Extracellular vesicles from senescent hepatic stellate cells promote cell viability of hepatoma cells through increasing EGF secretion from differentiated THP?1 cells

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Extracellular vesicles from senescent hepatic stellate cells promote cell viability of hepatoma cells through increasing EGF secretion from differentiated THP?1 cells

Material type: 博士論文

Author: 宮副, 由梨

Publisher: Spandidos Publications

Publication date: 2020-09-02

Material Format: Digital

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Name of awarding university/degree: Nagasaki University (長崎大学),博士(医学)

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Note (General)：: Since the discovery of the senescence?associated secretory phenotype, the role of senescent hepatic stellate cells (HSCs) in hepatocellular carcinoma ...

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Material Type: 博士論文
Title: Extracellular vesicles from senescent hepatic stellate cells promote cell viability of hepatoma cells through increasing EGF secretion from differentiated THP?1 cells
Author/Editor: 宮副, 由梨
Author Heading: 宮副, 由梨
Publication, Distribution, etc.: Spandidos Publications
Publication Date: 2020-09-02
Publication Date (W3CDTF): 2020-09-02
Alternative Title: 老化肝星細胞から分泌される細胞外小胞は、分化THP-1細胞からのEGF発現増加を介し肝癌細胞増殖能を促進させる
Periodical title: Biomedical Reports
No. or year of volume/issue: 12 4
Volume: 12
Issue: 4
Pages: 163-170
ISSN (Periodical Title): ISSN : 2049-9434
ISSN : 2049-9442
Degree grantor/type: Nagasaki University (長崎大学)
Date Granted: 2020-09-02
Dissertation Number: 甲医歯薬第1274号
Degree Type: 博士(医学)
Text Language Code: eng
Subject Heading: epidermal growth factor
etoposide
extracellular vesicles
hepatic stellate cells
hepatocellular carcinoma
senescence?associated secretory phenotype
Target Audience: 一般
Note (General): Since the discovery of the senescence?associated secretory phenotype, the role of senescent hepatic stellate cells (HSCs) in hepatocellular carcinoma (HCC) development has gained increasing attention. Similar to cytokines, extracellular vesicles (EVs) are essential for intercellular communication. However, the function of EVs derived from senescent HSCs in HCC progression has not been extensively studied. The aims of the present study were to characterize the EVs derived from senescent HSCs and determine their role in the tumor microenvironment. Cellular senescence was induced in human hepatic stellate cells (HHSteCs) with various concentrations of etoposide. Induction was confirmed using EdU staining and 53BP1 and p21 immunostaining. EVs were isolated by ultracentrifugation and analyzed by nanoparticle tracking analysis. Multiplex immunoassays were used to compare the levels of growth factors secreted from hepatoma cell lines and macrophage cells pretreated with EVs derived from senescent HHSteCs (senescent EVs) with those pretreated with EVs derived from normal cultured HHSteCs (normal EVs). Treatment with 25 μM etoposide for 3 days was the most effective at inducing senescence in HHSteCs. This finding was confirmed by induction of irreversible cell?cycle arrest, upregulation of 53BP1 and p21 expression, and increased SA?β?gal staining. Senescent HHSteCs released increased quantities of EV particles compared with normally cultured HHSteCs. Multiplex analysis revealed that there was no difference between hepatoma cell lines treated with normal EVs and those treated with senescent EVs in growth factor secretion. In contrast, the secretion of epidermal growth factor (EGF) was increased by macrophage cells treated with senescent EVs compared with those treated with normal EVs. Furthermore, senescent EVs did not affect the viability of hepatoma cells but increased the viability of hepatoma cells co?cultured with macrophage cells. In conclusion, the release of EVs from senescent HSCs was higher compared with normal HSCs. Furthermore, senescent EVs promoted HCC development by upregulating EGF secretion from macrophages.
長崎大学学位論文学位記番号:博(医歯薬)甲第1274号学位授与年月日:令和2年9月2日
Author: Yuri Miyazoe, Satoshi Miuma, Hisamitsu Miyaaki, Yasuko Kanda, Suguru Nakashiki, Ryu Sasaki, Masafumi Haraguchi, Hidetaka Shibata, Takuya Honda, Naota Taura, Kazuhiko Nakao
Citation: Biomedical Reports, 12(4), pp.163-170, 2020
identifier:Nagasaki University (長崎大学), 博士(医学) (2020-09-02)
Source: comment：fulltext
https://nagasaki-u.repo.nii.ac.jp/?action=repository_action_common_download&item_id=53&item_no=1&attribute_id=70&file_no=1
Access Restrictions: インターネット公開
Rights (production): c Miyazoe et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
Related Material: http://hdl.handle.net/10069/40345
Related Material (DOI): 10.3892/br.2020.1279
Data Provider (Database): 国立情報学研究所 : 学術機関リポジトリデータベース（IRDB）（機関リポジトリ）
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Original Data Provider (Database): 長崎大学 : 長崎大学学術研究成果リポジトリ