The role of noncoding RNAs in beta cell biology and tissue engineering

Life Sci. 2024 Jul 1:348:122717. doi: 10.1016/j.lfs.2024.122717. Epub 2024 May 12.

Abstract

The loss or dysfunction of pancreatic β-cells, which are responsible for insulin secretion, constitutes the foundation of all forms of diabetes, a widely prevalent disease worldwide. The replacement of damaged β-cells with regenerated or transplanted cells derived from stem cells is a promising therapeutic strategy. However, inducing the differentiation of stem cells into fully functional glucose-responsive β-cells in vitro has proven to be challenging. Noncoding RNAs (ncRNAs) have emerged as critical regulatory factors governing the differentiation, identity, and function of β-cells. Furthermore, engineered hydrogel systems, biomaterials, and organ-like structures possess engineering characteristics that can provide a three-dimensional (3D) microenvironment that supports stem cell differentiation. This review summarizes the roles and contributions of ncRNAs in maintaining the differentiation, identity, and function of β-cells. And it focuses on regulating the levels of ncRNAs in stem cells to activate β-cell genetic programs for generating alternative β-cells and discusses how to manipulate ncRNA expression by combining hydrogel systems and other tissue engineering materials. Elucidating the patterns of ncRNA-mediated regulation in β-cell biology and utilizing this knowledge to control stem cell differentiation may offer promising therapeutic strategies for generating functional insulin-producing cells in diabetes cell replacement therapy and tissue engineering.

Keywords: Diabetes; Hydrogel; Noncoding RNAs; Stem cells; Tissue engineering; β-Cell.

Publication types

  • Review

MeSH terms

  • Animals
  • Cell Differentiation* / genetics
  • Diabetes Mellitus / genetics
  • Diabetes Mellitus / metabolism
  • Diabetes Mellitus / therapy
  • Humans
  • Hydrogels
  • Insulin-Secreting Cells* / metabolism
  • RNA, Untranslated* / genetics
  • Stem Cells / cytology
  • Stem Cells / metabolism
  • Tissue Engineering* / methods