ID | 61045 |
著者 |
Osman, Amira
Laboratory of Nano-Biotechnology, Graduate School of Interdisciplinary Science and Engineering in Health Systems
Oze, Miharu
Department of Medical Bioengineering, Graduate School of Natural Science and Technology
Afify, Said M.
Laboratory of Nano-Biotechnology, Graduate School of Interdisciplinary Science and Engineering in Health Systems
ORCID
Hassan, Ghmkin
Laboratory of Nano-Biotechnology, Graduate School of Interdisciplinary Science and Engineering in Health Systems
ORCID
publons
EL-Ghlban, Samah
Laboratory of Nano-Biotechnology, Graduate School of Interdisciplinary Science and Engineering in Health Systems, Okayama University
Nawara, Hend M.
Department of Medical Bioengineering, Graduate School of Natural Science and Technology, Okayama University
Fu, Xiaoying
Laboratory of Nano-Biotechnology, Graduate School of Interdisciplinary Science and Engineering in Health Systems, Okayama University
Zahra, Maram Hussein
Laboratory of Nano-Biotechnology, Graduate School of Interdisciplinary Science and Engineering in Health Systems, Okayama University
Seno, Akimasa
Laboratory of Nano-Biotechnology, Graduate School of Interdisciplinary Science and Engineering in Health Systems, Okayama University
ORCID
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researchmap
Winer, Ira
Department of Obstetrics & Gynecology, School of Medicine, Wayne State University
Salomon, David S.
Mouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute
Seno, Masaharu
Laboratory of Nano-Biotechnology, Graduate School of Interdisciplinary Science and Engineering in Health Systems, Okayama University
ORCID
Kaken ID
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researchmap
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抄録 | Macrophages are the most abundant immune cells in the microenvironment of solid tumors. The present study displayed histological and immunohistochemical analyses of a malignant tumor model developed from cancer stem cells (CSCs) converted from human induced pluripotent stem cells (hiPSCs) in a cancer microenvironment prepared from the conditioned medium (CM) of a pancreatic cancer cell line. We focused on the localization and the origin of tumor-associated macrophages (TAMs), To the best of our knowledge this may be the first study to suggest the potential differentiation of CSCs to TAMs.hiPSCs were converted into CSCs in the presence of CM from PK8 cells. CSCs were then transplanted in vivo and formed primary tumors. Primary cultures for these tumors were serially transplanted again to obtain secondary tumors. Secondary tumors exhibited histopathological features of malignancy. Cells derived from tumors maintained the expression of endogenous stemness markers and pancreatic CSCs markers. Simultaneously, high immunoreactivity to anti-mouse CD68, anti-human CD68, CD206 and CD11b antibodies were detected revealing that the tumor tissue derived from CSCs was enriched for macrophages which can originate from both human and mouse cells.The model of CSCs highlighted the possibility of CSCs to differentiate into TAMs.
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キーワード | TAMs
TME
hiPSCs
Anti-CD antibodies
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備考 | This fulltext is available in September, 2021.
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発行日 | 2020-12-31
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出版物タイトル |
Acta Histochemica
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巻 | 122巻
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号 | 8号
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出版者 | Elsevier
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開始ページ | 151628
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ISSN | 0065-1281
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NCID | AA00508000
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資料タイプ |
学術雑誌論文
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言語 |
English
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OAI-PMH Set |
岡山大学
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論文のバージョン | author
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PubMed ID | |
DOI | |
Web of Science KeyUT | |
関連URL | isVersionOf https://doi.org/10.1016/j.acthis.2020.151628
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ライセンス | https://creativecommons.org/licenses/by-nc-nd/4.0/
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