Study sheds more light on early pancreatic cells' behaviour

Its activity and dynamics have remained a mystery, especially in the context of human development, because it is only active for a short period of time during pancreas development.

Scientists from the Max Planck Institute of Molecular Cell Biology and Genetics (MPI-CBG) in Dresden, Germany, and the Novo Nordisk Foundation at the University of Copenhagen, Denmark, used a novel technique to observe the gene's activity as well as the protein it produces in human pancreas cells to better understand the gene.

This will contribute to a better understanding of how thehormone-producing cellsof the pancreas develop and could pave the way to produce more of these cells for therapeutic purposes, such as the production and transplantation of these cells to patients suffering from diabetes.

The different cells in the pancreas control our blood sugar, such as beta cells that make insulin. Insulin helps lower our blood sugar. If these cells stop working or die, we can get sick with diabetes.

When our body is growing, all these special cells come from a single cell type in the pancreas, which is called a pancreatic endocrine progenitor. This cell uses a gene called NEUROG3 for a short time to do its job.

The research group of Anne Grapin-Botton, managing director at the MPI-CBG in Dresden, together with colleagues from the Novo Nordisk Foundation at the University of Copenhagen, set out to learn more about these special cells in the pancreas that use the gene NEUROG3 and to see how this gene behaves in single cells.

We used special tags to see NEUROG3 in these cells and watched how they move using a long-term live imaging method that generated videos, explains Belin Selcen Beydag-Tasz, the first author of the study, and continues: By looking at flat 2D and 3D models of human pancreas growth, we found out that the levels of the NEUROG3 gene were different in different cells. Some cells had a lot of this gene, and some had a little.

Surprisingly, despite this heterogeneity, all the cells that had detectable NEUROG3 formed cells producing hormones. Another surprising result was that NEUROG3 works about two times slower in humans than in mice, meaning it takes more time for the gene to do its job in humans compared to mice.

The researchers used the long-term live imaging method to see a process normally hidden in the mothers womb.

The brightness of the cells helped them combine the gene activity with how the cells were behaving. Using this method, the research team learned that another gene called KLK12 has a role in making cells move to start forming islets of Langerhans when the NEUROG3 gene starts working.

Anne Grapin-Botton, who supervised the study, summarizes, The cell culture systems we developed to understand how cells in human fetuses form organs are starting to bear fruit. In our study, we've learned a lot more about how certain gene activity during fetal development can lead to diabetes later in life. The results show that when producing endocrine cells for future therapeutic applications based on the transplantation of these cells into diabetic patients, there is some flexibility in the control of NEUROG3. (ANI)