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Hassan, Ghmkin Graduate School of Interdisciplinary Science and Engineering in Health Systems, Okayama University ORCID publons
Afify, Said M. Graduate School of Interdisciplinary Science and Engineering in Health Systems, Okayama University ORCID
Nair, Neha Graduate School of Natural Science and Technology, Okayama University
Kumon, Kazuki Graduate School of Natural Science and Technology, Okayama University
Osman, Amira Graduate School of Interdisciplinary Science and Engineering in Health Systems, Okayama University
Du, Juan Graduate School of Natural Science and Technology, Okayama University
Mansour, Hager
Abu Quora, Hagar A. Graduate School of Interdisciplinary Science and Engineering in Health Systems, Okayama University
Nawara, Hend M. Graduate School of Natural Science and Technology, Okayama University
Satoh, Ayano Graduate School of Interdisciplinary Science and Engineering in Health Systems, Okayama University ORCID Kaken ID publons researchmap
Zahra, Maram H. Graduate School of Interdisciplinary Science and Engineering in Health Systems, Okayama University
Okada, Nobuhiro Graduate School of Interdisciplinary Science and Engineering in Health Systems, Okayama University
Seno, Akimasa Graduate School of Interdisciplinary Science and Engineering in Health Systems, Okayama University ORCID Kaken ID publons researchmap
Seno, Masaharu Graduate School of Interdisciplinary Science and Engineering in Health Systems, Okayama University ORCID Kaken ID publons researchmap
Abstract
Cancer stem cells (CSCs) represent the subpopulation of cancer cells with the ability to differentiate into other cell phenotypes and initiated tumorigenesis. Previously, we reported generating CSCs from mouse induced pluripotent stem cells (miPSCs). Here, we investigated the ability of the CSCs to differentiate into hematopoietic cells. First, the primary cells were isolated from malignant tumors that were formed by the CSCs. Non-adherent cells (NACs) that arose from adherent cells were collected and their viability, as well as the morphology and expression of hematopoietic cell markers, were analyzed. Moreover, NACs were injected into the tail vein of busulfan conditioned Balb/c nude mice. Finally, CSCs were induced to differentiate to macrophages while using IL3 and SCF. The round nucleated NACs were found to be viable, positive for hematopoietic lineage markers and CD34, and expressed hematopoietic markers, just like homing to the bone marrow. When NACs were injected into mice, Wright-Giemsa staining showed that the number of white blood cells got higher than those in the control mice after four weeks. CSCs also showed the ability to differentiate toward macrophages. CSCs were demonstrated to have the potential to provide progenies with hematopoietic markers, morphology, and homing ability to the bone marrow, which could give new insight into the tumor microenvironment according to the plasticity of CSCs.
Keywords
Induced pluripotent stem cells
Cancer stem cells differentiation
tumor microenvironment
hematopoietic cells
Published Date
2019-12-29
Publication Title
Cancers
Volume
volume12
Issue
issue1
Publisher
MDPI
Start Page
82
ISSN
2072-6694
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
Copyright Holders
© 2019 by the authors.
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publisher
PubMed ID
DOI
Web of Science KeyUT
Related Url
isVersionOf https://doi.org/10.3390/cancers12010082
License
http://creativecommons.org/licenses/by/4.0/
Funder Name
Ministry of Education, Culture, Sports, Science and Technology
助成番号
25242045
18K15243