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  3. Collective ERK/Akt activity waves orchestrate epithelial homeostasis by driving apoptosis-induced survival.
 

Collective ERK/Akt activity waves orchestrate epithelial homeostasis by driving apoptosis-induced survival.

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BORIS DOI
10.48350/156706
Publisher DOI
10.1016/j.devcel.2021.05.007
PubMed ID
34081908
Description
Cell death events continuously challenge epithelial barrier function yet are crucial to eliminate old or critically damaged cells. How such apoptotic events are spatio-temporally organized to maintain epithelial homeostasis remains unclear. We observe waves of extracellular-signal-regulated kinase (ERK) and AKT serine/threonine kinase (Akt) activity pulses that originate from apoptotic cells and propagate radially to healthy surrounding cells. This requires epidermal growth factor receptor (EGFR) and matrix metalloproteinase (MMP) signaling. At the single-cell level, ERK/Akt waves act as spatial survival signals that locally protect cells in the vicinity of the epithelial injury from apoptosis for a period of 3-4 h. At the cell population level, ERK/Akt waves maintain epithelial homeostasis (EH) in response to mild or intense environmental insults. Disruption of this spatial signaling system results in the inability of a model epithelial tissue to ensure barrier function in response to environmental insults.
Date of Publication
2021-06-21
Publication Type
Article
Subject(s)
500 - Science::570 - Life sciences; biology
Keyword(s)
Akt EGFR ERK apoptosis epithelial homeostasis fluorescent biosensors optogenetics signaling dynamics single-cell biology
Language(s)
en
Contributor(s)
Gagliardi, Paolo Armando
Institut für Zellbiologie (IZB)
Dobrzyński, Maciej
Jacques, Marc-Antoine Frédéric Roméo
Institut für Zellbiologie (IZB)
Dessauges, Coralie
Institut für Zellbiologie (IZB)
Ender, Pascal Peter
Institut für Zellbiologie (IZB)
Blum, Yannick
Hughes, Robert M
Cohen, Andrew R
Pertz, Olivier
Institut für Zellbiologie (IZB)
Additional Credits
Institut für Zellbiologie (IZB)
Series
Developmental cell
Publisher
Elsevier
ISSN
1878-1551
Related URL(s)
https://doi.org/10.1101/2020.06.11.145573
Access(Rights)
open.access
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