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Abstract

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 new fluorescent biosensor called genetically encoded death indicator (GEDI). GEDI specifically detects an intracellular Ca2+ level that cells achieve early in the cell death process and marks a stage at which cells are irreversibly committed to die. The time-resolved nature of GEDI delineates a binary demarcation of cell life and death in real time, reformulating the definition of cell death. We demonstrate that GEDI acutely and accurately reports death of rodent and human neurons in vitro, and show GEDI enables a novel automated imaging platform for single cell detection of neuronal death in vivo in zebrafish larvae. With a quantitative pseudo-ratiometric signal, GEDI facilitates 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.

Competing Interest Statement

The authors have declared no competing interest.

Details

1009240
Title
Genetically encoded cell-death indicators (GEDI) to detect an early irreversible commitment to neurodegeneration
Publication title
bioRxiv; Cold Spring Harbor
Publication year
2021
Publication date
Mar 13, 2021
Section
New Results
Publisher
Cold Spring Harbor Laboratory Press
Source
BioRxiv
Place of publication
Cold Spring Harbor
Country of publication
United States
University/institution
Cold Spring Harbor Laboratory Press
Publication subject
ISSN
2692-8205
Source type
Working Paper
Language of publication
English
Document type
Working Paper
Publication history
 
 
Milestone dates
2019-08-14 (Version 1)
ProQuest document ID
2272977154
Document URL
https://www.proquest.com/working-papers/genetically-encoded-cell-death-indicators-gedi/docview/2272977154/se-2?accountid=208611
Copyright
© 2021. This article is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (“the License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Last updated
2021-03-25
Database
2 databases
  • ProQuest One Academic
  • ProQuest One Academic