Please use this identifier to cite or link to this item: https://doi.org/10.1002/sctm.17-0251
Title: Ex Vivo Expansion of CD34+CD90+CD49f+ Hematopoietic Stem and Progenitor Cells from Non-Enriched Umbilical Cord Blood with Azole Compounds
Authors: Bari, S. 
Zhong, Q. 
Fan, X.
Poon, Z.
Lim, A.S.T.
Lim, T.H.
Dighe, N.
Li, S.
Chiu, G.N.C. 
Chai, C.L.L. 
Hwang, W.Y.K.
Keywords: Azole-based small molecules
Ex vivo expansion
Hematopoietic stem and progenitor cells
Hematopoietic stem cell transplantation
Umbilical cord blood
Xenotransplantation with immunodeficient mouse model
Issue Date: 2018
Publisher: John Wiley and Sons Ltd.
Citation: Bari, S., Zhong, Q., Fan, X., Poon, Z., Lim, A.S.T., Lim, T.H., Dighe, N., Li, S., Chiu, G.N.C., Chai, C.L.L., Hwang, W.Y.K. (2018). Ex Vivo Expansion of CD34+CD90+CD49f+ Hematopoietic Stem and Progenitor Cells from Non-Enriched Umbilical Cord Blood with Azole Compounds. Stem Cells Translational Medicine 7 (5) : 376-393. ScholarBank@NUS Repository. https://doi.org/10.1002/sctm.17-0251
Rights: Attribution-NonCommercial-NoDerivatives 4.0 International
Abstract: Umbilical cord blood (UCB) transplants in adults have slower hematopoietic recovery compared to bone marrow (BM) or peripheral blood (PB) stem cells mainly due to low number of total nucleated cells and hematopoietic stem and progenitor cells (HSPC). As such in this study, we aimed to perform ex vivo expansion of UCB HSPC from non-enriched mononucleated cells (MNC) using novel azole-based small molecules. Freshly-thawed UCB–MNC were cultured in expansion medium supplemented with small molecules and basal cytokine cocktail. The effects of the expansion protocol were measured based on in vitro and in vivo assays. The proprietary library of >50 small molecules were developed using structure-activity-relationship studies of SB203580, a known p38-MAPK inhibitor. A particular analog, C7, resulted in 1,554.1 ± 27.8-fold increase of absolute viable CD45+CD34+CD38–CD45RA– progenitors which was at least 3.7-fold higher than control cultures (p <.001). In depth phenotypic analysis revealed >600-fold expansion of CD34+/CD90+/CD49f+ rare HSPCs coupled with significant (p <.01) increase of functional colonies from C7 treated cells. Transplantation of C7 expanded UCB grafts to immunodeficient mice resulted in significantly (p <.001) higher engraftment of human CD45+ and CD45+CD34+ cells in the PB and BM by day 21 compared to non-expanded and cytokine expanded grafts. The C7 expanded grafts maintained long-term human multilineage chimerism in the BM of primary recipients with sustained human CD45 cell engraftment in secondary recipients. In conclusion, a small molecule, C7, could allow for clinical development of expanded UCB grafts without pre-culture stem cell enrichment that maintains in vitro and in vivo functionality. Stem Cells Translational Medicine 2018;7:376–393. © 2018 The Authors Stem Cells Translational Medicine published by Wiley Periodicals, Inc. on behalf of AlphaMed Press
Source Title: Stem Cells Translational Medicine
URI: https://scholarbank.nus.edu.sg/handle/10635/212552
ISSN: 2157-6564
DOI: 10.1002/sctm.17-0251
Rights: Attribution-NonCommercial-NoDerivatives 4.0 International
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