Abstract

Diabetes mellitus (DM) is a widespread metabolic disease with a progressive incidence of morbidity and mortality worldwide. Despite extensive research, treatment options for diabetic patients remains limited. Although significant challenges remain, induced pluripotent stem cells (iPSCs) have the capacity to differentiate into any cell type, including insulin-secreting pancreatic β cells, highlighting its potential as a treatment option for DM. Several iPSC lines have recently been derived from both diabetic and healthy donors. Using different reprogramming techniques, iPSCs were differentiated into insulin-secreting pancreatic βcells. Furthermore, diabetes patient-derived iPSCs (DiPSCs) are increasingly being used as a platform to perform cell-based drug screening in order to develop DiPSC-based cell therapies against DM. Toxicity and teratogenicity assays based on iPSC-derived cells can also provide additional information on safety before advancing drugs to clinical trials. In this review, we summarize recent advances in the development of techniques for differentiation of iPSCs or DiPSCs into insulin-secreting pancreatic β cells, their applications in drug screening, and their role in complementing and replacing animal testing in clinical use. Advances in iPSC technologies will provide new knowledge needed to develop patient-specific iPSC-based diabetic therapies.

Highlights

  • Diabetes mellitus (DM), commonly referred to as diabetes, is the most widespread metabolic disease worldwide [1]

  • type 2 diabetes mellitus (T2DM) was previously known as non-insulin-dependent DM (NIDDM) or adult-onset diabetes, which is an age-related metabolic disease resulting from insulin resistance of peripheral tissues and inadequate insulin-secreting pancreatic β cell function [5,6,7]

  • We reported the functional activity of induced pluripotent stem cells (iPSCs)-derived insulin-secreting pancreatic β cells, which were reprogrammed from pancreas-derived epithelial cells of non-obese diabetic (NOD) mice, a model of autoimmune type 1 diabetes mellitus (T1DM) [88]

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Summary

Introduction

Diabetes mellitus (DM), commonly referred to as diabetes, is the most widespread metabolic disease worldwide [1]. T2DM was previously known as non-insulin-dependent DM (NIDDM) or adult-onset diabetes, which is an age-related metabolic disease resulting from insulin resistance of peripheral tissues and inadequate insulin-secreting pancreatic β cell function [5,6,7]. The third form of diabetes, gestational diabetes, which occurs when pregnant women develop high blood glucose levels; it is usually resolved after giving birth. Compensation and restoration of insulin-secreting pancreatic β cell function is the most promising approach for DM This approach can control blood glucose levels and regenerate functional insulin-secreting pancreatic β cells from adult cells [10]. Development of this treatment has not significantly advanced owing to limited phenotypic characterization of pancreatic stem cells.

Generation of iPSCs
Differentiation of iPSCs into Insulin-Secreting Pancreatic β Cells
In Vivo Maturation of iPSC-Derived Pancreatic β Cells
Application of iPS Cell-Derived Pancreatic Cells in Diabetes Mellitus Therapy
Disease Modeling and Drug Discovery with iPSCs
Current Challenges and Future Perspectives
Findings
Conclusions
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