In vivo Caspase tracker biosensor system for detecting anastasis and non-apoptotic caspase activity

Ho Lam Tang, Ho Man Tang, Ming Chiu Fung, J Marie Hardwick

Research output: Contribution to journalArticle

Abstract

The discovery that mammalian cells can survive late-stage apoptosis challenges the general assumption that active caspases are markers of impending death. However, tools have not been available to track healthy cells that have experienced caspase activity at any time in the past. Therefore, to determine if cells in whole animals can undergo reversal of apoptosis, known as anastasis, we developed a dual color CaspaseTracker system for Drosophila to identify cells with ongoing or past caspase activity. Transient exposure of healthy females to environmental stresses such as cold shock or starvation activated the CaspaseTracker coincident with caspase activity and apoptotic morphologies in multiple cell types of developing egg chambers. Importantly, when stressed flies were returned to normal conditions, morphologically healthy egg chambers and new progeny flies were labeled by the biosensor, suggesting functional recovery from apoptotic caspase activation. In striking contrast to developing egg chambers, which lack basal caspase biosensor activation under normal conditions, many adult tissues of normal healthy flies exhibit robust caspase biosensor activity in a portion of cells, including neurons. The widespread persistence of Caspase Tracker-positivity implies that healthy cells utilize active caspases for non-apoptotic physiological functions during and after normal development.

Original languageEnglish (US)
Article number9015
JournalScientific Reports
Volume5
DOIs
StatePublished - 2015

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Biosensing Techniques
Caspases
Diptera
Ovum
Apoptosis
Starvation
Drosophila
Shock
Color
Neurons

ASJC Scopus subject areas

  • General

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In vivo Caspase tracker biosensor system for detecting anastasis and non-apoptotic caspase activity. / Tang, Ho Lam; Tang, Ho Man; Fung, Ming Chiu; Hardwick, J Marie.

In: Scientific Reports, Vol. 5, 9015, 2015.

Research output: Contribution to journalArticle

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