Can CRISPR correct type 2 diabetes gene?


Swedish researchers have identified 395 genes that are differently expressed in people with type 2 diabetes. One of these (PAX5) has proven to be very strongly associated with impaired insulin secretion. Now, researchers want to investigate if it is possible to use the genetic CRISPR/Cas9 scissors to correct the gene’s activity.

The research team’s scientific paper was published in the Journal of Clinical Investigation (JCI) and showed that 395 genes are differently expressed in the pancreatic islets in individuals with type 2 diabetes. Of these, 94 of the genes were previously known. The study is based on analyses of insulin-producing cells from 283 individuals with or without type 2 diabetes. 

Karl Bacos, associate professor in experimental diabetes research at Lund University, who led the study along with professor Charlotte Ling, said: “One of the strengths of our new study is that we have been able to validate already known genes, at the same time as we have discovered many new genes that are differently expressed in individuals with type 2 diabetes. We have also been able to identify a gene that proved to be very strongly associated with impaired insulin secretion.”

Using CRISPR/Cas9 to correct type 2 diabetes gene PAX5

The gene in question is called PAX5. It has previously been shown to be associated with leukemia, but there are no known studies of the gene’s role in the pancreatic islets and diabetes. The researchers carried out several experiments in cultivated pancreatic insulin-producing cells from humans and rats where they studied how an altered expression of PAX5 affected insulin secretion. Their experiment showed that insulin secretion was impaired, and that cell death was increased when PAX5 was overexpressed. 

The researchers hope that this knowledge will be used in trials for developing new treatments of type 2 diabetes. Diabetes researcher and professor of epigenetics at Lund University, Charlotte Ling, heads a research group in diabetes and epigenetics at Lund University Diabetes Centre (LUDC). She wants to investigate if it is possible to use the CRISPR/Cas9 genetic scissors to correct the gene’s activity.

“Our long-term goal is to regulate the activity of PAX5 using the genetic scissors and that way restore PAX5 levels in individuals with type 2 diabetes,” said Ling.

Previous research at LUDC has shown there are patient groups who have difficulties with their insulin secretion. This subgroup has been called SIDD (severe insulin-deficient diabetes) and it is a group characterized by impaired insulin secretion. 

“It is possible that future treatments where we restore PAX5 levels can prove to be particularly beneficial to this group of patients. Type 2 diabetes is a growing global public health problem, and we urgently need to find new ways to treat the disease,” Ling said.

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