Summary of ssbd-repos-000332

SSBD:database
URL

Name
ssbd-repos-000332 (332-Miyabara-tumor)
URL
DOI
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Title
In vivo optical imaging of tumor stromal cells with hypoxia-inducible factor activity
Description
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Submited Date
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Release Date
2024-12-14
Updated Date
-
License
Funding information
-
File formats
Data size
19.0 MB

Organism
Mus musculus
Strain
C57BL/6J, B6N-Tyr^{cBrd}/BrdCrCrl
Cell Line
E0771
Genes
-
Proteins
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GO Molecular Function (MF)
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GO Biological Process (BP)
detection of hypoxia
GO Cellular Component (CC)
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Study Type
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Imaging Methods
luminescence detection

Method Summary
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Related paper(s)

Hitomi Miyabara, Ryuichiro Hirano, Shigeaki Watanabe, John Clyde Co Soriano, Hitomi Watanabe, Takahiro Kuchimaru, Nobuo Kitada, Tetsuya Kadonosono, Shojiro A Maki, Gen Kondoh, Shinae Kizaka-Kondoh (2023) In vivo optical imaging of tumor stromal cells with hypoxia-inducible factor activity., Cancer science

Published in 2023 Jul 22 (Electronic publication in July 22, 2023, midnight )

(Abstract) Tumors contain various stromal cells, such as immune cells, endothelial cells, and fibroblasts, which contribute to the development of a tumor-specific microenvironment characterized by hypoxia and inflammation, and are associated with malignant progression. In this study, we investigated the activity of intratumoral hypoxia-inducible factor (HIF), which functions as a master regulator of the cellular response to hypoxia and inflammation. We constructed the HIF activity-monitoring reporter gene hypoxia-response element-Venus-Akaluc (HVA) that expresses the green fluorescent protein Venus and modified firefly luciferase Akaluc in a HIF activity-dependent manner, and created transgenic mice harboring HVA transgene (HVA-Tg). In HVA-Tg, HIF-active cells can be visualized using AkaBLI, an ultra-sensitive in vivo bioluminescence imaging technology that produces an intense near-infrared light upon reaction of Akaluc with the D-luciferin analog AkaLumine-HCl. By orthotopic transplantation of E0771, a mouse triple negative breast cancer cell line without a reporter gene, into HVA-Tg, we succeeded in noninvasively monitoring bioluminescence signals from HIF-active stromal cells as early as 8 days after transplantation. The HIF-active stromal cells initially clustered locally and then spread throughout the tumors with growth. Immunohistochemistry and flow cytometry analyses revealed that CD11b(+) F4/80(+) macrophages were the predominant HIF-active stromal cells in E0771 tumors. These results indicate that HVA-Tg is a useful tool for spatiotemporal analysis of HIF-active tumor stromal cells, facilitating investigation of the roles of HIF-active tumor stromal cells in tumor growth and malignant progression.

Contact(s)
Shinae Kizaka-Kondoh
Organization(s)
Tokyo Institute of Technology , School of Life Science and Technology
Image Data Contributors
Quantitative Data Contributors

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