Genetically encoded cell-death indicators (GEDI) to detect an early irreversible commitment to neurodegeneration

Nat Commun. 2021 Sep 6;12(1):5284. doi: 10.1038/s41467-021-25549-9.

Abstract

Cell death is a critical process that occurs normally in health and disease. However, its study is limited due to available technologies that only detect very late stages in the process or specific death mechanisms. Here, we report the development of a family of fluorescent biosensors called genetically encoded death indicators (GEDIs). GEDIs specifically detect an intracellular Ca2+ level that cells achieve early in the cell death process and that marks a stage at which cells are irreversibly committed to die. The time-resolved nature of a GEDI delineates a binary demarcation of cell life and death in real time, reformulating the definition of cell death. We demonstrate that GEDIs acutely and accurately report death of rodent and human neurons in vitro, and show that GEDIs enable an automated imaging platform for single cell detection of neuronal death in vivo in zebrafish larvae. With a quantitative pseudo-ratiometric signal, GEDIs facilitate high-throughput analysis of cell death in time-lapse imaging analysis, providing the necessary resolution and scale to identify early factors leading to cell death in studies of neurodegeneration.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biosensing Techniques*
  • Calcium / metabolism
  • Cell Death / genetics*
  • Cerebral Cortex / cytology
  • Cerebral Cortex / metabolism
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Disease Models, Animal
  • Embryo, Nonmammalian
  • Fluorescent Dyes / chemistry
  • Gene Expression Regulation, Developmental*
  • Genes, Reporter
  • Glutamic Acid / pharmacology
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism
  • Humans
  • Larva / cytology
  • Larva / genetics
  • Larva / growth & development
  • Larva / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Neurodegenerative Diseases / genetics*
  • Neurodegenerative Diseases / metabolism
  • Neurodegenerative Diseases / pathology
  • Neurons / cytology
  • Neurons / drug effects
  • Neurons / metabolism*
  • Primary Cell Culture
  • Rats
  • Rats, Long-Evans
  • Single-Cell Analysis / methods
  • Superoxide Dismutase-1 / genetics
  • Superoxide Dismutase-1 / metabolism
  • Zebrafish / embryology
  • Zebrafish / genetics
  • Zebrafish / metabolism
  • alpha-Synuclein / genetics
  • alpha-Synuclein / metabolism

Substances

  • DNA-Binding Proteins
  • Fluorescent Dyes
  • SOD1 protein, human
  • TARDBP protein, human
  • alpha-Synuclein
  • enhanced green fluorescent protein
  • Green Fluorescent Proteins
  • Glutamic Acid
  • Superoxide Dismutase-1
  • Calcium