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In vitro generation of functional dendritic cells differentiated from CD34 negative cells isolated from human umbilical cord blood
Author(s) -
Park Yo Seph,
Shin Changsik,
Hwang Han Sung,
Zenke Martin,
Han Dong Wook,
Kang Young Sun,
Ko Kisung,
Do Yoonkyung,
Ko Kinarm
Publication year - 2015
Publication title -
cell biology international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.932
H-Index - 77
eISSN - 1095-8355
pISSN - 1065-6995
DOI - 10.1002/cbin.10490
Subject(s) - cd34 , cell sorting , haematopoiesis , microbiology and biotechnology , dendritic cell , cord blood , stem cell , immunology , antigen , umbilical cord , population , biology , immune system , chemistry , flow cytometry , medicine , environmental health
Dendritic cells (DCs) are the most potent antigen‐presenting cells that play a crucial role in the initiation of an immune response. As DC‐based therapeutic applications is increasing, large‐scale DC production is required for transplantation. Human umbilical cord blood (UCB) has been shown to contain a rare and precious population of hematopoietic stem cells (HSCs), which can give rise to DCs. The CD34 antigen has been widely used as a cell surface marker to identify HSCs. In this study, we used CD34 antibody to isolate CD34 + and CD34 − cells and compared the ability to differentiate into DCs. We used a two‐step method combined with the magnetic bead sorting system to isolate CD34 + and CD34 − cells from human UCB. Analysis of cellular properties and functionality using a migration assay and T cell proliferation assay revealed no significant differences between CD34 + cells and CD34 − cells in their ability to generate DCs.