Summary of ssbd-repos-00024

SSBD:database
URL

Name
ssbd-repos-00024 (24-Kanemura-iPSCellDyn)
URL
DOI
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Title
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Description
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Submited Date
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Release Date
2017-10-03
Updated Date
2018-11-15
License
Funding information
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File formats
Data size
10.5 MB

Organism
H. sapiens
Strain
iPS
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)
NA
GO Cellular Component (CC)
cell
Study Type
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Imaging Methods
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Method Summary
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Related paper(s)

Hoshimi Kanemura, Masahiro J Go, Naoki Nishishita, Noriko Sakai, Hiroyuki Kamao, Yoji Sato, Masayo Takahashi, Shin Kawamata (2013) Pigment epithelium-derived factor secreted from retinal pigment epithelium facilitates apoptotic cell death of iPSC., Scientific reports, Volume 3, pp. 2334

Published in 2013

(Abstract) We show that pigment epithelium-derived factor (PEDF), which is secreted from primary or iPSC-derived retinal pigment epithelium (RPE), dramatically inhibits the growth of iPSCs. PEDF is detected abundantly in culture supernatants of primary or iPSC-derived RPE. Apoptotic cell death is induced in iPSC when co-cultured with RPE, a process that is significantly blocked by addition of antibody against PEDF. Indeed, addition of recombinant PEDF to the iPSC cell culture induces apoptotic cell death in iPSCs, but the expression of pluripotency related-genes is maintained, suggesting that PEDF causes cell death, not differentiation, of iPSCs. To recapitulate this event in vivo, we examined tumor formation in NOG mice after subcutaneous injection of iPSCs with or without an iPSC-derived RPE sheet (2.5 x 10(5) RPE cells). We observed that the tumor forming potential of iPSCs was significantly suppressed by simultaneous transplantation with an iPSC-derived RPE sheet.
(MeSH Terms)

Contact(s)
Shin Kawamata
Organization(s)
Foundation for Biomedical Research and Innovation , Research & Development Center for Cell Therapy , Laboratory for Retinal Regeneration
Image Data Contributors
Quantitative Data Contributors

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