Enzyme pair play crucial role in maintaining balance of cellular processes

"Our results show that the involvement of ULK1 and ULK2 in ER-to-Golgi trafficking is essential for cellular homeostasis and protecting the well-being of the cell," said corresponding author Mondira Kundu, M.D., Ph.D., associate member of the St. Jude Department of Pathology. "Under typical physiological conditions, the role of ULK1 and ULK2 in trafficking of proteins is more important than its role in autophagy, at least in brain cells."

Autophagy maintains cellular homeostasis by recycling intermediate metabolites sequestered within double-membrane-bound vesicles, like phagosomes. The ER serves as a platform and a source of membranes for this process. Although the researchers were expecting autophagy to be defective when both enzymes were impaired, they were surprised stress arose in the ER that resulted in selective loss of neurons in the brains of mice (hippocampal neurons). Restoring ER-to-Golgi trafficking in cells deficient in the two enzymes quelled the ER stress response.

Mice engineered to lack the ULK 1 and 2 enzymes in the central nervous system showed a loss of neurons in the brain. Neuronal death was linked to the activation of the unfolded protein response, a cellular stress response that takes place in the ER. By looking at the proteins involved in this response the researchers were able to identify a key partner protein involved in the process. They also determined that phosphorylation of this protein was an important control point in the trafficking process that delivers proteins to the cell surface. The unexpected roles for ULK1 and ULK2 in promoting ER-to-Golgi trafficking of proteins, which seem to have been conserved throughout evolution, appear to be essential for maintaining cellular homeostasis and the integrity of the cell.