A sensitive red/far-red photoswitch for controllable gene therapy in mouse models of metabolic diseases

Nat Commun. 2024 Nov 27;15(1):10310. doi: 10.1038/s41467-024-54781-2.

Abstract

Red light optogenetic systems are in high demand for the precise control of gene expression for gene- and cell-based therapies. Here, we report a red/far-red light-inducible photoswitch (REDLIP) system based on the chimeric photosensory protein FnBphP (Fn-REDLIP) or PnBphP (Pn-REDLIP) and their interaction partner LDB3, which enables efficient dynamic regulation of gene expression with a timescale of seconds without exogenous administration of a chromophore in mammals. We use the REDLIP system to establish the REDLIP-mediated CRISPR-dCas9 (REDLIPcas) system, enabling optogenetic activation of endogenous target genes in mammalian cells and mice. The REDLIP system is small enough to support packaging into adeno-associated viruses (AAVs), facilitating its therapeutic application. Demonstrating its capacity to treat metabolic diseases, we show that an AAV-delivered Fn-REDLIP system achieved optogenetic control of insulin expression to effectively lower blood glucose levels in type 1 diabetes model mice and control an anti-obesity therapeutic protein (thymic stromal lymphopoietin, TSLP) to reduce body weight in obesity model mice. REDLIP is a compact and sensitive optogenetic tool for reversible and non-invasive control that can facilitate basic biological and biomedical research.

MeSH terms

  • Animals
  • Blood Glucose / metabolism
  • CRISPR-Cas Systems
  • Cytokines / metabolism
  • Dependovirus* / genetics
  • Diabetes Mellitus, Type 1 / genetics
  • Diabetes Mellitus, Type 1 / metabolism
  • Diabetes Mellitus, Type 1 / therapy
  • Disease Models, Animal*
  • Gene Expression Regulation
  • Genetic Therapy* / methods
  • HEK293 Cells
  • Humans
  • Insulin / metabolism
  • Light
  • Male
  • Metabolic Diseases / genetics
  • Metabolic Diseases / therapy
  • Mice
  • Mice, Inbred C57BL
  • Obesity / genetics
  • Obesity / metabolism
  • Obesity / therapy
  • Optogenetics* / methods
  • Tumor Necrosis Factor Ligand Superfamily Member 14

Substances

  • Insulin
  • Cytokines
  • Blood Glucose
  • Tnfsf14 protein, mouse
  • Tumor Necrosis Factor Ligand Superfamily Member 14