Summary of ssbd-repos-000318

SSBD:database
URL

Name
ssbd-repos-000318 (318-Yamamoto-StemCell)
URL
DOI
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Title
Human adipose mesenchymal stem cells
Description
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Submited Date
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Release Date
2024-12-14
Updated Date
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License
Funding information
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File formats
Data size
73.7 MB

Organism
Homo sapiens
Strain
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Cell Line
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Genes
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Proteins
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GO Molecular Function (MF)
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GO Biological Process (BP)
cell population proliferation
GO Cellular Component (CC)
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Study Type
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Imaging Methods
light microscopy

Method Summary
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Related paper(s)

Takako Yamamoto, Mao Arita, Takashi Tamura, Miho Saito, Hirohito Katayama, Hirotaka Kuroda, Takashi Suzuki, Shin Kawamata (2023) A Novel Approach for Determining the Critical Quality Attributes of Mesenchymal Stem Cells by Specifying Cell Population With Replication Potential., Stem cells translational medicine, Volume 12, Number 3, pp. 169-182

Published in 2023 Mar 17

(Abstract) We introduce a novel approach to determine the critical quality attributes (CQAs) of mesenchymal stem cells (MSCs) expected to exert immunosuppressive effects. MSCs retained homeostatic replication potentials, such as sustainable growth and consistent cell morphology as a population, in early passages, but lost them in late passages. Characteristic surface markers of MSCs (ie, CD73, CD90, and CD105) were no longer expressed at 2 weeks after subcutaneous transplantation into NOG mice when MSCs from late passages were transplanted, but not when MSCs from early passages were transplanted, suggesting that the biological effects of the MSCs differed according to the timing of cell harvesting and highlighting the importance of specifying MSCs that retained homeostatic features to define the CQAs. The homeostatic features of MSCs related to the balance of the redox system, nutrient requirements, and mitochondrial function were also observed until a certain passage. Therefore, we could define the CQAs of MSCs related to manufacturing by selecting process parameters (PPs) underlying the homeostatic features of MSCs and measuring these PPs quantitatively to specify the cell population with homeostatic features by limiting the passage number. The validity of the PPs stipulated in our pilot study was verified using an SKG murine arthritis model, and critical PPs (CPPs) were then selected among the PPs. Thus, CQAs related to manufacturing in the developmental phase could be defined by the CPPs in this manner, and the concept of CQAs could be refined continuously toward commercial manufacturing.
(MeSH Terms)

Contact(s)
Shin Kawamata
Organization(s)
Kobe University, Cyto-Facto Inc. , Graduate School of Science, Technology and Innovation
Image Data Contributors
Quantitative Data Contributors

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