2014 Fiscal Year Annual Research Report
HHIP KOストローマ細胞を用いたドナー由来リンパ球インビトロ増幅法の開発
Project/Area Number |
24591427
|
Research Institution | Sapporo Medical University |
Principal Investigator |
井山 諭 札幌医科大学, 医学部, 助教 (50398319)
|
Co-Investigator(Kenkyū-buntansha) |
神原 悠輔 札幌医科大学, 医学部, 研究員 (10624421)
加藤 淳二 札幌医科大学, 医学部, 教授 (20244345)
小船 雅義 札幌医科大学, 医学部, 准教授 (90336389)
|
Project Period (FY) |
2012-04-01 – 2015-03-31
|
Keywords | リンパ球増幅 |
Outline of Annual Research Achievements |
We have previously shown that it was difficult to evaluate 5 weeks CA-forming cells (CAFC) which is a surrogate indicator of hematopoietic stem cells because human stromal cells could not survive more than 4 weeks. In this study, we optimized surum free media, combination of cytokines and chemical agents such as stem cell factor, thrombopoietin, flt3 ligand with or without delta like protein 4 (DLL4) and GSK inhibitor. By using this media, bone marrow CD34+ cells could be cocultured for 8 weeks without disruption of the human stromal layer. Five week CAFC could be observed in all condition of cytokine combination with or without chemical inhibitor. However, because cytoplasmic appearance of cells in some CAs is quite irregular without DLL4 or GSK inhibitor, we conducted immunohistochemical staining. We found that CD34+CAFCs were exclusively observed in the presence of DLL4 or GSK inhibitor. Moreover, NOD/SCID repopulating cells were detected in the coculture containing CD34+CAFCs.
|
Research Products
(3 results)
-
-
[Journal Article] Efficacy of Enteral Supplementation Enriched with Glutamine, Fiber, and Oligosaccharide on Mucosal Injury following Hematopoietic Stem Cell Transplantation2014
Author(s)
Iyama S, Sato T, Tatsumi H, Hashimoto A, Tatekoshi A, Kamihara Y, Horiguchi H, Ibata S, Ono K, Murase K, Takada K, Sato Y, Hayashi T, Miyanishi K, Akizuki E, Nobuoka T, Mizuguchi T, Takimoto R, Kobune M, Hirata K, Kato J.
-
Journal Title
Case Rep Oncol
Volume: 7
Pages: 692-699
DOI
Peer Reviewed / Open Access / Acknowledgement Compliant
-
[Presentation] Exosomes Derived from AML/MDS Cells Is Involved in Stromal Dysfunction and Bone Marrow Failure.2014
Author(s)
Horiguchi H, Kobune M, Kikuchi S, Jomen W, Murase K, Ibata S, Iyama S, Sato T, Kamihara Y, Miyanishi K, Sato Y, Hayashi T, Takimoto R, Kato J.
Organizer
56th ASH Annual Meeting and Exposition
Place of Presentation
San Francisco, U.S.A
Year and Date
2014-12-06 – 2014-12-09