Excessive degradation of our cells' power plants plays a vital role in the onset of mitochondrial disease in kids. These inherited metabolic disorders can have severe consequences like such as brain dysfunction and neurological impairment.
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Lack of Mitochondria can Cause Severe Disease in Kids"
‘Mitochondrial diseases are inherited metabolic disorders that affect around 1 in 4,300 people and are caused by dysfunctional mitochondria.
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Mitochondria are the power plants of our cells and are crucial for converting energy derived from our food into the energy currency that drives the cell's biochemical functions. Not surprisingly, organs that are mainly affected in patients are those with high energy demand, such as the brain, heart, skeletal muscles, eyes, and ears. In children, severe multisystem involvement and neurodegeneration are frequent manifestations.
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FBXL4 is a gene that is implicated in controlling mitochondrial function, and mutations in this gene are one of the most common causes of mitochondrial diseases. FBXL4 mutations have been linked to encephalopathy, a form of brain dysfunction, causing neurological impairment. The manifestations are impaired cognitive function, developmental regression, epileptic seizures, and other types of neurological deficits. Despite the severe consequences of FBXL4 mutations in humans, the function of the protein that FBXL4 codes for has remained poorly understood.
In the current study, researchers generated mice that lack FBXL4 and showed that these mice recapitulate important characteristics present in patients with FBXL4 mutations. They were able to demonstrate that the reduced mitochondrial function is caused by increased degradation of mitochondria via a process called autophagy.
In the absence of FBXL4, mitochondria are more frequently delivered to the lysosome, the recycling station of the cell that contains enzymes that break down organic compounds. FBXL4 thus acts as a break on mitochondrial degradation. Patients who lack FBXL4 have too few mitochondria in their tissues which leads to disease.
"Further studies are needed to explore the therapeutic potential of these findings, in particular, whether inhibition of the degradation of mitochondria may provide a new treatment strategy," says Nils-Göran Larsson.
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Source-Eurekalert