The latest role of nerve-specific splicing factor PTBP1 in the transdifferentiation of glial cells into neurons

Wiley Interdiscip Rev RNA. 2023 Mar;14(2):e1740. doi: 10.1002/wrna.1740. Epub 2022 May 16.

Abstract

Central nervous system injury diseases can cause the loss of many neurons, and it is difficult to regenerate. The field of regenerative medicine believes that supplementing the missing neurons may be an ideal method for nerve injury repair. Recent studies have found that down-regulation of polypyrimidine tract binding protein 1 (PTBP1) expression can make glial cells transdifferentiate into different types of neurons, which is expected to be an alternative therapy to restore neuronal function. This article summarized the research progress on the structure and biological function of the PTBP family, the mutual regulation of PTBP1 and PTBP2, their role in neurogenesis, and the latest research progress in targeting PTBP1 to mediate the transdifferentiation of glial cells into neurons, which may provide some new strategies and new ideas for the future treatment of central nervous system injury and neurodegenerative diseases. This article is categorized under: RNA Processing > Splicing Regulation/Alternative Splicing.

Keywords: alternative splicing; glial cells; neurons; polypyrimidine tract binding protein 1; transdifferentiation.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternative Splicing
  • Cell Transdifferentiation*
  • Heterogeneous-Nuclear Ribonucleoproteins / genetics
  • Heterogeneous-Nuclear Ribonucleoproteins / metabolism
  • Neuroglia / metabolism
  • Neurons / metabolism
  • Polypyrimidine Tract-Binding Protein* / chemistry
  • Polypyrimidine Tract-Binding Protein* / genetics
  • Polypyrimidine Tract-Binding Protein* / metabolism
  • RNA Splicing Factors / metabolism

Substances

  • RNA Splicing Factors
  • Polypyrimidine Tract-Binding Protein
  • Heterogeneous-Nuclear Ribonucleoproteins