Study Explores What Tumor Cells and a Healthy Retina Have in Common

"We eat glucose and use it as a major energy source," said Du, an assistant professor in the School of Medicine's Department of Biochemistry and Department of Ophthalmology and Visual Sciences. Through a multistep chemical process, almost all of the healthy cells in our body fixate on turning this glucose into fuel that mitochondria--essentially, the cells' boiler rooms--can burn for energy. Less than 20 percent of the glucose is used to make raw materials for new cells.

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"But in tumor cells, it's almost the opposite," Du said. Tumor cells go out of their way to thwart the chemical reactions that would normally transform glucose into energy. Instead, they turn most of the glucose into cancer's basic components.

"It's like they're building different houses. When you're building houses, you need basic materials like wood and concrete. When cancers grow, they need membranes, lipids, nucleotides."

Du and his research team suspected that a specific protein, called mitochondrial pyruvate carrier 1, played a role in the retina's ability to scrap glucose for photoreceptor parts. MPC1 is crucial to getting a derivative of glucose--called pyruvate--into the cells' "boiler rooms," where it can be burned to power the cell. "But in almost all cancer cells, MPC1 is decreased because the cells do not want to move pyruvate into mitochondria," Du explained. The team removed all of the MPC1 from some of their animal models. In the rest of the models, they left intact. "It turns out, the small amount of glucose that is being used in the mitochondria is critical for mitochondrial function, photoreceptor function and viability," said Du.

The researchers observed that MPC1-deficient models had dramatically impaired vision. Compared to their counterparts with typical MPC1 expression, their photoreceptors functioned less than half as well, at all intensities of light.

The team also found that MPC1 depletion caused retinal degeneration. In addition, it damaged the structure of the retina's mitochondria in "very, very unique ways," Du said.

"One important factor in developing age-related macular degeneration is mitochondria not functioning very well. But people don't know exactly what causes it, and there is still no treatment," he said. Du's research may provide insight into how this poorly understood disease manifests in patients and how doctors can treat it. He and his colleagues are conducting experiments to determine whether fat can be used as an alternative fuel source for retinal mitochondria that can't use glucose properly.

Du also plans to study what happens when MPC1 is blocked on a cell-specific basis. "In this project, we blocked the whole retina. But in the next one, we want to block photoreceptors or glial cells to see how small molecules cross between them. We want to address cell-cell interactions." Such a project could have an impact beyond the diagnosis and treatment of eye diseases. It could even deepen neuroscientists' understanding of how brain cells interact.

Source: Eurekalert