Summary of ssbd-repos-000128

SSBD:database
URL

Name
ssbd-repos-000128 (128-Muta-IECsERKDyn)
URL
DOI
-

Title
Fluorescence images and BDML file for quantitative information about mouse intestinal epithelial cells (IECs) extracellular signal-regulated kinase (ERK) activity dynamics
Description
-
Submited Date
-
Release Date
2021-09-30
Updated Date
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License
Funding information
-
File formats
Data size
62.5 GB

Organism
Mus musculus
Strain
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Cell Line
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Genes
Egfl6, ErbB2, Flna, Lrig3, Noggin, Troy, Wnt-3a, Wnt3a
Proteins
E-cadherin, EGFR, ERK

GO Molecular Function (MF)
NA
GO Biological Process (BP)
ERBB2-EGFR signaling pathway, ERBB2 signaling pathway, activation of MAPERK kinase, epidermal growth factor signaling pathway
GO Cellular Component (CC)
NA
Study Type
Intestines/cytology, Intestines, Time-Lapse Imaging, Transgenic, Cell Culture Techniques, MAP Kinase Signaling System, Mice, Epithelial Cells/metabolism, Gene Expression Profiling, Neoplastic, Neoplastic/genetics, Fluorescence, Extracellular Signal-Regulated MAP Kinases/genetics, Organoids, Time-Lapse Imaging/methods, Animals, Epithelial Cells (D004847), MAP Kinase Signaling System/genetics, Organoids/metabolism, Microscopy, Organoids/cytology, Inbred C57BL, Multiphoton, Extracellular Signal-Regulated MAP Kinases/metabolism, Extracellular Signal-Regulated MAP Kinases, Kinetics, Cell Transformation
Imaging Methods
time lapse microscopy, fluorescence microscopy, FRET

Method Summary
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Related paper(s)

Yu Muta, Yoshihisa Fujita, Kenta Sumiyama, Atsuro Sakurai, M Mark Taketo, Tsutomu Chiba, Hiroshi Seno, Kazuhiro Aoki, Michiyuki Matsuda, Masamichi Imajo (2018) Composite regulation of ERK activity dynamics underlying tumour-specific traits in the intestine., Nature communications, Volume 9, Number 1, pp. 2174

Published in 2018 Jun 5 (Electronic publication in June 5, 2018, midnight )

(Abstract) Acting downstream of many growth factors, extracellular signal-regulated kinase (ERK) plays a pivotal role in regulating cell proliferation and tumorigenesis, where its spatiotemporal dynamics, as well as its strength, determine cellular responses. Here, we uncover the ERK activity dynamics in intestinal epithelial cells (IECs) and their association with tumour characteristics. Intravital imaging identifies two distinct modes of ERK activity, sustained and pulse-like activity, in IECs. The sustained and pulse-like activities depend on ErbB2 and EGFR, respectively. Notably, activation of Wnt signalling, the earliest event in intestinal tumorigenesis, augments EGFR signalling and increases the frequency of ERK activity pulses through controlling the expression of EGFR and its regulators, rendering IECs sensitive to EGFR inhibition. Furthermore, the increased pulse frequency is correlated with increased cell proliferation. Thus, ERK activity dynamics are defined by composite inputs from EGFR and ErbB2 signalling in IECs and their alterations might underlie tumour-specific sensitivity to pharmacological EGFR inhibition.
(MeSH Terms)

Contact(s)
Masamichi Imajo
Organization(s)
Kyoto University , Graduate School of Biostudies , Laboratory of Bioimaging and Cell Signaling
Image Data Contributors
Quantitative Data Contributors

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