optimized-protocol-for-generating-functional-pancreatic-insulin

Optimized Protocol for Generating Functional Pancreatic Insulin-secreting Cells from Human Pluripotent Stem Cells

Human pluripotent stem cells (hPSCs) can differentiate into any kind of cell, making them an excellent alternative source of human pancreatic ...

Cell Biology and Functional Genomics

The inheritance of variants that lead to coding changes in, or the mis-expression of, genes critical to pancreatic beta cell function can lead to alterations in insulin secretion and increase the risk of both type 1 and type 2 diabetes. Recently developed clustered regularly interspaced short palindromic repeats (CRISPR/Cas9) gene editing tools provide a powerful means of understanding the impact of identified variants on cell function, growth, and survival and might ultimately provide a means, most likely after the transplantation of genetically "corrected" cells, of treating the disease. Here, we review some of the disease-associated genes and variants whose roles have been probed up to now. Next, we survey recent exciting developments in CRISPR/Cas9 technology and their possible exploitation for β cell functional genomics. Finally, we will provide a perspective as to how CRISPR/Cas9 technology may find clinical application in patients with diabetes.

Ines Cherkaoui

Department of Metabolism,
Digestion and Reproduction,
Faculty of Medicine,
Department of Metabolism, Digestion and Reproduction, Faculty of Medicine

Cell Biology and Functional Genomics

Optimized Protocol for Generating Functional Pancreatic Insulin-secreting Cells from Human Pluripotent Stem Cells

Ines Cherkaoui

.css-o250i3{font-size:18px;font-family:Open Sans,sans-serif;line-height:21.6px;}Department of Metabolism,Digestion and Reproduction,Faculty of Medicine,Department of Metabolism, Digestion and Reproduction, Faculty of Medicine

Cell Biology and Functional Genomics

Optimized Protocol for Generating Functional Pancreatic Insulin-secreting Cells from Human Pluripotent Stem Cells

Department of Metabolism,
Digestion and Reproduction,
Faculty of Medicine,
Department of Metabolism, Digestion and Reproduction, Faculty of Medicine