Enhancement of Conditional Reprogramming Technology for Production of Functional Human Beta Cells

Project Abstract Insufficient supply of donor pancreatic islets to meet the demand for transplants severely limits therapeutic options for Type diabetic T D patients in whom insulin therapy is insufficient to control their disease And while there has been much recent success with the directed differentiation of human embryonic stem cells hu ESCs and human induced pluripotent stem cells hu iPSCs into pancreatic beta cells the process is still quite imperfect and inefficient To this end we have shown that Conditional Reprogrammed CR cell culture technology can support the significant expansion of human islet derived cells to at least one million fold amount Just as importantly our preliminary data indicates that CR propagated human cells can readily develop mature differentiation markers and functional phenotype in vitro To develop this promising technology into a practical option for human cell replacement therapy we seek to enhance the proliferative capacity of CR grown human cells through the use of a focused screening approach that we have used with success with other CR responsive cell types The optimization of the post CR expansion differentiation step is also a component of our proposal using reproduced findings from other labs on how cell surface interactions can help drive human cell maturation and functionality The ultimate test of using CR technology to expand human cells will be to use these cells in an animal model of T D and to assess their ability to modulate the disease pathology a return to euglycemia and production of human C peptide in the transplant receiving mice will be the positive hallmark of success Successful completion of these specific research aims will position us to propose a Phase II SBIR application focused on the preclinical development of CR technology into GLP efficacy and safety testing and cGMP compliant cell manufacturing Project Narrative on Relevance to Public Health Insufficient supply of donor organs to meet the demand for transplants severely limits therapeutic options for Type diabetic T D patients in whom insulin therapy is insufficient to control their disease And while there has been much success with the directed differentiation of human embryonic stem cells hu ESCs and human induced pluripotent stem cells hu iPSCs into pancreatic beta cells recently the process is still quite imperfect and inefficient Propagenix Conditional Reprogramming technology provides a fresh and unique approach that has the potential to overcome many of the existing issues with the current technologies This technology platform currently has the capability of expanding human cells by greater than one million fold and with the success on the objectives of this grant application could deliver the ability to expand human cells by one billion fold and in a manufacturing compatible system This advance would clearly change the current equation of islet donors per recipient T D patient to one where hundreds to thousands of patients could be treated from a single donor sample that had been propagated using Propagenix technology