Summary: Neuregulin 3, a protein elevated in the brains of those with schizophrenia, suppresses a protein complex required for efficient neural communication, researchers report.
Source: Case Western Reserve.
An international team of researchers led by a Case Western Reserve University School of Medicine scientist has uncovered a novel mechanism in which a protein–neuregulin 3–controls how key neurotransmitters are released in the brain during schizophrenia. The protein is elevated in people with schizophrenia and other severe mental illnesses, but the study is the first to investigate how it causes such severe mental illness.
In a study published in the current issue of Proceedings of the National Academy of Sciences, neuroscientists from around the globe used genetic, electrophysiological, biochemical, and molecular techniques to uncover the function of neuregulin 3. They discovered it suppresses a protein complex required for proper neuron communication. The research team included 15 neuroscientists from across Case Western Reserve University School of Medicine, Louis Stokes Cleveland Veterans Affairs Medical Center, Augusta University of Georgia, plus Nanchang University and Guangzhou Medical University of China.
Certain variations in the gene encoding neuregulin 3 are considered risk factors for schizophrenia. The new study helps explain why neuregulin 3 is central to the disease. “We have identified a novel function of a schizophrenia susceptibility gene, neuregulin 3, which provides insight into cellular mechanisms of this devastating disorder and could lead to new therapeutic targets,” said senior author Lin Mei, PhD. Mei is professor and chair of the department of neurosciences at Case Western Reserve University School of Medicine. By understanding how neuregulin 3 acts in the brain, researchers could conceivably design drugs to restore its function during schizophrenia.
Schizophrenia affects nearly 1 in 100 American adults and is poorly understood, says Mei. It is difficult to tease apart the many interrelated proteins and neurotransmitters behind the disease. Mei’s study outlines a previously unknown mechanism found in neurons affected by schizophrenia.
In the new study, researchers mutated the gene encoding neuregulin 3 in mice–but only in certain populations of neurons. When they mutated neuregulin 3 in neurons that help activate the brain–called pyramidal neurons–the genetically modified mice displayed behavior consistent with schizophrenia. They had healthy hearing and reflexes, but were unusually active. They had trouble remembering and navigating mazes. In social interactions, the mice shied away from strangers. The experiments not only supported a role for neuregulin 3 in schizophrenia, but also helped define types of neurons involved.
By studying brain samples from the mice, the researchers learned how neuregulin 3 works at the cellular level. They found it inhibits assembly of a complex of proteins at synapses, the place where adjacent nerve cells communicate. Neurons need the complex, called SNARE, to transmit certain neurotransmitters between each other. In particular, SNARE complex helps neurons transmit glutamate–the most common “excitatory” neurotransmitter in the brain. Glutamate helps activate neurons and is essential for learning. Glutamate imbalances can cause schizophrenic symptoms.
People with severe mental illnesses like schizophrenia, bipolar disorder, and major depression, tend to have higher levels of neuregulin 3. The researchers mimicked protein levels found in the brains of schizophrenics by elevating neuregulin 3 in cultured neurons, and found higher levels of neuregulin 3 suppresses glutamate release. Cells with high levels of neuregulin 3 couldn’t form SNARE complexes properly. Too much of the inhibitory protein prevented the complex from forming, and suppressed glutamate levels in the brain cells. The researchers concluded that neuregulin 3 is critical to proper glutamate transmission in the brain.
According to Mei, the findings are particularly intriguing because they show neuregulin 3 works differently than other proteins in its family. Neuregulin 1, for example, activates an entirely different set of proteins in other types of neurons. The mechanism Mei’s team discovered for neuregulin 3 is even distinct from other roles previously described for the protein.
Said Mei, “In cancer biology, neuregulin 3 stimulates another risk gene of schizophrenia called ErbB4. Yet, unexpectedly, we found that neuregulin 3 in the brain may not act by activating ErbB4. Rather, it regulates glutamate release, and this novel function does not require ErbB4.”
The findings suggest neuregulin 3 could serve as a new therapeutic target to help treat schizophrenia or other mental illnesses. Drugs that target neuregulin 3 could help restore glutamate levels in certain types of neurons–a novel approach to schizophrenia treatment. “Identifying a novel mechanism of action is a prerequisite to understanding a disorder, and to development of therapeutic interventions,” Mei said. “Of course, the road could be long to get there, but we are on our way.”
[cbtabs][cbtab title=”MLA”]Case Western Reserve “Novel Mechanism Behind Schizophrenia Uncovered.” NeuroscienceNews. NeuroscienceNews, 21 February 2018. <https://neurosciencenews.com/schizophrenia-mechanism-8540/>.[/cbtab][cbtab title=”APA”]Case Western Reserve (2018, February 21). Novel Mechanism Behind Schizophrenia Uncovered. NeuroscienceNews. Retrieved February 21, 2018 from https://neurosciencenews.com/schizophrenia-mechanism-8540/[/cbtab][cbtab title=”Chicago”]Case Western Reserve “Novel Mechanism Behind Schizophrenia Uncovered.” https://neurosciencenews.com/schizophrenia-mechanism-8540/ (accessed February 21, 2018).[/cbtab][/cbtabs]
Controlling of glutamate release by neuregulin3 via inhibiting the assembly of the SNARE complex
Neuregulin3 (NRG3) is a growth factor of the neuregulin (NRG) family and a risk gene of various severe mental illnesses including schizophrenia, bipolar disorders, and major depression. However, the physiological function of NRG3 remains poorly understood. Here we show that loss of Nrg3 in GFAP-Nrg3f/f mice increased glutamatergic transmission, but had no effect on GABAergic transmission. These phenotypes were observed in Nex-Nrg3f/f mice, where Nrg3 was specifically knocked out in pyramidal neurons, indicating that Nrg3 regulates glutamatergic transmission by a cell-autonomous mechanism. Consequently, in the absence of Nrg3 in pyramidal neurons, mutant mice displayed various behavioral deficits related to mental illnesses. We show that the Nrg3 mutation decreased paired-pulse facilitation, increased decay of NMDAR currents when treated with MK801, and increased minimal stimulation-elicited response, providing evidence that the Nrg3 mutation increases glutamate release probability. Notably, Nrg3 is a presynaptic protein that regulates the SNARE-complex assembly. Finally, increased Nrg3 levels, as observed in patients with severe mental illnesses, suppressed glutamatergic transmission. Together, these observations indicate that, unlike the prototype Nrg1, the effect of which is mediated by activating ErbB4 in interneurons, Nrg3 is critical in controlling glutamatergic transmission by regulating the SNARE complex at the presynaptic terminals, identifying a function of Nrg3 and revealing a pathophysiological mechanism for hypofunction of the glutamatergic pathway in Nrg3-related severe mental illnesses.