High TG2 levels translated to atrophy of neurons, depression-like symptoms and reduced levels of TrkB, the receptor for brain derived neurotrophic factor.
Elevated levels of transglutaminase 2, or TG2, were found in the brains of mice experiencing chronic stress - an animal model of depression - as well as the prefrontal cortex of depressed people who committed suicide. High TG2 levels in //the mouse translated to atrophy of neurons, depression-like symptoms and reduced levels of TrkB, the receptor for brain derived neurotrophic factor (BDNF), a brain-nourishing molecule that also aids connectivity, said Dr. Anilkumar Pillai, neuroscientist in the Department of Psychiatry and Health Behavior at the Medical College of Georgia at Augusta University.
‘In depression elevated TG2 makes less serotonin available, leaving insufficient levels to enable proper communication between neurons.’
When scientists overexpressed TrkB, it relieved the depression-like symptoms in their animal model. "If you don't have enough BDNF, then all the serotonin in the world won't help," said Pillai, corresponding author of the study in the Nature journal Molecular Psychiatry. Likewise, when they directly reduced TG2 levels using a drug or a viral vector, more BDNF signaling occurred and depressive symptoms abated, said Pillai, who suspects that the protein may be a powerful new target in the fight against depression.
They found TG2 levels increased in their animal model following administration of stress hormones and after several weeks of actual stress that mimics the lives of chronically stressed individuals. Both produced classic depressive behavior and increased TG2 levels in the prefrontal cortex, a region involved in complex thoughts, decision-making as well as mood and personality expression.
Serotonin is a major neurotransmitter in the brain involved in many functions, including mood regulation. Serotonin levels in a depressed patient's blood should be high because serotonin signaling in the brain is low, Pillai said. Blood levels can be used to help diagnose the condition that affects about 350 million people worldwide and is the leading cause of disability, according to the World Health Organization. Many cell types make serotonin. Interestingly, the vast majority of serotonin is made in the gut, but neurons do make some of their own, Pillai said.
Astrocytes make BDNF, whose levels are also low in depression. Although just how the two work together is an unfolding mystery. In this study, Pillai and his team further linked them by showing that treatment that increases serotonin availability - as most antidepressants do - also increased levels of the BDNF receptor through the action of RAC1. TG2 converts serotonin to RAC1, a protein that helps rejuvenate the BDNF receptor, TrkB.
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"Increased amounts of TG2 will eventually lead to decreased levels of RAC1, and BDNF signaling is just not happening," Pillai said.
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Source-Eurekalert