Author
Listed:
- Akira Yokoi
(Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku
Nagoya University Institute for Advanced Research, Furo-cho, Chikusa-ku
Japan Science and Technology Agency (JST), FOREST, 4-1-8 Honcho, Kawaguchi)
- Kosuke Yoshida
(Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku
Nagoya University Institute for Advanced Research, Furo-cho, Chikusa-ku)
- Hirotaka Koga
(Japan Science and Technology Agency (JST), FOREST, 4-1-8 Honcho, Kawaguchi
Osaka University, 8-1 Mihogaoka, Ibaraki)
- Masami Kitagawa
(Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku
Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku)
- Yukari Nagao
(Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku)
- Mikiko Iida
(Nagoya University, Furo-cho, Chikusa-ku)
- Shota Kawaguchi
(Nagoya University, Furo-cho, Chikusa-ku)
- Min Zhang
(Nagoya University, Furo-cho, Chikusa-ku)
- Jun Nakayama
(National Cancer Center Research Institute, 5-1-1 Tsukiji, Chuo-ku
Osaka International Cancer Institute, 3-1-69 Otemae, Chuo-ku)
- Yusuke Yamamoto
(National Cancer Center Research Institute, 5-1-1 Tsukiji, Chuo-ku)
- Yoshinobu Baba
(Nagoya University, Furo-cho, Chikusa-ku
Nagoya University
National Institutes for Quantum Science and Technology (QST))
- Hiroaki Kajiyama
(Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku)
- Takao Yasui
(Nagoya University Institute for Advanced Research, Furo-cho, Chikusa-ku
Nagoya University, Furo-cho, Chikusa-ku
Nagoya University
Japan Science and Technology Agency (JST), PRESTO)
Abstract
Extracellular vesicles (EVs), including exosomes, are recognized as promising functional targets involved in disease mechanisms. However, the intravital heterogeneity of EVs remains unclear, and the general limitation for analyzing EVs is the need for a certain volume of biofluids. Here, we present cellulose nanofiber (CNF) sheets to resolve these issues. We show that CNF sheets capture and preserve EVs from ~10 μL of biofluid and enable the analysis of bioactive molecules inside EVs. By attaching CNF sheets to moistened organs, we collect EVs in trace amounts of ascites, which is sufficient to perform small RNA sequence analyses. In an ovarian cancer mouse model, we demonstrate that CNF sheets enable the detection of cancer-associated miRNAs from the very early phase when mice did not have apparent ascites, and that EVs from different locations have unique miRNA profiles. By performing CNF sheet analyses in patients, we identify further location-based differences in EV miRNA profiles, with profiles reflecting disease conditions. We conduct spatial exosome analyses using CNF sheets to reveal that ascites EVs from cancer patients exhibit location-dependent heterogeneity. This technique could provide insights into EV biology and suggests a clinical strategy contributing to cancer diagnosis, staging evaluation, and therapy planning.
Suggested Citation
Akira Yokoi & Kosuke Yoshida & Hirotaka Koga & Masami Kitagawa & Yukari Nagao & Mikiko Iida & Shota Kawaguchi & Min Zhang & Jun Nakayama & Yusuke Yamamoto & Yoshinobu Baba & Hiroaki Kajiyama & Takao Y, 2023.
"Spatial exosome analysis using cellulose nanofiber sheets reveals the location heterogeneity of extracellular vesicles,"
Nature Communications, Nature, vol. 14(1), pages 1-15, December.
Handle:
RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-42593-9
DOI: 10.1038/s41467-023-42593-9
Download full text from publisher
Most related items
These are the items that most often cite the same works as this one and are cited by the same works as this one.
- Z. L. Liu & X. Y. Meng & R. J. Bao & M. Y. Shen & J. J. Sun & W. D. Chen & F. Liu & Y. He, 2024.
"Single cell deciphering of progression trajectories of the tumor ecosystem in head and neck cancer,"
Nature Communications, Nature, vol. 15(1), pages 1-18, December.
- Zixiang Wang & Shourong Wang & Junchao Qin & Xiyu Zhang & Gang Lu & Hongbin Liu & Haiyang Guo & Ligang Wu & Victoria O. Shender & Changshun Shao & Beihua Kong & Zhaojian Liu, 2022.
"Splicing factor BUD31 promotes ovarian cancer progression through sustaining the expression of anti-apoptotic BCL2L12,"
Nature Communications, Nature, vol. 13(1), pages 1-18, December.
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-42593-9. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.