生物
造血
祖细胞
川地34
干细胞
脐带血
细胞生物学
免疫学
移植
人口
CD90型
造血干细胞
离体
体内
生物技术
内科学
人口学
社会学
医学
作者
Marina Tarunina,Diana Hernandez,Barbara Kronsteiner,Philip Pratt,Thomas Watson,Hua Peng,Francesca Gullo,Mark van der Garde,Youyi Zhang,Lilian Hook,Yen Choo,Suzanne M. Watt
出处
期刊:Stem Cells and Development
[Mary Ann Liebert, Inc.]
日期:2016-08-24
卷期号:25 (22): 1709-1720
被引量:12
标识
DOI:10.1089/scd.2016.0216
摘要
The main limitations of hematopoietic cord blood (CB) transplantation, viz, low cell dosage and delayed reconstitution, can be overcome by ex vivo expansion. CB expansion under conventional culture causes rapid cell differentiation and depletion of hematopoietic stem and progenitor cells (HSPCs) responsible for engraftment. In this study, we use combinatorial cell culture technology (CombiCult®) to identify medium formulations that promote CD133+ CB HSPC proliferation while maintaining their phenotypic characteristics. We employed second-generation CombiCult screens that use electrospraying technology to encapsulate CB cells in alginate beads. Our results suggest that not only the combination but also the order of addition of individual components has a profound influence on expansion of specific HSPC populations. Top protocols identified by the CombiCult screen were used to culture human CD133+ CB HSPCs on nanofiber scaffolds and validate the expansion of the phenotypically defined CD34+CD38lo/-CD45RA-CD90+CD49f+ population of hematopoietic stem cells and their differentiation into defined progeny.
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