Dynamics of epithelial tissue remodeling in Drosophila pupa
Description
Epithelial tissues undergo cell turnover both during development and for homeostatic maintenance. Removal of cells is coordinated with the increase in number of newly dividing cells to maintain barrier function of the tissue. In Drosophila metamorphosis, larval epidermal cells (LECs) are replaced by adult precursor cells called histoblasts. Removal of LECs must counterbalance the exponentially increasing adult histoblasts. Previous work showed that the LEC removal accelerates as endocytic activity decreases throughout all LECs. Here, we show that the acceleration is accompanied by a mode switching from isolated single-cell apoptosis to clustered ones induced by the endocytic activity reduction. The authors identify the epidermal growth factor receptor (EGFR) pathway via extracellular-signal regulated kinase (ERK) activity as the main components downstream of endocytic activity in LECs. The reduced ERK activity, caused by the decrease in endocytic activity, is responsible for the apoptotic mode switching. Initially, ERK is transiently activated in normal LECs surrounding a single apoptotic LEC in a ligand-dependent manner, preventing clustered cell death. Following the reduction of endocytic activity, LEC apoptosis events do not provoke these transient ERK up-regulations, resulting in the acceleration of the cell elimination rate by frequent clustered apoptosis. These findings contrasted with the common perspective that clustered apoptosis is disadvantageous. Instead, switching to clustered apoptosis is required to ccommodate the growth of neighboring tissues.
Release date
2026-10-01
Updated date
-
License
CC BY 4.0
Kind
Image data
based on Experiment
Number of Datasets
18
( Image datasets: 18,
Quantitative data datasets: 0 )
pupal development programmed cell death tissue morphogenesis
Cellular Component (CC)
nucleus cytosol, nucleus
Biological Imaging Method
confocal microscopy
T scale
10 minutes, 5 minutes
Image Acquisition
Experiment type
-
Microscope type
-
Acquisition mode
-
Contrast method
-
Microscope model
-
Detector model
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Objective model
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Filter set
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Related paper(s)
Contact
Erina Kuranaga, Daiki Umetsu
, Kyoto University, Osaka University
, Graduate School and Faculty of Pharmaceutical Sciences, Department of Biological Sciences, Graduate School of Science
, Graduate School and Faculty of Pharmaceutical Sciences, Department of Biological Sciences, Graduate School of Science