and paused DAAM1-mediated F-actin polymerization. This is the first time MTSS1 has been identified as a DAAM1 inhibitor in vertebrate neurons. Thus, MTSS1 plays a dual role as a formin inhibitor and ARP2/3 activator in dendritic filopodia, determining final neuronal morphology.