Researchers at Karolinska Institutet in Sweden show how a molecule they have identified stimulates the formation of new insulin-producing cells in zebrafish and mammalian tissue through a newly described mechanism for regulating protein synthesis. The results are published in Nature Chemical Biology.
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“Our findings indicate a new potential target for treating diabetes, in that we demonstrate a possible way of stimulating the formation of new insulin-producing cells,” says the study’s last author Olov Andersson, senior researcher at the Department of Cell and Molecular Biology at Karolinska Institutet.
Both type 1 and type 2 diabetes are characterized by raised levels of blood sugar, the result of low levels of endogenous insulin, the hormone needed for glucose uptake from the blood, or a physiological inability to utilize the insulin secreted – or both.
Insulin injections and glucose-lowering drugs can control the disease but not cure it.
Regeneration of pancreatic β cells
“One alternative could be a treatment that regulates blood glucose by increasing the number of insulin-producing pancreatic β cells, so we’re researching the possible regeneration of these cells,” says the study’s first author Christos Karampelias, a former doctoral student at the Department of Cell and Molecular Biology at Karolinska Institutet.
The team from Karolinska Institutet has previously identified a small molecule able to stimulate the regeneration of insulin-producing β cells. This they did by analyzing a large number of substances in a zebrafish model.
In this present study, they examined the molecular mechanism of this stimulation.
By analyzing many molecular interactions in yeast cells, the researchers show that their molecule binds to a protein called MNK2. Subsequent studies of zebrafish and cell cultures indicate that the molecule operates by regulating the translation of mRNA and boosting the synthesis of proteins, without which the formation of new β cells cannot be increased. Zebrafish, given the molecule, also showed lower blood glucose levels than controls.
The study also shows that the molecule can induce the formation of new pancreatic β cells from pigs and stimulate the expression of insulin in human organoids (organ-like cell formations).
Studies of human tissue
“We’ll now be studying the effect of this and similar molecules in human tissue and analyzing the molecule’s target protein, MNK2, in tissue from healthy donors and donors with diabetes,” says Dr. Andersson.
The studied molecule was found through studies on zebrafish, providing a valuable model for testing many potential diabetes drug candidates. Since the fish embryo is transparent, its development is easy to monitor with a microscope. Zebrafish larvae also have only one cluster of β cells, a so-called islet of Langerhans, which facilitates studies of how new β cells are formed after the population has been decreased in a way that mimics the onset of type 1 diabetes.
Source: Karolinska Institutet