Detail of Fig5A_retruct_1



Project
Title
Time-lapse two-photon images of retruction of microglial processes having phagosome
Description
Time-lapse two-photon images of retruction of microglial processes having phagosome. Chennel1 is microglias, and channel2 is neurons.
Release, Updated
2024-12-14
License
CC BY
Kind
Image data
File Formats
.tif
Data size
6.7 GB

Organism
Mus musculus
Strain(s)
CX3CR1^{+/GFP}, Nes-CreER^{T2+/-}, Rosa-CAG-LSL- tdTomato^{+/-}
Cell Line
-

Datatype
-
Molecular Function (MF)
Biological Process (BP)
phagocytosis ( GO:0006909 )
Cellular Component (CC)
Biological Imaging Method
two-photon laser scanning microscopy ( Fbbi:00000254 )
time lapse microscopy ( Fbbi:00000249 )
X scale
0.499 micrometer/pixel
Y scale
0.499 micrometer/pixel
Z scale
1.5 micrometer/slice
T scale
267 second per time interval

Image Acquisition
Experiment type
-
Microscope type
-
Acquisition mode
-
Contrast method
-
Microscope model
-
Detector model
-
Objective model
-
Filter set
-

Summary of Methods
Kamei R, Okabe S. In vivo imaging of the phagocytic dynamics underlying efficient clearance of adult-born hippocampal granule cells by ramified microglia. Glia. 2023 Aug;71(8):2005-2023.
Related paper(s)

Ryosuke Kamei, Shigeo Okabe (2023) In vivo imaging of the phagocytic dynamics underlying efficient clearance of adult-born hippocampal granule cells by ramified microglia., Glia

Published in 2023 Apr 27 (Electronic publication in April 27, 2023, midnight )

(Abstract) The phagocytosis of dead cells by microglia is essential in brain development and homeostasis. However, the mechanism underlying the efficient removal of cell corpses by ramified microglia remains poorly understood. Here, we investigated the phagocytosis of dead cells by ramified microglia in the hippocampal dentate gyrus, where adult neurogenesis and homeostatic cell clearance occur. Two-color imaging of microglia and apoptotic newborn neurons revealed two important characteristics. Firstly, frequent environmental surveillance and rapid engulfment reduced the time required for dead cell clearance. The motile microglial processes frequently contacted and enwrapped apoptotic neurons at the protrusion tips and completely digested them within 3-6 h of the initial contact. Secondly, while a single microglial process engaged in phagocytosis, the remaining processes continued environmental surveillance and initiated the removal of other dead cells. The simultaneous removal of multiple dead cells increases the clearance capacity of a single microglial cell. These two characteristics of ramified microglia contributed to their phagocytic speed and capacity, respectively. Consistently, the cell clearance rate was estimated to be 8-20 dead cells/microglia/day, supporting the efficiency of removing apoptotic newborn neurons. We concluded that ramified microglia specialize in utilizing individual motile processes to detect stochastic cell death events and execute parallel phagocytoses.

Contact
Shigeo Okabe , University of Tokyo , Department of Cellular Neurobiology, Graduate School of Medicine , Department of Cellular Neurobiology, Graduate School of Medicine
Contributors
Ryosuke Kamei

OMERO Dataset
OMERO Project
Source