The research group, led by associate professorMinglin Mafrom theDepartment of Biological and Environmental Engineeringin the College of Agriculture and Life Sciences, partnered with stem cell biologists at Washington University School of Medicine in St. Louis to identify how to protect these islets to let them do their job safely.
Cornell doctoral student Xi Wang is the first author of the group’s paper, “A Nanofibrous Encapsulation Device For Safe Delivery of Insulin-producing Cells to Treat Type 1 Diabetes,” published June 2 in Science Translational Medicine. Postdoctoral researcher Daniel T. Bowers also contributed to the report.
Type 1 diabetes – which afflicts roughly 1.6 million Americans, including nearly 200,000 children and adolescents – causes insulin-producing pancreatic cell clusters (islets) to be destroyed by the body’s own immune system. Past research has shown that islets can be grown from stem cells and implanted into the body, but they need to be able to secrete insulin in response to blood sugar while also being protected from the body’s immune and autoimmune responses.
Ma’s team implanted a device containing islets or human stem-cell derived, insulin-secreting cells into diabetic mice, reversing their diabetes. By doing so, they eliminated the need for drugs to suppress the immune system from attacking islets.
“The combined structural, mechanical and chemical properties of the device we used kept other cells in the mice from completely isolating the implant and, essentially, choking it off and making it ineffective,” Ma said.
“The implants floated freely inside the animals, and when we removed them after about six months, the insulin-secreting cells inside the implants were still functioning. And importantly, it is a very robust and safe device.”
Think of the device as a tiny, micro-porous cage, about the width of several strands of hair, that gets implanted into the abdomen. The mesh of the cage safely encloses the islets to secrete insulin in response to blood sugar levels and gives them a steady flow of nutrients and oxygen to keep them alive, but protects them from the immune cells that are too big to get through.
Several implants have been tried in recent years, with varying levels of success, including earlierdevices made by Ma’s research team in 2018 that employed a similar, but less sturdy design.For this study, Ma and his colleagues developed what they call a nanofiber-integrated cell encapsulation (NICE) device – a safer, more effective method. They filled the implants with either islets or insulin-secreting beta cells that had been manufactured from stem cells, then implanted the devices into the abdomens of mice with diabetes.
