Applications of Genome-Editing Technologies for Type 1 Diabetes.
Rana El NahasMohammad Ameen Al-AghbarLaura HerreroNicholas van PanhuysMeritxell Espino-GuarchPublished in: International journal of molecular sciences (2023)
Type 1 diabetes (T1D) is a chronic autoimmune disease characterized by the destruction of insulin-producing pancreatic β-cells by the immune system. Although conventional therapeutic modalities, such as insulin injection, remain a mainstay, recent years have witnessed the emergence of novel treatment approaches encompassing immunomodulatory therapies, such as stem cell and β-cell transplantation, along with revolutionary gene-editing techniques. Notably, recent research endeavors have enabled the reshaping of the T-cell repertoire, leading to the prevention of T1D development. Furthermore, CRISPR-Cas9 technology has demonstrated remarkable potential in targeting endogenous gene activation, ushering in a promising avenue for the precise guidance of mesenchymal stem cells (MSCs) toward differentiation into insulin-producing cells. This innovative approach holds substantial promise for the treatment of T1D. In this review, we focus on studies that have developed T1D models and treatments using gene-editing systems.
Keyphrases
- type diabetes
- crispr cas
- genome editing
- glycemic control
- mesenchymal stem cells
- induced apoptosis
- stem cells
- cell cycle arrest
- cardiovascular disease
- umbilical cord
- insulin resistance
- gene expression
- multiple sclerosis
- single cell
- endoplasmic reticulum stress
- metabolic syndrome
- bone marrow
- skeletal muscle
- genome wide
- drug delivery
- oxidative stress
- deep learning
- machine learning
- combination therapy
- risk assessment
- copy number
- cell proliferation