The role of poloxamer 188 for cord blood mononuclear cells into megakaryocytes cultivation and induction in three-dimensional WAVE Bioreactor
10.3760/cma.j.issn.0253-2727.2018.01.006
- VernacularTitle: 泊洛沙姆188对体外三维培养脐血单个核细胞向巨核细胞分化的影响
- Author:
Lin CHEN
1
,
2
;
Wen YUE
;
Xiaoyan XIE
;
Xiuyuan ZHANG
;
Yang LYU
;
Daqing LIU
;
Jiafei XI
;
Mingyi QU
;
Zeng FAN
;
Fang FANG
;
Xuantao PEI
Author Information
1. Stem Cell and Regenerative Medicine Lab, Beijing Institute of Transfusion Medicine, Beijing 100850, China
2. South China Institute of Biomedicine, Guangzhou 510005, China
- Publication Type:Journal Article
- Keywords:
Megakaryocytes;
Poloxamer;
Bioreactors;
Differentiation
- From:
Chinese Journal of Hematology
2018;39(1):28-31
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To observe the effect of poloxamer 188 (P188) on megakaryocyte cultivation and induction from cord blood mononuclear cells in order to obtain more megakaryocyte progenitor cells (MPC).
Methods:The cord blood mononuclear cells were isolated and inoculated in cell culture bag or cell culture flask respectively. The WIGGENS shaker and cell culture bags were used to mimick WAVE Bioreactor for three-dimensional (3D) cell culture, and the P188 was added to induction medium, The cells were detected for morphology, surface marker, viability, and number on day 14.
Results:In the two-dimensional (2D) culture, CD41+, CD41+/CD61+, CD61+ megakaryocytic numbers increased significantly after adding P188 (all P<0.01). And in the 3D culture of adding P188, the cell volume became larger and the nuclear shape was irregular, the cytoplasm appeared magenta granules, and the megakaryocyte cells became more mature. By 3D culture, the expression of CD41/CD61 was (36.30±1.27)% vs (23.95±1.34)%, hence the differentiation for MPC was significantly higher than that in the 2D group (P<0.01). Furthermore, adding P188 in 3D culture resulted in highest differentiation efficiency for MPC [(59.45±1.20)%]. There were no significantly differences in terms of cell viability and cell number among 3D culture containing P188, 2D and 3D culture groups (all P>0.05).
Conclusion:3D culture was beneficial for the differentiation of MPC, but the cell viability was lower than 2D group; However, the satisfied cell growth and better induction efficiency were obtained by adding of P188, which might provide a new method of megakaryocytes production for clinical application.
