Findings may lead to improved insulin-secreting cells derived from stem …

Diabetes researchers at Washington University School of Medicine in St. Louis have uncovered at least one reason insulin-secreting cells made from stem cells in the lab dont work as well as natural cells. The discovery could help speed progress toward making insulin-secreting cells called islet beta cells more effective in the treatment of insulin-dependent Type 1 diabetes.

Since scientists first discovered they could sample skin cells or fat cells from people, convert those cells into stem cells and then guide the stem cells to develop into insulin-secreting beta cells, researchers have been attempting to hone the process. The researchers say the new findings, published May 15 in the journal Nature Cell Biology, may help pave the way for producing more efficient and effective beta cells to treat people with insulin-dependent diabetes.

We have learned several things that could have immediate therapeutic potential for people with diabetes, said senior investigatorJeffrey R. Millman, an associate professor of medicine and of biomedical engineering. Our findings demonstrate that current methods for generating stem cell-derived beta cells may not be as useful as we would like in treating diabetes.

In this study, the research team used sophisticated single-cell sequencing technology to learn why some beta cells made from stem cells turn out to be less mature and less efficient at making insulin than their natural counterparts.

Using a technique called single-cell multiomic sequencing, the researchers compared stem cell-derived beta cells to natural beta cells and found that cells made from stem cells often didnt make as much insulin in response to glucose. In addition, sometimes the cells genetic profiles were closer to other cell types found in the gut, such as liver cells or intestinal cells.

Using machine learning and computational methods to examine a vast dataset of DNA from individual beta cells, Millmans team learned that one reason stem cell-derived beta cells tend to be immature involves irregularities in a substance called chromatin in the cells. Chromatin helps open and close various genes in the beta cells. The researchers would prefer, for one, that the chromatin in the cells keep insulin-secreting genes more open and active while closing down genes that make cells behave more like liver cells, breaking down fat rather than secreting insulin.

Having learned about chromatin differences between natural beta cells and stem-cell derived beta cells, we believe it will be possible to regulate chromatin to improve the quality of stem-cell derived beta cells, as well as the quantity of the cells that we can produce, Millman said.

He explained that each year about 60,000 people in the United States are diagnosed with insulin-dependent Type 1 diabetes. Experts estimate that curing diabetes in that many people would require about 60 trillion functioning beta cells.

But if we can make the cells more efficient, perhaps we could cut that number in half, Millman said. Were a long way from being able to do that, but the more efficient the beta cells are, the closer we will be to ramping up the manufacturing necessary to produce treatments.

In another development, Millmans team implanted stem cell-derived beta cells into mice and found that after six months, many of the deficiencies they had identified in such cells were corrected just by placing the cells into a natural environment, as opposed to a culture dish in the lab, suggesting that problems related to chromatin in stem cell-derived beta cells are fixable.

Washington University has licensed Millmans intellectual property to Sana Biotechnology with the goal of making future stem cell-derived therapies for diabetes available to patients.

Diabetes is a devastating, chronic illness, Millman said. For many years, our goal has been to help people with diabetes make their own insulin in response to glucose. These findings bring us one step closer to that goal.

Augsornworawat P, Hogrebe NJ, Ishahak M, Schmidt MD, Marquez E, Maestas MM, Veronese-Paniagua DA, Gale SE, Miller JR, Velazco-Cruz L, Millman JR. Single-nucleus multi-omics of human stem cell-derived islets identifies deficiencies in lineage specification. Nature Cell Biology, May 15, 2023.

The study was funded with support from the National Institute of Diabetes and Digestive and Kidney Diseases, the National Institute of General Medical Sciences, the National Cancer Institute, the National Center for Research Resources and the National Center for Advancing Translational Sciences of the National Institutes of Health (NIH). Grant numbers: R01 DK114233, R01 DK127497, T32 DK007120, T32 GM139774, F31 DK125068, P30 DK020579, UL1 TR002345 and P30 CA91842. Additional support from the Juvenile Diabetes Research Foundation, a National Science Foundation Graduate Research Fellowship, a Rita Levi-Montalcini Postdoctoral Fellowship in Regenerative Medicine, Siteman Cancer Center, the McDonnell Genome Institute, Childrens Discovery Institute and The Foundation for Barnes-Jewish Hospital.

About Washington University School of Medicine

WashU Medicineis a global leader in academic medicine, including biomedical research, patient care and educational programs with 2,800 faculty. Its National Institutes of Health (NIH) research funding portfolio is the third largest among U.S. medical schools, has grown 52% in the last six years, and, together with institutional investment, WashU Medicine commits well over $1 billion annually to basic and clinical research innovation and training. Its faculty practice is consistently within the top five in the country, with more than 1,800 faculty physicians practicing at 65 locations and who are also the medical staffs ofBarnes-JewishandSt. Louis Childrenshospitals ofBJC HealthCare. WashU Medicine has a storied history in MD/PhD training, recently dedicated $100 million to scholarships and curriculum renewal for its medical students, and is home to top-notch training programs in every medical subspecialty as well as physical therapy, occupational therapy, and audiology and communications sciences.

Originally published by the School of Medicine

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