Unlocking Schizophrenia: Mitochondria Dysfunction at the Forefront

Summary: Researchers have identified a pivotal role of impaired mitochondrial function in the development of schizophrenia by examining the genetic risk factor 3q29 deletion syndrome.

The genetic condition, known to amplify schizophrenia risk by 40 times, displayed alterations in mitochondrial activity in both mice models and human brain organoids. This discovery aligns with findings from another genetic factor linked to schizophrenia, the 22q11 deletion syndrome.

The study paves the way for an enhanced understanding of schizophrenia’s neurobiology and opens potential avenues for effective therapeutic strategies.

Key Facts:

  1. 3q29 deletion syndrome elevates the risk of schizophrenia by about 40-fold and is prevalent in 1 in 30,000 individuals.
  2. Both 3q29 and 22q11 deletion syndromes indicate disrupted mitochondrial function as a critical factor in schizophrenia’s development.
  3. Despite assumptions in the scientific community, the findings suggest that chromosomal deletions linked to schizophrenia impact mitochondria’s function, essential for neuron connections, rather than directly altering proteins in synapses.

Source: Emory University

Researchers are gaining insights into how schizophrenia develops by studying the strongest known genetic risk factor. When a small portion of chromosome 3 is missing, called 3q29 deletion syndrome, it increases the risk for schizophrenia by about 40-fold.

By analyzing how patterns of altered gene activity overlap in two models of 3q29 deletion syndrome – in mice and in human brain organoids – scientists have spotted an unexpected change in brain cells: impaired mitochondrial function.

This shows mitochondria.
Finding that 3q29 cells have dysregulated mitochondria was also surprising because only one of the 22 genes in the deletion encodes a protein located in mitochondria. Credit: Neuroscience News

The findings converge with work on another genetic risk factor for schizophrenia, 22q11 deletion syndrome or DiGeorge syndrome, which has also been found to involve disrupted mitochondrial function.

The results are published in Science Advances.

“For genetic variants associated with schizophrenia, we want to understand the primary pathology at the cellular level,” says co-lead author Ryan Purcell, PhD, assistant professor of cell biology at Emory University School of Medicine. “This gives us a foothold, which may help cut through schizophrenia’s polygenic complexity and better understand the neurobiology.”

The research came out of a collaboration between researchers at Emory and Rutgers. At Emory, the collaboration included the laboratories of co-senior author Gary Bassell PhD, Steven Sloan PhD and Victor Faundez MD, PhD. The co-lead author is Emory postdoctoral fellow Esra Sefik PhD, now at Princeton.

Co-senior author Jennifer Mulle PhD, and colleagues first showed that 3q29 deletion was a risk factor for schizophrenia in 2010. Previously at Emory, Mulle is associate professor of psychiatry, neuroscience and cell biology at Rutgers.

“Our data give strong support to the hypothesis that mitochondrial dysregulation is a contributor to the development of schizophrenia,” Mulle says. “The interplay between mitochondrial dynamics and neuronal maturation is an important area for additional detailed and rigorous study. “

3q29 deletion syndrome has an estimated prevalence of about 1 in 30,000. In addition to increasing the risk for schizophrenia, 3q29 deletion can include intellectual disability, autism spectrum disorder and congenital heart defects.

The effect of 3q29 deletion on schizophrenia risk is more than any single known gene variant, but the contributions of individual genes within the deletion are still being unraveled.

The finding that various schizophrenia-associated chromosomal deletions converge on mitochondria runs counter to an expectation in the field that such mutations should alter proteins engaged in synapses: the connections between neurons.

However, mitochondria are critical for energy-hungry synapses’ function – so these models may not be in conflict. Further work is needed to know whether mitochondria at synapses are particularly vulnerable, Bassell says.

Finding that 3q29 cells have dysregulated mitochondria was also surprising because only one of the 22 genes in the deletion encodes a protein located in mitochondria. In contrast, the 22q11 deletion contains several genes encoding mitochondrial proteins. The 3q29 gene involved may instead regulate the production or importation of mitochondrial proteins, Purcell says.

Mitochondria are found in every cell — they consume oxygen to produce energy in the form of ATP (adenosine triphosphate). Mitochondria have their own genomes, but most of the proteins found inside them are encoded by genes in the cell’s nucleus.

As a result of altered mitochondrial function, 3q29 cells lack metabolic flexibility, meaning that they have difficulty adapting to changes in sources of energy. This may interfere with neuronal development, because maturing neurons need to switch to relying more on mitochondria for energy as they differentiate.

Supported by a recently awarded grant, Purcell is now assessing whether cells from people with 22q11 also display the same metabolic inflexibility.

“Eventually, we want to understand which cellular changes like these are linked to specific clinical outcomes, which could help in designing more effective therapeutic strategies,” Purcell says.

The results reported in Science Advances illustrate how 3q29 deletion affects the whole body, not just the brain; the effects on mitochondria are seen in kidney cells as well as in brain cells. Individuals with 3q29 deletion syndrome also tend to be smaller in size than typical, possibly because of altered fat metabolism.

Funding: The research was supported by the Brain & Behavior Research Foundation and the National Institute of Mental Health (F32MH124273, R56MH116994, R01MH110701, R01MH118534), along with the Georgia Clinical & Translational Science Alliance, an I3 (Imagine, Innovate and Innovate) grant from the Emory University School of Medicine and a gift from the Woodruff Fund.

About this schizophrenia and genetics research news

Author: Brian Katzowitz
Source: Emory University
Contact: Brian Katzowitz – Emory University
Image: The image is credited to Neuroscience News

Original Research: Open access.
Cross-species analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion” by Ryan Purcell et al. Science Advances


Cross-species analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion

The 1.6-megabase deletion at chromosome 3q29 (3q29Del) is the strongest identified genetic risk factor for schizophrenia, but the effects of this variant on neurodevelopment are not well understood.

We interrogated the developing neural transcriptome in two experimental model systems with complementary advantages: isogenic human cortical organoids and isocortex from the 3q29Del mouse model.

We profiled transcriptomes from isogenic cortical organoids that were aged for 2 and 12 months, as well as perinatal mouse isocortex, all at single-cell resolution. Systematic pathway analysis implicated dysregulation of mitochondrial function and energy metabolism.

These molecular signatures were supported by analysis of oxidative phosphorylation protein complex expression in mouse brain and assays of mitochondrial function in engineered cell lines, which revealed a lack of metabolic flexibility and a contribution of the 3q29 gene PAK2. 

Together, these data indicate that metabolic disruption is associated with 3q29Del and is conserved across species.

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