Detail of figS8_ERK_OPN



Project
Title
Time-lapse images of ERK activation in polymorphonuclear cells (PMN)
Description
NA
Release, Updated
2019-11-20
License
CC BY
Kind
Image data based on Experiment
File Formats
Data size
239.0 MB

Organism
M. musculus ( NCBITaxon:10090 )
Strain(s)
PMN expressing ERK biosensor and 4T1 tumor cells expressing Red fluorescent protein
Cell Line
-
Protein names
ERK

Datatype
Cell dynamics, ERK activation by FRET
Molecular Function (MF)
Biological Process (BP)
activation of MAPKK activity ( GO:0007555 )
Cellular Component (CC)
cell ( GO:0005623 )
Biological Imaging Method
XYZ Scale
XY: 0.764 micrometer/pixel, Z: 1 micrometer/slice
T scale
59.59 second for each time interval

Image Acquisition
Experiment type
FRET
Microscope type
MultiPhotonMicroscopy
Acquisition mode
-
Contrast method
Fluorescence
Microscope model
Olympus FV1200MPE-BX61WI
Detector model
-
Objective model
Olympus XLPLN 25XW-MP
Filter set

Summary of Methods
See details in Kamioka et al. (2017) Cancer Sci, 108(2): 226-235.
Related paper(s)

Yuji Kamioka, Kanako Takakura, Kenta Sumiyama, Michiyuki Matsuda (2017) Intravital Forster resonance energy transfer imaging reveals osteopontin-mediated polymorphonuclear leukocyte activation by tumor cell emboli., Cancer science, Volume 108, Number 2, pp. 226-235

Published in 2017 Feb

(Abstract) Myeloid-derived suppressor cells (MDSCs) cause paraneoplastic leukemoid reactions and facilitate tumor cell metastasis. However, the interaction of MDSCs with tumor cells in live tissue has not been adequately visualized. To accomplish this task, we developed an intravital imaging protocol to observe metastasized tumor cells in mouse lungs. For visualization of the activation of MDSCs, bone marrow cells derived from transgenic mice expressing a Forster resonance energy transfer biosensor for ERK were implanted into host mice. Under a two-photon excitation microscope, numerous polymorphonuclear cells (PMNs) were found to infiltrate the lungs of tumor-bearing mice in which 4T1 mammary tumor cells were implanted into the footpads. By Forster resonance energy transfer imaging, we found ERK activation in PMNs around the 4T1 tumor emboli in the lungs. Because antibody array analysis implied the involvement of osteopontin (OPN) in the metastasis of 4T1 cells, we further analyzed the effect of OPN knockdown. The OPN knockdown in 4T1 cells did not affect the cell growth, but markedly suppressed lung metastasis of 4T1 cells and ERK activation in PMNs in the lung. Intravenous injection of recombinant OPN restored the lung metastasis of OPN-deficient 4T1 cells, suggesting that OPN functioned in a paracrine manner. It has been reported that ERK activation of neutrophils causes NETosis and that PMNs promote metastasis of tumor cells by NETosis. In agreement with previous reports, the NETosis inhibitor DNase I inhibited lung metastasis of 4T1 cells. These observations suggest that OPN promotes metastasis of 4T1 cells by activating PMNs and inducing NETosis.
(MeSH Terms)

Contact
Yuji Kamioka , Kansai Medical University
Contributors
Yuji Kamioka, Kanako Takakura, Kenta Sumiyama, Michiyuki Matsuda

OMERO Dataset
OMERO Project
Source